Variant #0000890863 (NC_000013.10:g.103508441G>T, NM_001204425.1:c.1869G>T (BIVM-ERCC5))

Chromosome 13
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.103508441G>T
DNA change (hg38) -
Published as ERCC5(NM_000123.4):c.507G>T (p.M169I)
ISCN -
DB-ID BIVM_000037
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BIVM NM_001159596.1 ?/. - c.*16226G>T r.(=) p.(=)
BIVM-ERCC5 NM_001204425.1 ?/. - c.1869G>T r.(?) p.(Met623Ile)


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