Full data view for gene CHM


This database is one of the ”Retinal and hearing impairment genetic variant databases”.
Information The variants shown are described using the NM_000390.2 transcript reference sequence.

9 entries on 1 page. Showing entries 1 - 9.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     

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     
+/+ 5 c.315_318del r.(?) p.(Ser105Argfs*20) - Maternal (inferred) - pathogenic g.85219056_85219059del g.85964051_85964054del 345_348del - CHM_000018 hemizygous PubMed: Fujiki 1999 - - Germline - - -BsrI - - DNA SEQ - - CHM - PubMed: Fujiki 1999 - M - Japan - - - - - 1 David Baux
+/+ 5 c.315_318del r.(?) p.(Ser105Argfs*20) - Unknown - pathogenic g.85219056_85219059del g.85964051_85964054del 345_348del - CHM_000018 hemizygous PubMed: Mc Taggart 2002 - - Germline - - -BsrI - - DNA SEQ - - CHM - PubMed: Mc Taggart 2002 - M - - - - - - - 1 David Baux
+/+ 5 c.315_318del r.315_318del p.Ser105Argfs*20 - Maternal (confirmed) - pathogenic g.85219056_85219059del g.85964051_85964054del 345_348del - CHM_000018 hemizygous; Characterized at mRNA level PubMed: Esposito 2011 - - Germline - - -BsrI - - DNA, RNA, protein PCR, PTT, RT-PCR, SEQ - - CHM - PubMed: Esposito 2011 - M - Italy - - - - - 1 Francesco Salvatore
+/+ 5 c.315_318del r.(?) p.(Ser105Argfs*20) - Unknown - pathogenic g.85219056_85219059del g.85964051_85964054del 345_348del - CHM_000018 hemizygous PubMed: Aleman TS 2017 - - Germline - - -BsrI - - DNA SEQ - - CHM - PubMed: Aleman TS 2017 - - - - - - - - - 1 David Baux
+/. 5 c.315_318del r.(?) p.(Ser105Argfs*20) - Parent #1 - pathogenic (dominant) g.85219056_85219059del g.85964051_85964054del - - CHM_000018 - Zeitz 2021, submitted - - Germline - - - - - DNA SEQ - - CHM Fam3841PatCIC06996 Zeitz 2021, submitted - - - France - - - - - 1 Christina Zeitz
+?/. - c.315_318del r.(?) p.(Ser105Argfs*20) - Parent #1 - likely pathogenic g.85219056_85219059del g.85964051_85964054del CHM, variant 1: c.315_318del/p.S105Rfs*20 - CHM_000018 solved, hemizygous PubMed: Weisschuh 2020 - - Germline yes - - - - DNA SEQ blood Sanger sequencing retinal disease 89 PubMed: Weisschuh 2020 Filing key number: 44, choroideremia, no patient Ids, consecutive numbers given M - Germany - - - - - 1 LOVD
+?/. - c.315_318del r.(?) p.(Ser105Argfs*20) - Parent #1 - likely pathogenic g.85219056_85219059del g.85964051_85964054del CHM, variant 1: c.315_318del/p.S105Rfs*20 - CHM_000018 solved, hemizygous PubMed: Weisschuh 2020 - - Germline yes - - - - DNA SEQ blood Sanger sequencing retinal disease 90 PubMed: Weisschuh 2020 Filing key number: 44, choroideremia, no patient Ids, consecutive numbers given M - Germany - - - - - 1 LOVD
+/. 5 c.315_318del r.(?) p.(Ser105Argfs*20) - Maternal (inferred) - pathogenic g.85219054_85219057del - c.315_318del - CHM_000018 - PubMed: Mucciolo 2019 - - Germline - - - - - DNA ? - - retinal disease P4 PubMed: Mucciolo 2019 - - - - - - - - - 1 LOVD
+/. 5 c.315_318del r.(?) p.(Ser105Argfs*20) - Maternal (inferred) - pathogenic g.85219054_85219057del - c.315_318del - CHM_000018 - PubMed: Hayashi 2020 - - Germline - - - - - DNA SEQ blood - retinal disease F8-JU1059 PubMed: Hayashi 2020 - M - Japan Japanese - - - - 1 LOVD
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