Full data view for gene COL3A1

Ehlers Danlos Syndrome Variant Database


Information The variants shown are described using the NM_000090.3 transcript reference sequence.

1810 entries on 19 pages. Showing entries 1 - 100.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Predicted     

Type/DNA     

Legacy protein change     

Allele     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+/. _1_51_ c.-107_*972{0} r.0 p.0 - - - Unknown - pathogenic (dominant) g.(188405810_188498336)_(200267551_200275296)del - 2q deletion - COL3A1_000963 - - - - Germline/De novo (untested) - - - - - DNA arrayCGH - blood EDSVASC 86 - Proband F - United Kingdom (Great Britain) - - - - - 1 Duncan Baker
+/. _1_51_ c.-107_*972{0} r.0 p.0 - - - Unknown - pathogenic (dominant) g.(g.(?_186534129)_(202840810_?)del - 2q deletion - COL3A1_000963 - - - - Germline/De novo (untested) - - - - - DNA arrayCGH - blood EDSVASC 96 - Proband F - United Kingdom (Great Britain) - - - - - 1 Duncan Baker
+/. _1_51_ c.-107_*972{0} r.0 p.0 - - - Unknown - pathogenic (dominant) g.(?_186408968)_(201568314_?)del - 2q deletion - COL3A1_000963 - - - - De novo - - - - - DNA arrayCGH - blood EDSVASC 99 - proband F - United Kingdom (Great Britain) - - - - - 1 Duncan Baker
+/. _1_51_ c.-107_*972{0} r.0 p.0 - - - Unknown - pathogenic (dominant) g.(185139669_185234253)_(214491747_214548932)del - 2q deletion - COL3A1_000963 - - - - De novo - - - - - DNA arrayCGH - amniotic fluid EDSVASC 137 - proband F - United Kingdom (Great Britain) - - - - - 1 Duncan Baker
+/+ 1-52 c.1-?_c.4401+?del r.? - deletion, multi exon deletion - Unknown - pathogenic g.(?_189839099)_(189877472_?)del - - - COL3A1_000620 - PubMed: Frank et al., 2015 - - Unknown - - - - - DNA SEQ - - EDS, EDSVASC - PubMed: Frank et al., 2015 - - - - - - - - - 1 Xavier Jeunemaitre
?/. - c.3G>A r.(?) p.(Met1?) - - - Unknown - VUS g.189839218G>A g.188974492G>A - - COL3A1_000870 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/+ 1 c.30G>A r.? p.(Trp10*) nonsense substitution - Maternal (confirmed) - pathogenic g.189839245G>A - - - COL3A1_000373 - PubMed: Pepin et al., 2014 - - Unknown - - - - - DNA, RNA PCR, PCR, RT-PCR, SEQ - - EDS, EDSVASC - PubMed: Pepin et al., 2014 - - - - - - - - - 1 Peter Byers
-?/. - c.80-226G>C r.(=) p.(=) - - - Unknown - likely benign g.189849260G>C - COL3A1(NM_000090.4):c.80-226G>C - COL3A1_001024 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.80-59C>T r.(=) p.(=) - - - Unknown - likely benign g.189849427C>T - COL3A1(NM_000090.4):c.80-59C>T - COL3A1_000809 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.80-22C>T r.(=) p.(=) - - - Unknown - likely benign g.189849464C>T g.188984738C>T COL3A1(NM_000090.3):c.80-22C>T - COL3A1_000817 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-/. - c.80-16C>T r.(=) p.(=) - - - Unknown - benign g.189849470C>T g.188984744C>T COL3A1(NM_000090.3):c.80-16C>T, COL3A1(NM_000090.4):c.80-16C>T - COL3A1_000818 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.80-16C>T r.(=) p.(=) - - - Unknown - likely benign g.189849470C>T - COL3A1(NM_000090.3):c.80-16C>T, COL3A1(NM_000090.4):c.80-16C>T - COL3A1_000818 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.87A>C r.(?) p.(Glu29Asp) - - - Unknown - likely benign g.189849493A>C g.188984767A>C COL3A1(NM_000090.3):c.87A>C (p.E29D) - COL3A1_000819 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.111G>A r.(?) p.(Gln37=) - - - Unknown - likely benign g.189849517G>A g.188984791G>A COL3A1(NM_000090.4):c.111G>A (p.Q37=) - COL3A1_000801 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.113C>A r.(?) p.(Ser38Tyr) - - - Unknown - VUS g.189849519C>A g.188984793C>A COL3A1(NM_000090.3):c.113C>A (p.S38Y) - COL3A1_000802 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.114C>G r.(?) p.(Ser38=) - - - Unknown - likely benign g.189849520C>G g.188984794C>G COL3A1(NM_000090.3):c.114C>G (p.S38=), COL3A1(NM_000090.4):c.114C>G (p.S38=) - COL3A1_000820 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.114C>G r.(?) p.(Ser38=) - - - Unknown - likely benign g.189849520C>G g.188984794C>G COL3A1(NM_000090.3):c.114C>G (p.S38=), COL3A1(NM_000090.4):c.114C>G (p.S38=) - COL3A1_000820 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.114C>G r.(?) p.(Ser38=) - - - Unknown - likely benign g.189849520C>G g.188984794C>G COL3A1(NM_000090.3):c.114C>G (p.S38=), COL3A1(NM_000090.4):c.114C>G (p.S38=) - COL3A1_000820 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.119C>A r.(?) p.(Ala40Glu) - - - Unknown - likely benign g.189849525C>A g.188984799C>A - - COL3A1_000887 analysis 8380 WGS samples Japan PubMed: Shido 2021 - rs201380807 CLASSIFICATION record - 0.0008 - - - - - - - - - - - - - - - - - - - - -
-/- 2 c.119C>T r.? p.(Ala40Val) missense substitution - Unknown - likely benign g.189849525C>T - - - COL3A1_000746 - PubMed: Sakai et al., 2011 - - Unknown - - - - - DNA SEQ-NG, PCRm, PCR, arraySEQ - - ? - PubMed: Sakai et al., 2011 The technique used was the custom NGS Gene panel. - - - - - - - - 1 Raymond Dalgleish
?/. - c.121G>T r.(?) p.(Asp41Tyr) - - - Unknown - VUS g.189849527G>T - COL3A1(NM_000090.4):c.121G>T (p.D41Y) - COL3A1_000988 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.123T>C r.(?) p.(Asp41=) - - - Unknown - likely benign g.189849529T>C - COL3A1(NM_000090.3):c.123T>C (p.D41=) - COL3A1_000894 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/+? 2 c.130G>A r.? p.(Val44Ile) missense substitution - Unknown - likely pathogenic g.189849536G>A - - - COL3A1_000587 - PubMed: Frank et al., 2015 - - Unknown - - - - - DNA SEQ - - EDS, EDSVASC - PubMed: Frank et al., 2015 - - - - - - - - - 1 Xavier Jeunemaitre
-?/. - c.130G>A r.(?) p.(Val44Ile) - - - Unknown - likely benign g.189849536G>A - COL3A1(NM_000090.4):c.130G>A (p.V44I) - COL3A1_000587 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/+ 2 c.145C>G r.? p.(Pro49Ala) missense substitution - Both (homozygous) - pathogenic g.189849551C>G - - - COL3A1_000646 - PubMed: Vandervore et al., 2017 - - Unknown - - - - - DNA PCR, SEQ, SEQ-NG - - ? Patient 1 PubMed: Vandervore et al., 2017 The proband's younger brother is also homozygous for this variant. The heterozygous parents are healthy.The technique used was whole exome sequencing. - - - Chechnyan - - - - 1 Raymond Dalgleish
+/+ 2 c.145C>G r.? p.(Pro49Ala) missense substitution - Both (homozygous) - pathogenic g.189849551C>G - - - COL3A1_000646 - PubMed: Horn et al., 2017 - - Unknown - - - - - DNA SEQ - - ? Patient 2 PubMed: Horn et al., 2017 The patient's younger brother is also homozygous for the variant. Both parents were heterozygous carriers of the variant. These patients are distinct from those in PubMed: Vandervore et al., 2017 - - - - - - - - 1 Raymond Dalgleish
-?/. - c.186C>T r.(?) p.(Cys62=) - - - Unknown - likely benign g.189849592C>T g.188984866C>T COL3A1(NM_000090.3):c.186C>T (p.C62=), COL3A1(NM_000090.4):c.186C>T (p.C62=) - COL3A1_000821 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.186C>T r.(?) p.(Cys62=) - - - Unknown - likely benign g.189849592C>T g.188984866C>T COL3A1(NM_000090.3):c.186C>T (p.C62=), COL3A1(NM_000090.4):c.186C>T (p.C62=) - COL3A1_000821 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+?/. - c.190G>T r.(?) p.(Asp64Tyr) missense substitution - Both (homozygous) ACMG VUS g.189849596G>T g.188984870G>T - - COL3A1_000962 - - - - Germline yes - - - - DNA SEQ-NG-I - - epilepsy - - - - yes Pakistan - - - - - 1 Sadaf Naz
+?/+? 2 c.194_195dup r.? p.(Ile66*) frameshift duplication - Unknown - likely pathogenic g.189849600_189849601dup - - - COL3A1_000693 - PubMed: Legrand et al., 2019 - - Unknown - - - - - DNA PCR, SEQ - - EDS, EDSVASC - PubMed: Legrand et al., 2019 - - - - - - - - - 1 Raymond Dalgleish
-?/-? 2 c.198A>G r.? p.(Ile66Met) missense substitution - Unknown - benign g.189849604A>G - - - COL3A1_000631 - - - - Unknown - - - - - DNA SEQ-NG - - EDS, EDSHMB - - Hypermobility EDS / BJHS: EDS III Benign connective tissue phenotype with coronary artery dissections. - - - white - - - - 1 Ruwan Weerakkody
+/+ 2 c.202_207del r.? p.(Asp68_Asp69del) deletion deletion - Unknown - pathogenic g.189849608_189849613del - - - COL3A1_000340 - PubMed: Frank et al., 2015 - - Unknown - - - - - DNA SEQ - - EDS, EDSVASC - PubMed: Frank et al., 2015 This patient was subsequently described in PubMed: Legrand et al., 2019. - - - - - - - - 1 Xavier Jeunemaitre
./. - c.217G>C r.(?) p.(Asp73His) - - - Unknown - likely pathogenic g.189849623G>C g.188984897G>C NM_000090.3(COL3A1):c.217G>C p.(Asp73His) - COL3A1_000816 variant could not be associated with disease phenotype PubMed: Vogelaar 2017, Journal: Vogelaar 2017 - - Germline - - - - - DNA SEQ-NG - - cancer, gastric Vogelaar-529A PubMed: Vogelaar 2017, Journal: Vogelaar 2017 54 patients from 53 families with genetically unexplained diffuse-type and intestinal-type gastric cancer - - - - - - - - 1 Marjolijn JL Ligtenberg
?/. - c.217G>C r.(?) p.(Asp73His) - - - Unknown - VUS g.189849623G>C g.188984897G>C COL3A1(NM_000090.3):c.217G>C (p.D73H) - COL3A1_000816 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.225C>A r.(?) p.(=) - - - Unknown - likely benign g.189849631C>A - COL3A1(NM_000090.4):c.225C>A (p.P75=) - COL3A1_001062 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.318_325del r.(?) p.(Pro107ArgfsTer13) - - - Unknown - pathogenic g.189849958_189849965del g.188985232_188985239del COL3A1(NM_000090.4):c.318_325delCCCCAAGG (p.P107Rfs*13) - COL3A1_000648 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/+ 3 c.318_325del r.? p.(Pro107Argfs*13) frameshift deletion - Unknown - pathogenic g.189849958_189849965del - - - COL3A1_000648 - PubMed: Overwater et al., 2018 - - Unknown - - - - - DNA SEQ-NG - - EDS, EDSVASC Pat9 PubMed: Overwater 2018 The technique used was the custom NGS Gene panel. - - Netherlands - - - - - 1 Alessandra Maugeri
-?/. - c.333+15T>C r.(=) p.(=) - - - Unknown - likely benign g.189849988T>C - COL3A1(NM_000090.4):c.333+15T>C - COL3A1_000895 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.334-97G>A r.(=) p.(=) - - - Unknown - likely benign g.189850294G>A - COL3A1(NM_000090.4):c.334-97G>A - COL3A1_001009 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. 3i c.334-11C>G r.spl? p.(?) - - - Unknown - VUS g.189850380C>G g.188985654C>G - - COL3A1_000964 - Leone 2023, submitted - - Germline - - - - - DNA SEQ, SEQ-NG blood - ? P-0189 Leone 2023, submitted - - - Italy - - - - - 1 Maria Pia Leone
?/. - c.370G>C r.(?) p.(Gly124Arg) - - - Unknown - VUS g.189850427G>C g.188985701G>C COL3A1(NM_000090.4):c.370G>C (p.G124R) - COL3A1_000653 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/? 4_5 c.370G>C r.? p.(Gly124Arg) missense substitution - Unknown - VUS g.189850427G>C - - - COL3A1_000653 - - - - Unknown - - - - - DNA SEQ-NG - - ? - - The technique used was the custom NGS Gene panel. - - - - - - - - 1 Alessandra Maugeri
?/. - c.370G>C r.(?) p.(Gly124Arg) - - - Parent #1 - VUS g.189850427G>C g.188985701G>C - - COL3A1_000653 - PubMed: Overwater 2018 - - Germline yes 1/128 cases FA - - - DNA SEQ, SEQ-NG - gene panel ? Pat69 PubMed: Overwater 2018 - - - Netherlands - - - - - 1 Johan den Dunnen
+/+ - c.382C>T r.(?) p.(Gln128*) nonsense substitution - Unknown - pathogenic g.189850439C>T g.188985713C>T - - COL3A1_000943 - - - - Germline - - - - - DNA SEQ-NG Blood - EDSVASC 42* - - M - - - - - - - 2 Duncan Baker
+/+ 4_5 c.413del r.? p.(Pro138Leufs*27) frameshift deletion - Unknown - pathogenic g.189850470del - - - COL3A1_000125 - PubMed: Schwarze et al., 2001 PubMed: Pepin et al., 2014 - - Unknown - - - - - DNA PCR, SEQ - - EDS, EDSVASC - PubMed: Schwarze et al., 2001 PubMed: Pepin et al., 2014 The patient was described by PubMed: Schwarze et al., 2001 as patient P2. The patient was subsequently presented as Family 1 by PubMed: Leistritz et al., 2011. - - - - - - - - 1 Peter Byers
-?/. - c.447+13C>T r.(=) p.(=) - - - Unknown - likely benign g.189850517C>T - COL3A1(NM_000090.3):c.447+13C>T - COL3A1_000915 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.472T>A r.(?) p.(Tyr158Asn) - - - Unknown - likely benign g.189851809T>A - - - COL3A1_000996 - - - rs756125442 CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/+ 6 c.479dup r.? p.(Lys161Glnfs*45) frameshift duplication - Both (homozygous) - pathogenic g.189851816dup - - - COL3A1_000078 - PubMed: Plancke et al., 2009 - rs397509377 Unknown - - - - - RNA RT-PCR, SEQ - - EDS, EDSVASC - PubMed: Plancke et al., 2009 The patient is homozygous for the variant and neither parent shows any symptoms of EDS. The variant is described as being in exon 5, but is in exon 6, using the accepted conventional exon numbering scheme. This patient was subsequently described as Patient 3 by PubMed: Vandervore et al., 2017. - - - - - - - - 1 Raymond Dalgleish
+/+ 6 c.505C>T r.? p.(Leu169Phe) missense substitution Leu2Phe Unknown - pathogenic g.189851842C>T - - - COL3A1_000004 - Anderson et al., 1994 Matrix Biology 14, 392 - - Unknown - - - - - RNA RT-PCR, SEQ - - ? - Anderson et al., 1994 Matrix Biology 14, 392 - - - - - - - - - 1 Raymond Dalgleish
-?/. - c.505C>T r.(?) p.(Leu169Phe) - - - Unknown - likely benign g.189851842C>T - COL3A1(NM_000090.3):c.505C>T (p.L169F) - COL3A1_000004 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.508G>C r.(?) p.(Ala170Pro) - - - Unknown - VUS g.189851845G>C - COL3A1(NM_000090.3):c.508G>C (p.A170P) - COL3A1_000882 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. 5 c.515A>C r.(?) p.(Tyr172Ser) - - - Paternal (inferred) - likely benign g.189851852A>C g.188987126A>C - - COL3A1_000965 - Leone 2023, submitted - - Germline - - - - - DNA SEQ, SEQ-NG blood - EDS P-0142 Leone 2023, submitted - - - Italy - - - - - 1 Maria Pia Leone
+/+? 6i c.528+5G>A r.? - splicing affected? substitution - Unknown - likely pathogenic g.189851870G>A - - - COL3A1_000736 - PubMed: Henneton et al, 2019 - - Unknown - - - - - DNA MLPA, RT-PCR, SEQ - - ? Patient 101 PubMed: Henneton et al, 2019 Patient is a 33 year old female. This patient was subsequently described in PubMed: Frank et al., 2019 as patient 91. - - - - - - - - 1 Raymond Dalgleish
+/. - c.528+5G>A r.spl? p.? - - - Unknown - pathogenic (dominant) g.189851870G>A g.188987144G>A - - COL3A1_000736 - PubMed: Chuan 2022 - - Germline/De novo (untested) - - - - - DNA SEQ, SEQ-NG - WES epilepsy Pat134 PubMed: Chuan 2022 - F - China - - - - - 1 Johan den Dunnen
-?/. - c.528+424T>C r.(=) p.(=) - - - Unknown - likely benign g.189852289T>C - COL3A1(NM_000090.4):c.528+424T>C - COL3A1_000878 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.529-124_529-114del r.(=) p.(=) - - - Unknown - likely benign g.189852683_189852693del g.188987957_188987967del COL3A1(NM_000090.3):c.529-124_529-114delAGTTATCAAAA - COL3A1_000822 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/+ 7 c.530G>A r.? p.(Gly177Asp) missense substitution Gly10Asp Unknown - pathogenic g.189852808G>A - - - COL3A1_000588 - PubMed: Frank et al., 2015 - - Unknown - - - - - DNA SEQ - - EDS, EDSVASC - PubMed: Frank et al., 2015 This patient was subsequently described in PubMed: Legrand et al., 2019. - - - - - - - - 1 Xavier Jeunemaitre
-/- 7 c.531C>A r.? p.(=) silent substitution - Unknown - likely benign g.189852809C>A - - - COL3A1_000183 - PubMed: Chan et al., 2008 - rs41272797 Unknown - - - - - DNA PCR, SEQ - - ? - PubMed: Chan et al., 2008 This is a non-pathogenic variant. - - - - - - - - 1 Raymond Dalgleish
+/+ 7 c.536del r.? p.(Pro179Glnfs*43) frameshift deletion Pro12Glnfs*43 Unknown - pathogenic g.189852814del - - - COL3A1_000742 - PubMed: Weerakkody et al., 2018 - - Unknown - - - - - DNA SEQ-NG, PCRm - - TAAD - PubMed: Weerakkody et al., 2018 The technique used was the custom exome panel. - - - - - - - - 1 Raymond Dalgleish
+/. - c.537_554del r.(?) p.(Pro181_Gly186del) - - - Unknown - pathogenic (dominant) g.189852815_189852832del g.188988089_188988106del - - COL3A1_000966 - - - - Germline/De novo (untested) - - - - - DNA SEQ-NG - blood EDSVASC 117* - relative F - United Kingdom (Great Britain) - - - - - 1 Duncan Baker
+/+ 7 c.539G>A r.? p.(Gly180Asp) missense substitution Gly13Asp Unknown - pathogenic g.189852817G>A - - - COL3A1_000250 - PubMed: Naing et al., 2011 - - Unknown - - - - - DNA SEQ, MCA - - EDS, EDSVASC - PubMed: Naing et al., 2011 - - - Japan Japanese - - - - 1 Raymond Dalgleish
+/+ 7 c.539G>A r.? p.(Gly180Asp) missense substitution Gly13Asp Unknown - pathogenic g.189852817G>A - - - COL3A1_000250 - PubMed: Frank et al., 2015 - - Unknown - - - - - DNA SEQ - - EDS, EDSVASC - PubMed: Frank et al., 2015 This patient was subsequently described as Index Patient 219 (30F) in PubMed: Henneton et al., 2019. This patient was described as Patient 1 in PubMed: Frank et al., 2019 and was also described in PubMed: Legrand et al., 2019. - - - - - - - - 1 Xavier Jeunemaitre
+/+ 7 c.539G>A r.? p.(Gly180Asp) missense substitution Gly13Asp Unknown - pathogenic g.189852817G>A - - - COL3A1_000250 - PubMed: Pepin et al., 2014 - - Unknown - - - - - DNA, RNA PCR, PCR, RT-PCR, SEQ - - EDS, EDSVASC - PubMed: Pepin et al., 2014 - - - - - - - - - 1 Peter Byers
+/. - c.539G>A r.(?) p.(Gly180Asp) - - - Unknown - pathogenic (dominant) g.189852817G>A g.188988091G>A - - COL3A1_000250 - - - - Germline/De novo (untested) - - - - - DNA SEQ-NG - blood EDSVASC 157 - proband M - United Kingdom (Great Britain) - - - - - 2 Duncan Baker
+/+ - c.547G>A r.(?) p.(Gly183Ser) missense - - Parent #1 - pathogenic g.189852825G>A g.188988099G>A - - COL3A1_000006 1 heterozygous, no homozygous; Clinindb (India) PubMed: Narang 2020, Journal: Narang 2020 - rs121912926 Germline - 1/2780 individuals - - - DNA arraySNP - Infinium Global Screening Array v1.0 ? - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - 1 Mohammed Faruq
+/+ 7 c.547G>A r.? p.(Gly183Ser) missense substitution Gly16Ser Unknown - pathogenic g.189852825G>A - - - COL3A1_000006 - PubMed: Pepin et al., 2000 PubMed: Pepin et al., 2014 - - Unknown - - - - - RNA RT-PCR, SEQ, SSCA - - EDS, EDSVASC - PubMed: Pepin et al., 2000 PubMed: Pepin et al., 2014 - - - - - - - - - 1 Peter Byers
+/+ 7 c.547G>A r.? p.(Gly183Ser) missense substitution Gly16Ser Unknown - pathogenic g.189852825G>A - - - COL3A1_000006 - PubMed: Pepin et al., 2000 PubMed: Pepin et al., 2014 - - Unknown - - - - - RNA RT-PCR, SEQ, SSCA - - EDS, EDSVASC - PubMed: Pepin et al., 2000 PubMed: Pepin et al., 2014 - - - - - - - - - 1 Peter Byers
+/+ 7 c.547G>A r.? p.(Gly183Ser) missense substitution Gly16Ser Unknown - pathogenic g.189852825G>A - - - COL3A1_000006 - PubMed: Pepin et al., 2000 PubMed: Pepin et al., 2014 - - Unknown - - - - - RNA RT-PCR, SEQ, SSCA - - EDS, EDSVASC - PubMed: Pepin et al., 2000 PubMed: Pepin et al., 2014 - - - - - - - - - 1 Peter Byers
+/+ 7 c.547G>A r.? p.(Gly183Ser) missense substitution Gly16Ser Unknown - pathogenic g.189852825G>A - - - COL3A1_000006 - PubMed: Pepin et al., 2000 PubMed: Pepin et al., 2014 - - Unknown - - - - - RNA RT-PCR, SEQ, SSCA - - EDS, EDSVASC - PubMed: Pepin et al., 2000 PubMed: Pepin et al., 2014 - - - - - - - - - 1 Peter Byers
+/+ 7 c.547G>A r.? p.(Gly183Ser) missense substitution Gly16Ser Unknown - pathogenic g.189852825G>A - - - COL3A1_000006 - PubMed: Pepin et al., 2000 PubMed: Pepin et al., 2014 - - Unknown - - - - - RNA RT-PCR, SEQ, SSCA - - EDS, EDSVASC - PubMed: Pepin et al., 2000 PubMed: Pepin et al., 2014 - - - - - - - - - 1 Peter Byers
+/+ 7 c.547G>A r.? p.(Gly183Ser) missense substitution Gly16Ser Unknown - pathogenic g.189852825G>A - - - COL3A1_000006 - PubMed: Pepin et al., 2000 PubMed: Pepin et al., 2014 - - Unknown - - - - - RNA RT-PCR, SEQ, SSCA - - EDS, EDSVASC - PubMed: Pepin et al., 2000 PubMed: Pepin et al., 2014 - - - - - - - - - 1 Peter Byers
+/+ 7 c.547G>A r.? p.(Gly183Ser) missense substitution Gly16Ser Unknown - pathogenic g.189852825G>A - - - COL3A1_000006 - PubMed: Pepin et al., 2000 PubMed: Pepin et al., 2014 - - Unknown - - - - - RNA RT-PCR, SEQ, SSCA - - EDS, EDSVASC - PubMed: Pepin et al., 2000 PubMed: Pepin et al., 2014 - - - - - - - - - 1 Peter Byers
?/+ 7 c.547G>A r.? p.(Gly183Ser) missense substitution Gly16Ser Unknown - pathogenic g.189852825G>A - - - COL3A1_000006 - - - - Unknown - - - - - DNA SEQ - - EDS, EDSVASC P002 - - - - - white - - - - 1 Javier Garcia-Planells
+/+ 7 c.547G>A r.? p.(Gly183Ser) missense substitution Gly16Ser Unknown - pathogenic g.189852825G>A - - - COL3A1_000006 - PubMed: Mortani Barbosa et al., 2011 - - Unknown - - - - - ? ? - - EDS, EDSVASC Patient 2 PubMed: Mortani Barbosa et al., 2011 The protein level variant description is incorrectly described as p.G16S. - - - - - - - - 1 Raymond Dalgleish
+/+ 7 c.547G>A r.? p.(Gly183Ser) missense substitution Gly16Ser Unknown - pathogenic g.189852825G>A - - - COL3A1_000006 - PubMed: Frank et al., 2015 - - Unknown - - - - - DNA SEQ - - EDS, EDSVASC - PubMed: Frank et al., 2015 This patient was subsequently described in PubMed: Legrand et al., 2019. - - - - - - - - 1 Xavier Jeunemaitre
+/+ 7 c.547G>A r.? p.(Gly183Ser) missense substitution Gly16Ser Unknown - pathogenic g.189852825G>A - - - COL3A1_000006 - PubMed: Kerwin et al., 2008 PubMed: Pepin et al., 2014 - - Unknown - - - - - DNA, RNA PCR, RT-PCR, SEQ - - EDS, EDSVASC - PubMed: Kerwin et al., 2008 PubMed: Pepin et al., 2014 This patient was identified as Subject 00-1123 by PubMed: Kerwin et al., 2008. - - - - - - - - 1 Peter Byers
+/+ 7 c.547G>A r.? p.(Gly183Ser) missense substitution Gly16Ser Unknown - pathogenic g.189852825G>A - - - COL3A1_000006 - PubMed: Pepin et al., 2014 - - Unknown - - - - - DNA SEQ - - EDS, EDSVASC - PubMed: Pepin et al., 2014 de novo - - - - - - - - 1 Peter Byers
+/+ 7 c.547G>A r.? p.(Gly183Ser) missense substitution Gly16Ser Maternal (inferred) - pathogenic g.189852825G>A - - - COL3A1_000006 - PubMed: Pepin et al., 2014 - - Unknown - - - - - DNA SEQ - - EDS, EDSVASC - PubMed: Pepin et al., 2014 - - - - - - - - - 1 Peter Byers
+/+ 7 c.547G>A r.? p.(Gly183Ser) missense substitution Gly16Ser Paternal (inferred) - pathogenic g.189852825G>A - - - COL3A1_000006 - PubMed: Pepin et al., 2014 - - Unknown - - - - - DNA, RNA PCR, PCR, RT-PCR, SEQ - - EDS, EDSVASC - PubMed: Pepin et al., 2014 - - - - - - - - - 1 Peter Byers
+/+ 7 c.547G>A r.? p.(Gly183Ser) missense substitution Gly16Ser Unknown - pathogenic g.189852825G>A - - - COL3A1_000006 - PubMed: Pepin et al., 2014 - - Unknown - - - - - DNA, RNA PCR, RT-PCR, SEQ - - EDS, EDSVASC - PubMed: Pepin et al., 2014 de novo - - - - - - - - 1 Peter Byers
+/+ 7 c.547G>A r.? p.(Gly183Ser) missense substitution Gly16Ser Unknown - pathogenic g.189852825G>A - - - COL3A1_000006 - PubMed: Pepin et al., 2014 - - Unknown - - - - - DNA, RNA PCR, RT-PCR, SEQ - - EDS, EDSVASC - PubMed: Pepin et al., 2014 de novo - - - - - - - - 1 Peter Byers
+/+ 7 c.547G>A r.? p.(Gly183Ser) missense substitution Gly16Ser Unknown - pathogenic g.189852825G>A - - - COL3A1_000006 - PubMed: Pepin et al., 2014 - - Unknown - - - - - DNA SEQ - - EDS, EDSVASC - PubMed: Pepin et al., 2014 de novo - - - - - - - - 1 Peter Byers
+/+ 7 c.547G>A r.? p.(Gly183Ser) missense substitution Gly16Ser Unknown - pathogenic g.189852825G>A - - - COL3A1_000006 - PubMed: Pepin et al., 2014 - - Unknown - - - - - DNA, RNA PCR, RT-PCR, SEQ - - EDS, EDSVASC - PubMed: Pepin et al., 2014 - - - - - - - - - 1 Peter Byers
+/+ 7 c.547G>A r.? p.(Gly183Ser) missense substitution Gly16Ser Unknown - pathogenic g.189852825G>A - - - COL3A1_000006 - PubMed: Pepin et al., 2014 - - Unknown - - - - - DNA, RNA PCR, RT-PCR, SEQ - - EDS, EDSVASC - PubMed: Pepin et al., 2014 affected sib - - - - - - - - 1 Peter Byers
+/+ 7 c.547G>A r.? p.(Gly183Ser) missense substitution Gly16Ser Unknown - pathogenic g.189852825G>A - - - COL3A1_000006 - PubMed: Pepin et al., 2014 - - Unknown - - - - - DNA SEQ - - EDS, EDSVASC - PubMed: Pepin et al., 2014 - - - - - - - - - 1 Peter Byers
+/+ 7 c.547G>A r.? p.(Gly183Ser) missense substitution Gly16Ser Unknown - pathogenic g.189852825G>A - - - COL3A1_000006 - PubMed: Pepin et al., 2014 - - Unknown - - - - - DNA, RNA PCR, RT-PCR, SEQ - - EDS, EDSVASC - PubMed: Pepin et al., 2014 - - - - - - - - - 1 Peter Byers
+/+ 7 c.547G>A r.? p.(Gly183Ser) missense substitution Gly16Ser Unknown - pathogenic g.189852825G>A - - - COL3A1_000006 - - - - Unknown - - - - - DNA SEQ - - EDS, EDSVASC - - This patient was subsequently described in PubMed: Legrand et al., 2019. - - - - - - - - 1 Xavier Jeunemaitre
+/+ 7 c.547G>A r.(?) p.(Gly183Ser) missense substitution Gly16Ser Unknown ACMG pathogenic g.189852825G>A g.188988099G>A - - COL3A1_000006 - PubMed: Yamaguchi et al., 2022 - - Germline ? - - - - DNA SEQ-NG peripheral blood - EDSVASC 1 PubMed: Yamaguchi et al., 2022 - F ? - - - - - - 1 Oumaima Nehaili
+/+ 7 c.547G>A r.(?) p.(Gly183Ser) missense substitution Gly16Ser Unknown ACMG pathogenic g.189852825G>A g.188988099G>A - - COL3A1_000006 - PubMed: Yamaguchi et al., 2022 - - Germline - - - - - DNA SEQ-NG peripheral blood - EDSVASC 2 PubMed: Yamaguchi et al., 2022 - F ? - - - - - - 1 Oumaima Nehaili
+/. - c.547G>A r.(?) p.(Gly183Ser) - - - Unknown - pathogenic (dominant) g.189852825G>A g.188988099G>A - - COL3A1_000006 - - - - Germline/De novo (untested) - - - - - DNA SEQ-NG - blood EDSVASC 76* - Proband F - United Kingdom (Great Britain) - - - - - 1 Duncan Baker
+/+ - c.547G>A r.(?) p.(Gly183Ser) missense substitution - Unknown - likely pathogenic (dominant) g.189852825G>A - - - COL3A1_000006 - - - - Not applicable - - - - - DNA SEQ-NG-I - - EDSVASC - - - - - - - - - - - 1 Lucia Micale
+/+ 7 c.547G>C r.? p.(Gly183Arg) missense substitution Gly16Arg Unknown - pathogenic g.189852825G>C - - - COL3A1_000374 - PubMed: Pepin et al., 2014 - - Unknown - - - - - DNA, RNA PCR, RT-PCR, SEQ - - EDS, EDSVASC - PubMed: Pepin et al., 2014 - - - - - - - - - 1 Peter Byers
+/+ 7 c.547G>T r.? p.(Gly183Cys) missense substitution Gly16Cys Unknown - pathogenic g.189852825G>T - - - COL3A1_000005 - PubMed: Smith et al., 1997 PubMed: Pepin et al., 2014 - - Unknown - - - - - RNA RT-PCR, SEQ, SSCA - - EDS, EDSVASC - PubMed: Smith et al., 1997 PubMed: Pepin et al., 2014 This patient was identified as Sample 1 by PubMed: Smith et al., 1997 and was subsequently described by PubMed: Pepin et al., 2000. - - - - - - - - 1 Peter Byers
+/. - c.548G>A r.(?) p.(Gly183Asp) - - - Unknown - pathogenic g.189852826G>A g.188988100G>A COL3A1(NM_000090.4):c.548G>A (p.G183D) - COL3A1_000001 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/+ 7 c.548G>A r.? p.(Gly183Asp) missense substitution Gly16Asp Unknown - pathogenic g.189852826G>A - - - COL3A1_000001 - PubMed: Pepin et al., 2000 PubMed: Pepin et al., 2014 - - Unknown - - - - - RNA RT-PCR, SEQ, SSCA - - EDS, EDSVASC - PubMed: Pepin et al., 2000 PubMed: Pepin et al., 2014 - - - - - - - - - 1 Peter Byers
+/+ 7 c.548G>A r.? p.(Gly183Asp) missense substitution Gly16Asp Unknown - pathogenic g.189852826G>A - - - COL3A1_000001 - PubMed: Frank et al., 2015 - - Unknown - - - - - DNA SEQ - - EDS, EDSVASC - PubMed: Frank et al., 2015 This patient was subsequently as Index Patient 111 (37F) in PubMed: Henneton et al., 2019. This patient was described as Patient 2 in PubMed: Frank et al., 2019 and was subsequently described in PubMed: Legrand et al., 2019. - - - - - - - - 1 Xavier Jeunemaitre
+?/+ - c.548G>A r.? p.(Gly183Asp) missense substitution - Unknown - pathogenic g.189852826G>A - - - COL3A1_000001 - - - - Germline/De novo (untested) - - - - - DNA SEQ-NG - - EDSVASC - - - - - - - - - - - 1 Niamh Wilkinson
+/+ 7 c.548G>C r.? p.(Gly183Ala) missense substitution Gly16Ala Unknown - pathogenic g.189852826G>C - - - COL3A1_000297 - PubMed: Morissette et al., 2014 - - Unknown - - - - - DNA IHC, SEQ, Western - - EDS, EDSVASC - PubMed: Morissette et al., 2014 Patient 17, Male, 51y, arterial event. His daughter, patient 18, AN_002818, female, 21y, arterial event, carries the same mutation - - - - - - - - 1 Zhi Xu
+/+ 7 c.548G>C r.? p.(Gly183Ala) missense substitution Gly16Ala Paternal (confirmed) - pathogenic g.189852826G>C - - - COL3A1_000297 - PubMed: Pepin et al., 2014 - - Unknown - - - - - DNA, RNA PCR, RT-PCR, SEQ - - EDS, EDSVASC - PubMed: Pepin et al., 2014 mosaic parent - - - - - - - - 1 Peter Byers
+/. - c.548G>T r.(?) p.(Gly183Val) - - - Unknown - pathogenic g.189852826G>T g.188988100G>T COL3A1(NM_000090.3):c.548G>T (p.G183V) - COL3A1_000823 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
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