Full data view for gene B4GALT7

Ehlers Danlos Syndrome Variant Database


Information The variants shown are described using the NM_007255.2 transcript reference sequence.

94 entries on 1 page. Showing entries 1 - 94.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Predicted     

Type/DNA     

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     
?/. - c.-4899C>T r.(?) p.(=) - - Unknown - VUS g.177022313C>T - TMED9(NM_017510.4):c.604C>T (p.(Arg202Trp)) - B4GALT7_000050 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.50+12_50+14dup r.(=) p.(=) - - Unknown - VUS g.177027273_177027275dup g.177600272_177600274dup B4GALT7(NM_007255.2):c.50+4_50+5insGCG (p.?) - B4GALT7_000037 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.51-11G>A r.(=) p.(=) - - Unknown - likely benign g.177031169G>A g.177604168G>A B4GALT7(NM_007255.3):c.51-11G>A - B4GALT7_000038 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. 02 c.122T>C r.(?) p.(Leu41Pro) missense substitution Paternal (confirmed) - pathogenic (recessive) g.177031251T>C g.177604250T>C - - B4GALT7_000004 - PubMed: Guo 2013 - - Germline - - - - - DNA SEQ, SEQ-NG - WES EDS patient PubMed: Guo 2013, PubMed: Guo 2014 2-generation family, 1 affected, unaffected heterozygous carrier parents M no United States - - - - - 1 Johan den Dunnen
-/. - c.219T>C r.(?) p.(Arg73=) - - Unknown - benign g.177031348T>C g.177604347T>C B4GALT7(NM_007255.3):c.219T>C (p.R73=) - B4GALT7_000039 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-/. - c.219T>C r.(?) p.(Arg73=) - - Unknown - benign g.177031348T>C g.177604347T>C B4GALT7(NM_007255.3):c.219T>C (p.R73=) - B4GALT7_000039 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.256G>C r.(?) p.(Glu86Gln) - - Unknown - VUS g.177031385G>C - B4GALT7(NM_007255.2):c.256G>C (p.(Glu86Gln)) - B4GALT7_000049 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.277C>T r.(?) p.(His93Tyr) - - Unknown - likely benign g.177031406C>T g.177604405C>T B4GALT7(NM_007255.2):c.277C>T (p.H93Y, p.(His93Tyr)), B4GALT7(NM_007255.3):c.277C>T (p.H93Y) - B4GALT7_000030 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.277C>T r.(?) p.(His93Tyr) - - Unknown - likely benign g.177031406C>T - B4GALT7(NM_007255.2):c.277C>T (p.H93Y, p.(His93Tyr)), B4GALT7(NM_007255.3):c.277C>T (p.H93Y) - B4GALT7_000030 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.277C>T r.(?) p.(His93Tyr) - - Unknown - VUS g.177031406C>T - B4GALT7(NM_007255.2):c.277C>T (p.H93Y, p.(His93Tyr)), B4GALT7(NM_007255.3):c.277C>T (p.H93Y) - B4GALT7_000030 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
./. - c.277dup r.(?) p.(His93Profs*73) - - Paternal (confirmed) - pathogenic g.177031406dup g.177604405dup - - B4GALT7_000036 - PubMed: DDDS 2015, Journal: DDDS 2015 - - Germline - - - - - DNA SEQ, SEQ-NG-I - - ? - PubMed: DDDS 2015, Journal: DDDS 2015 family, 1 affected M - United Kingdom (Great Britain) - - - Decipher - 1 Johan den Dunnen
+/+ 02 c.277dup r.(?) p.(His93Profs*73) frameshift duplication Maternal (confirmed) - pathogenic (recessive) g.177031406dup g.177604405dup 277dupC - B4GALT7_000005 - PubMed: Caraffi 2019 - - Germline - - - - - DNA SEQ - - EDS Pat1 PubMed: Caraffi 2019 2-generation family, 1 affected, unaffected heterozygous carrier parents M no Italy - - - - - 1 Johan den Dunnen
+/. 02 c.277dup r.(?) p.(His93Profs*73) frameshift duplication Paternal (confirmed) - pathogenic (recessive) g.177031406dup g.177604405dup 277dupC - B4GALT7_000005 - PubMed: Salter 2016 - - Germline - - - - - DNA SEQ, SEQ-NG - WES trio EDS Pat1 PubMed: Salter 2016 - M - United Kingdom (Great Britain) - - - - - 1 Johan den Dunnen
?/. - c.277dup r.(?) p.(His93Profs*73) - - Unknown - VUS g.177031406dup - B4GALT7(NM_007255.2):c.277dup (p.(His93Profs*73)), B4GALT7(NM_007255.3):c.277dupC (p.H93Pfs*73) - B4GALT7_000005 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.277dup r.(?) p.(His93Profs*73) - - Unknown - pathogenic g.177031406dup - B4GALT7(NM_007255.2):c.277dup (p.(His93Profs*73)), B4GALT7(NM_007255.3):c.277dupC (p.H93Pfs*73) - B4GALT7_000005 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.278A>G r.(?) p.(His93Arg) - - Unknown - VUS g.177031407A>G - B4GALT7(NM_007255.2):c.278A>G (p.(His93Arg)) - B4GALT7_000053 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-/. - c.297G>T r.(?) p.(Val99=) - - Unknown - benign g.177031426G>T - B4GALT7(NM_007255.3):c.297G>T (p.V99=) - B4GALT7_000045 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.315C>T r.(?) p.(=) - - Unknown - likely benign g.177031444C>T - B4GALT7(NM_007255.3):c.315C>T (p.F105=) - B4GALT7_000052 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+?/- 2 c.319G>C r.(?) p.(Glu107Gln) missense substitution Paternal (confirmed) - VUS g.177031448G>C - - - B4GALT7_000012 - PubMed: Wang et al., 2020 - - Unknown - - - - - DNA SEQ-NG - - ? - PubMed: Wang et al., 2020 The variants were detected by medical exome sequencing of 95 patients with clinical manifestations of intellectual disability.The technique used was the custom NGS Gene panel. The technique used was whole genome sequencing. - - - - - - - - 1 Raymond Dalgleish
+/+? 02 c.398A>G r.(?) p.(Gln133Arg) missense substitution Paternal (confirmed) - pathogenic (recessive) g.177031527A>G g.177604526A>G - - B4GALT7_000028 - PubMed: Mihalic Mosher 2019 - rs1370937766 Germline - - - - - DNA SEQ, SEQ-NG - WES trio EDS patient PubMed: Mihalic Mosher 2019 2-generation family, 3 affected pregnancies, unaffected heterozygous carrier parents - - United States - - - - - 1 Johan den Dunnen
-?/. - c.411C>T r.(?) p.(Phe137=) - - Unknown - likely benign g.177031540C>T g.177604539C>T B4GALT7(NM_007255.2):c.411C>T (p.F137=, p.(Phe137=)), B4GALT7(NM_007255.3):c.411C>T (p.F137=) - B4GALT7_000011 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.411C>T r.(?) p.(Phe137=) - - Unknown - likely benign g.177031540C>T g.177604539C>T B4GALT7(NM_007255.2):c.411C>T (p.F137=, p.(Phe137=)), B4GALT7(NM_007255.3):c.411C>T (p.F137=) - B4GALT7_000011 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.411C>T r.(?) p.(Phe137=) - - Unknown - likely benign g.177031540C>T g.177604539C>T B4GALT7(NM_007255.2):c.411C>T (p.F137=, p.(Phe137=)), B4GALT7(NM_007255.3):c.411C>T (p.F137=) - B4GALT7_000011 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.413+6G>A r.(=) p.(=) - - Unknown - likely benign g.177031548G>A - B4GALT7(NM_007255.2):c.413+6G>A (p.(=)) - B4GALT7_000040 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-/. - c.413+12C>G r.(=) p.(=) - - Unknown - benign g.177031554C>G - B4GALT7(NM_007255.3):c.413+12C>G - B4GALT7_000042 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-/. - c.413+508C>G r.(=) p.(=) - - Unknown - benign g.177032050C>G g.177605049C>G B4GALT7(NM_007255.3):c.413+508C>G - B4GALT7_000032 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-/. - c.414-20G>A r.(=) p.(=) - - Unknown - benign g.177034283G>A g.177607282G>A B4GALT7(NM_007255.3):c.414-20G>A - B4GALT7_000033 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
./. - c.421C>T r.(?) p.(Arg141Trp) - - Paternal (confirmed) - pathogenic g.177034310C>T g.177607309C>T - - B4GALT7_000008 - PubMed: DDDS 2015, Journal: DDDS 2015 - - Germline - - - - - DNA SEQ, SEQ-NG-I - - ? - PubMed: DDDS 2015, Journal: DDDS 2015 family, 1 affected F - United Kingdom (Great Britain) - - - Decipher - 1 Johan den Dunnen
+/+? 03 c.421C>T r.(?) p.(Arg141Trp) missense substitution Paternal (confirmed) - pathogenic (recessive) g.177034310C>T g.177607309C>T - - B4GALT7_000008 - PubMed: Salter 2016 - - Germline - - - - - DNA SEQ, SEQ-NG - WES trio EDS Pat2 PubMed: Salter 2016 - F - United Kingdom (Great Britain) - - - - - 1 Johan den Dunnen
+/+? 3 c.421C>T r.(?) p.(Arg141Trp) missense substitution Maternal (confirmed) - likely pathogenic g.177034310C>T - - - B4GALT7_000010 - PubMed: Sandler-Wilson et al., 2019 - - Unknown - - - - - DNA SEQ, SEQ-NG - - EDS, EDSSPD1 - PubMed: Sandler-Wilson et al., 2019 The patient had a female sibling who also carried both variants and was diagnosed with spEDS. The technique used was whole exome sequencing. - - - Partly French - - - - 1 Raymond Dalgleish
?/. - c.421C>T r.(?) p.(Arg141Trp) - - Unknown - VUS g.177034310C>T - B4GALT7(NM_007255.3):c.421C>T (p.(Arg141Trp)) - B4GALT7_000008 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.517C>T r.(?) p.(=) - - Unknown - likely benign g.177034406C>T - B4GALT7(NM_007255.3):c.517C>T (p.L173=) - B4GALT7_000051 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. 03 c.557C>A r.557c>a p.Ala186Asp missense substitution Maternal (confirmed) - pathogenic (recessive) g.177034446C>A g.177607445C>A 186G>T - B4GALT7_000001 - PubMed: Okajima 1999, PubMed: Almeida 1999 - - Germline - - - - - DNA, RNA RT-PCR, SEQ - - EDS patient PubMed: Okajima 1999, PubMed: Almeida 1999, PubMed: Kresse 1987, PubMed: Quentin 1990, PubMed: Furukawa 2002, PubMed: Gotte 2005 2-generation family, 1 affected, unaffected heterozygous carrier parents/relatives M - Denmark - - - - - 1 Johan den Dunnen
?/. - c.604G>C r.(?) p.(Gly202Arg) - - Unknown - VUS g.177034493G>C g.177607492G>C B4GALT7(NM_007255.2):c.604G>C (p.(Gly202Arg)) - B4GALT7_000022 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-/- 3 c.614T>C r.(?) p.(Leu205Pro) missense substitution Maternal (confirmed) - likely benign g.177034503T>C - - - B4GALT7_000013 - PubMed: Wang et al., 2020 - - Unknown - - - - - DNA SEQ-NG - - ? - PubMed: Wang et al., 2020 The variants were detected by medical exome sequencing of 95 patients with clinical manifestations of intellectual disability.The technique used was the custom NGS Gene panel. The technique used was whole genome sequencing. - - - - - - - - 1 Raymond Dalgleish
+/. 03 c.617T>C r.617c>u p.Leu206Pro missense substitution Paternal (confirmed) - pathogenic (recessive) g.177034506T>C g.177607505T>C 206A>C - B4GALT7_000002 - PubMed: Okajima 1999, PubMed: Almeida 1999 - - Germline - - - - - DNA, RNA RT-PCR, SEQ - - EDS patient PubMed: Okajima 1999, PubMed: Almeida 1999, PubMed: Kresse 1987, PubMed: Quentin 1990, PubMed: Furukawa 2002, PubMed: Gotte 2005 2-generation family, 1 affected, unaffected heterozygous carrier parents/relatives M - Denmark - - - - - 1 Johan den Dunnen
+/. - c.617T>C r.(?) p.(Leu206Pro) - - Unknown - pathogenic g.177034506T>C - B4GALT7(NM_007255.3):c.617T>C (p.(Leu206Pro)) - B4GALT7_000002 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/+? 03 c.628C>T r.(?) p.(His210Tyr) missense substitution Paternal (confirmed) - pathogenic (recessive) g.177034517C>T g.177607516C>T - - B4GALT7_000006 - PubMed: Caraffi 2019 - - Germline - - - - - DNA SEQ - - EDS Pat1 PubMed: Caraffi 2019 2-generation family, 1 affected, unaffected heterozygous carrier parents M no Italy - - - - - 1 Johan den Dunnen
-?/. - c.634C>T r.(?) p.(Arg212Trp) - - Unknown - likely benign g.177034523C>T - B4GALT7(NM_007255.2):c.634C>T (p.(Arg212Trp)) - B4GALT7_000041 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.639G>A r.(?) p.(=) - - Unknown - VUS g.177034528G>A - B4GALT7(NM_007255.3):c.639G>A (p.(Leu213=)) - B4GALT7_000054 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+?/. - c.639+5G>A r.spl? p.? - - Unknown - likely pathogenic g.177034533G>A g.177607532G>A B4GALT7(NM_007255.3):c.639+5G>A - B4GALT7_000014 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.640-93G>A r.(=) p.(=) - - Unknown - likely benign g.177035447G>A - B4GALT7(NM_007255.3):c.640-93G>A - B4GALT7_000046 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.640-42C>A r.(=) p.(=) - - Unknown - likely benign g.177035498C>A - B4GALT7(NM_007255.3):c.640-42C>A - B4GALT7_000047 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.641G>A r.(?) p.(Cys214Tyr) - - Maternal (confirmed) - pathogenic (recessive) g.177035541G>A g.177608540G>A - - B4GALT7_000007 - PubMed: DDDS 2015, Journal: DDDS 2015 - - Germline - - - - - DNA SEQ, SEQ-NG-I - - ? - PubMed: DDDS 2015, Journal: DDDS 2015 family, 1 affected M - United Kingdom (Great Britain) - - - Decipher - 1 Johan den Dunnen
+/. 04 c.641G>A r.(?) p.(Cys214Tyr) missense substitution Maternal (confirmed) - pathogenic (recessive) g.177035541G>A g.177608540G>A - - B4GALT7_000007 - PubMed: Salter 2016 - - Germline - - - - - DNA SEQ, SEQ-NG - WES trio EDS Pat1 PubMed: Salter 2016 - M - United Kingdom (Great Britain) - - - - - 1 Johan den Dunnen
+?/. - c.681G>T r.(?) p.(Glu227Asp) - - Unknown - likely pathogenic g.177035581G>T g.177608580G>T B4GALT7(NM_007255.3):c.681G>T (p.E227D) - B4GALT7_000015 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.698G>A r.(?) p.(Arg233Gln) - - Unknown - likely benign g.177035598G>A g.177608597G>A B4GALT7(NM_007255.2):c.698G>A (p.R233Q) - B4GALT7_000016 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.700C>T r.(?) p.(Arg234Cys) - - Unknown - VUS g.177035600C>T g.177608599C>T B4GALT7(NM_007255.2):c.700C>T (p.R234C) - B4GALT7_000017 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.723+1G>A r.spl? p.? - - Unknown - VUS g.177035624G>A - B4GALT7(NM_007255.2):c.723+1G>A (p.?) - B4GALT7_000043 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.723+19C>T r.(=) p.(=) - - Unknown - likely benign g.177035642C>T g.177608641C>T B4GALT7(NM_007255.3):c.723+19C>T - B4GALT7_000023 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.723+20G>A r.(=) p.(=) - - Unknown - likely benign g.177035643G>A g.177608642G>A B4GALT7(NM_007255.3):c.723+20G>A - B4GALT7_000018 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.731G>A r.(?) p.(Arg244His) - - Unknown - VUS g.177035918G>A - B4GALT7(NM_007255.2):c.731G>A (p.(Arg244His)) - B4GALT7_000048 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-/. - c.777T>C r.(?) p.(His259=) - - Unknown - benign g.177035964T>C g.177608963T>C B4GALT7(NM_007255.3):c.777T>C (p.H259=) - B4GALT7_000024 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-/. - c.777T>C r.(?) p.(His259=) - - Unknown - benign g.177035964T>C g.177608963T>C B4GALT7(NM_007255.3):c.777T>C (p.H259=) - B4GALT7_000024 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.793A>G r.(?) p.(Lys265Glu) - - Unknown - VUS g.177035980A>G g.177608979A>G B4GALT7(NM_007255.2):c.793A>G (p.(Lys265Glu)) - B4GALT7_000025 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/? 5 c.808C>T r.(?) p.(Arg270Cys) - - Both (homozygous) - pathogenic g.177035995C>T g.177608994C>T - - B4GALT7_000003 - - - rs28937869 Germline - - - - - DNA SEQ, SEQ-NG-S blood - EDS Pat22 PubMed: Cartault 2015, Journal: Cartault 2015 large multi-generation family, 22 afecteds, unaffected heterozygote carriers F - Reunion white - - - - 22 Francois Cartault
./. - c.808C>T r.(?) p.(Arg270Cys) - - Maternal (confirmed) - pathogenic g.177035995C>T g.177608994C>T - - B4GALT7_000003 - PubMed: DDDS 2015, Journal: DDDS 2015 - - Germline - - - - - DNA SEQ, SEQ-NG-I - - ? - PubMed: DDDS 2015, Journal: DDDS 2015 family, 1 affected F - United Kingdom (Great Britain) - - - Decipher - 1 Johan den Dunnen
+/. 05 c.808C>T r.(?) p.(Arg270Cys) missense substitution Both (homozygous) - pathogenic (recessive) g.177035995C>T g.177608994C>T - - B4GALT7_000003 - PubMed: Faiyaz-Ul-Haque 2004 - rs28937869 Germline yes - - - - DNA SEQ - - EDS family PubMed: Faiyaz-Ul-Haque 2004 PubMed: Walker 2004 PubMed: Seidler 2006 4-generation family, 2 affected (F, M), unaffected heterozygous carrier parents/relatives - yes Qatar Arab - - - - 2 Johan den Dunnen
+/. 05 c.808C>T r.(?) p.(Arg270Cys) missense substitution Maternal (confirmed) - pathogenic (recessive) g.177035995C>T g.177608994C>T - - B4GALT7_000003 - PubMed: Guo 2013 PubMed: Guo 2014 - - Germline - - - - - DNA SEQ, SEQ-NG - WES EDS patient PubMed: Guo 2013, PubMed: Guo 2014 2-generation family, 1 affected, unaffected heterozygous carrier parents M no United States - - - - - 1 Johan den Dunnen
+/. 5 c.808C>T r.(?) p.(Arg270Cys) - - Both (homozygous) - pathogenic (recessive) g.177035995C>T g.177608994C>T - - B4GALT7_000003 - PubMed: Cartault 2015, Journal: Cartault 2015 - rs28937869 Germline - - - - - DNA SEQ - - EDS Pat1 PubMed: Cartault 2015, Journal: Cartault 2015 - M - Reunion - - - - - 1 Francois Cartault
+/. 5 c.808C>T r.(?) p.(Arg270Cys) - - Both (homozygous) - pathogenic (recessive) g.177035995C>T g.177608994C>T - - B4GALT7_000003 - PubMed: Cartault 2015, Journal: Cartault 2015 - rs28937869 Germline - - - - - DNA SEQ - - EDS Pat2 PubMed: Cartault 2015, Journal: Cartault 2015 - M - Reunion - - - - - 1 Francois Cartault
+/. 5 c.808C>T r.(?) p.(Arg270Cys) - - Both (homozygous) - pathogenic (recessive) g.177035995C>T g.177608994C>T - - B4GALT7_000003 - PubMed: Cartault 2015, Journal: Cartault 2015 - rs28937869 Germline - - - - - DNA SEQ - - EDS Pat3 PubMed: Cartault 2015, Journal: Cartault 2015 - M - Reunion - - - - - 1 Francois Cartault
+/. 5 c.808C>T r.(?) p.(Arg270Cys) - - Both (homozygous) - pathogenic (recessive) g.177035995C>T g.177608994C>T - - B4GALT7_000003 - PubMed: Cartault 2015, Journal: Cartault 2015 - rs28937869 Germline - - - - - DNA SEQ - - EDS Pat4 PubMed: Cartault 2015, Journal: Cartault 2015 - F - Reunion - - - - - 1 Francois Cartault
+/. 5 c.808C>T r.(?) p.(Arg270Cys) - - Both (homozygous) - pathogenic (recessive) g.177035995C>T g.177608994C>T - - B4GALT7_000003 - PubMed: Cartault 2015, Journal: Cartault 2015 - rs28937869 Germline - - - - - DNA SEQ - - EDS Pat5 PubMed: Cartault 2015, Journal: Cartault 2015 - M - Reunion - - - - - 1 Francois Cartault
+/. 5 c.808C>T r.(?) p.(Arg270Cys) - - Both (homozygous) - pathogenic (recessive) g.177035995C>T g.177608994C>T - - B4GALT7_000003 - PubMed: Cartault 2015, Journal: Cartault 2015 - rs28937869 Germline - - - - - DNA SEQ - - EDS Pat6 PubMed: Cartault 2015, Journal: Cartault 2015 - F - Reunion - - - - - 1 Francois Cartault
+/. 5 c.808C>T r.(?) p.(Arg270Cys) - - Both (homozygous) - pathogenic (recessive) g.177035995C>T g.177608994C>T - - B4GALT7_000003 - PubMed: Cartault 2015, Journal: Cartault 2015 - rs28937869 Germline - - - - - DNA SEQ - - EDS Pat7 PubMed: Cartault 2015, Journal: Cartault 2015 - M - Reunion - - - - - 1 Francois Cartault
+/. 5 c.808C>T r.(?) p.(Arg270Cys) - - Both (homozygous) - pathogenic (recessive) g.177035995C>T g.177608994C>T - - B4GALT7_000003 - PubMed: Cartault 2015, Journal: Cartault 2015 - rs28937869 Germline - - - - - DNA SEQ - - EDS Pat8 PubMed: Cartault 2015, Journal: Cartault 2015 - F - Reunion - - - - - 1 Francois Cartault
+/. 5 c.808C>T r.(?) p.(Arg270Cys) - - Both (homozygous) - pathogenic (recessive) g.177035995C>T g.177608994C>T - - B4GALT7_000003 - PubMed: Cartault 2015, Journal: Cartault 2015 - rs28937869 Germline - - - - - DNA SEQ - - EDS Pat9 PubMed: Cartault 2015, Journal: Cartault 2015 - M - Reunion - - - - - 1 Francois Cartault
+/. 5 c.808C>T r.(?) p.(Arg270Cys) - - Both (homozygous) - pathogenic (recessive) g.177035995C>T g.177608994C>T - - B4GALT7_000003 - PubMed: Cartault 2015, Journal: Cartault 2015 - rs28937869 Germline - - - - - DNA SEQ - - EDS Pat10 PubMed: Cartault 2015, Journal: Cartault 2015 - M - Reunion - - - - - 1 Francois Cartault
+/. 5 c.808C>T r.(?) p.(Arg270Cys) - - Both (homozygous) - pathogenic (recessive) g.177035995C>T g.177608994C>T - - B4GALT7_000003 - PubMed: Cartault 2015, Journal: Cartault 2015 - rs28937869 Germline - - - - - DNA SEQ - - EDS Pat11 PubMed: Cartault 2015, Journal: Cartault 2015 - F - Reunion - - - - - 1 Francois Cartault
+/. 5 c.808C>T r.(?) p.(Arg270Cys) - - Both (homozygous) - pathogenic (recessive) g.177035995C>T g.177608994C>T - - B4GALT7_000003 - PubMed: Cartault 2015, Journal: Cartault 2015 - rs28937869 Germline - - - - - DNA SEQ - - EDS Pat12 PubMed: Cartault 2015, Journal: Cartault 2015 - F - Reunion - - - - - 1 Francois Cartault
+/. 5 c.808C>T r.(?) p.(Arg270Cys) - - Both (homozygous) - pathogenic (recessive) g.177035995C>T g.177608994C>T - - B4GALT7_000003 - PubMed: Cartault 2015, Journal: Cartault 2015 - rs28937869 Germline - - - - - DNA SEQ - - EDS Pat13 PubMed: Cartault 2015, Journal: Cartault 2015 - M - Reunion - - - - - 1 Francois Cartault
+/. 5 c.808C>T r.(?) p.(Arg270Cys) - - Both (homozygous) - pathogenic (recessive) g.177035995C>T g.177608994C>T - - B4GALT7_000003 - PubMed: Cartault 2015, Journal: Cartault 2015 - rs28937869 Germline - - - - - DNA SEQ - - EDS Pat14 PubMed: Cartault 2015, Journal: Cartault 2015 - M - Reunion - - - - - 1 Francois Cartault
+/. 5 c.808C>T r.(?) p.(Arg270Cys) - - Both (homozygous) - pathogenic (recessive) g.177035995C>T g.177608994C>T - - B4GALT7_000003 - PubMed: Cartault 2015, Journal: Cartault 2015 - rs28937869 Germline - - - - - DNA SEQ - - EDS Pat15 PubMed: Cartault 2015, Journal: Cartault 2015 - F - Reunion - - - - - 1 Francois Cartault
+/. 5 c.808C>T r.(?) p.(Arg270Cys) - - Both (homozygous) - pathogenic (recessive) g.177035995C>T g.177608994C>T - - B4GALT7_000003 - PubMed: Cartault 2015, Journal: Cartault 2015 - rs28937869 Germline - - - - - DNA SEQ - - EDS Pat16 PubMed: Cartault 2015, Journal: Cartault 2015 - F - Reunion - - - - - 1 Francois Cartault
+/. 5 c.808C>T r.(?) p.(Arg270Cys) - - Both (homozygous) - pathogenic (recessive) g.177035995C>T g.177608994C>T - - B4GALT7_000003 - PubMed: Cartault 2015, Journal: Cartault 2015 - rs28937869 Germline - - - - - DNA SEQ - - EDS Pat17 PubMed: Cartault 2015, Journal: Cartault 2015 - F - Reunion - - - - - 1 Francois Cartault
+/. 5 c.808C>T r.(?) p.(Arg270Cys) - - Both (homozygous) - pathogenic (recessive) g.177035995C>T g.177608994C>T - - B4GALT7_000003 - PubMed: Cartault 2015, Journal: Cartault 2015 - rs28937869 Germline - - - - - DNA SEQ - - EDS Pat18 PubMed: Cartault 2015, Journal: Cartault 2015 - F - Reunion - - - - - 1 Francois Cartault
+/. 5 c.808C>T r.(?) p.(Arg270Cys) - - Both (homozygous) - pathogenic (recessive) g.177035995C>T g.177608994C>T - - B4GALT7_000003 - PubMed: Cartault 2015, Journal: Cartault 2015 - rs28937869 Germline - - - - - DNA SEQ - - EDS Pat19 PubMed: Cartault 2015, Journal: Cartault 2015 - F - Reunion - - - - - 1 Francois Cartault
+/. 5 c.808C>T r.(?) p.(Arg270Cys) - - Both (homozygous) - pathogenic (recessive) g.177035995C>T g.177608994C>T - - B4GALT7_000003 - PubMed: Cartault 2015, Journal: Cartault 2015 - rs28937869 Germline - - - - - DNA SEQ - - EDS Pat20 PubMed: Cartault 2015, Journal: Cartault 2015 - M - Reunion - - - - - 1 Francois Cartault
+/. 5 c.808C>T r.(?) p.(Arg270Cys) - - Both (homozygous) - pathogenic (recessive) g.177035995C>T g.177608994C>T - - B4GALT7_000003 - PubMed: Cartault 2015, Journal: Cartault 2015 - rs28937869 Germline - - - - - DNA SEQ - - EDS Pat21 PubMed: Cartault 2015, Journal: Cartault 2015 - M - Reunion - - - - - 1 Francois Cartault
+/. 05 c.808C>T r.(?) p.(Arg270Cys) missense substitution Maternal (confirmed) - pathogenic (recessive) g.177035995C>T g.177608994C>T - - B4GALT7_000003 - PubMed: Salter 2016 - - Germline - - - - - DNA SEQ, SEQ-NG - WES trio EDS Pat2 PubMed: Salter 2016 - F - United Kingdom (Great Britain) - - - - - 1 Johan den Dunnen
+/. 05 c.808C>T r.(?) p.(Arg270Cys) missense substitution Maternal (confirmed) - pathogenic (recessive) g.177035995C>T g.177608994C>T - - B4GALT7_000003 - PubMed: Mihalic Mosher 2019 - rs28937869 Germline - - - - - DNA SEQ, SEQ-NG - WES trio EDS patient PubMed: Mihalic Mosher 2019 2-generation family, 3 affected pregnancies, unaffected heterozygous carrier parents - - United States - - - - - 1 Johan den Dunnen
+/+? 5 c.808C>T r.(?) p.(Arg270Cys) missense substitution Paternal (confirmed) - likely pathogenic g.177035995C>T - - - B4GALT7_000003 - PubMed: Sandler-Wilson et al., 2019 - rs28937869 Unknown - - - - - DNA SEQ, SEQ-NG - - EDS, EDSSPD1 - PubMed: Sandler-Wilson et al., 2019 The patient had a female sibling who also carried both variants and was diagnosed with spEDS. The technique used was whole exome sequencing. - - - Partly French - - - - 1 Raymond Dalgleish
+/. - c.808C>T r.(?) p.(Arg270Cys) - - Unknown - pathogenic g.177035995C>T - B4GALT7(NM_007255.2):c.808C>T (p.(Arg270Cys)) - B4GALT7_000003 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.808C>T r.(?) p.(Arg270Cys) - - Both (homozygous) - pathogenic (recessive) g.177035995C>T g.177608994C>T - - B4GALT7_000003 - PubMed: Ranza 2017 - - Germline - - - - - DNA SEQ, SEQ-NG - WES ? Pat12 PubMed: Ranza 2017 patient, family history - yes France - - - - - 1 Johan den Dunnen
-?/. - c.814G>A r.(?) p.(Ala272Thr) - - Unknown - likely benign g.177036001G>A - B4GALT7(NM_007255.2):c.814G>A (p.A272T, p.(Ala272Thr)), B4GALT7(NM_007255.3):c.814G>A (p.A272T) - B4GALT7_000044 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.814G>A r.(?) p.(Ala272Thr) - - Unknown - likely benign g.177036001G>A - B4GALT7(NM_007255.2):c.814G>A (p.A272T, p.(Ala272Thr)), B4GALT7(NM_007255.3):c.814G>A (p.A272T) - B4GALT7_000044 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.814G>A r.(?) p.(Ala272Thr) - - Unknown - likely benign g.177036001G>A - B4GALT7(NM_007255.2):c.814G>A (p.A272T, p.(Ala272Thr)), B4GALT7(NM_007255.3):c.814G>A (p.A272T) - B4GALT7_000044 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-/. - c.828+20T>C r.(=) p.(=) - - Unknown - benign g.177036035T>C g.177609034T>C B4GALT7(NM_007255.3):c.828+20T>C - B4GALT7_000019 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.829G>T r.[829_831del,828_829ins828+1_829-1,829g>u] p.[Glu277del,Gln276_Glu277insVLAGLLIGDR*,Glu277*] - - Both (homozygous) - pathogenic (recessive) g.177036541G>T g.177609540G>T - - B4GALT7_000029 - PubMed: Ritelli 2017 - - Germline - - - - - DNA, RNA RT-PCR, SEQ - - EDS patient PubMed: Ritelli 2017 2-generation family, 1 affected, unaffected heterozygous carrier parents/relatives F - Morocco - - - - - 1 Johan den Dunnen
-?/. - c.867T>C r.(?) p.(Thr289=) - - Unknown - likely benign g.177036579T>C g.177609578T>C B4GALT7(NM_007255.2):c.867T>C (p.T289=) - B4GALT7_000027 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.909C>T r.(?) p.(Gly303=) - - Unknown - likely benign g.177036621C>T g.177609620C>T B4GALT7(NM_007255.2):c.909C>T (p.G303=), B4GALT7(NM_007255.3):c.909C>T (p.G303=) - B4GALT7_000020 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.909C>T r.(?) p.(Gly303=) - - Unknown - likely benign g.177036621C>T - B4GALT7(NM_007255.2):c.909C>T (p.G303=), B4GALT7(NM_007255.3):c.909C>T (p.G303=) - B4GALT7_000020 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. 06 c.970T>A r.(?) p.(Cys324Ser) missense substitution Both (homozygous) - pathogenic (recessive) g.177036682T>A g.177609681T>A - - B4GALT7_000009 - PubMed: Arunrut 2016 - - Germline - - - - - DNA SEQ, SEQ-NG - WES trio EDS patient PubMed: Arunrut 2016 - F - United States - - - - - 1 Johan den Dunnen
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