Variant #0000323476 (NC_000013.10:g.103525656C>T, NM_001204425.1:c.4289C>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.103525656C>T
DNA change (hg38) g.102873306C>T
Published as BIVM-ERCC5(NM_001204425.1):c.4289C>T (p.(Ser1430Phe))
ISCN -
DB-ID ERCC5_000051
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ERCC5 NM_000123.2 ?/. - c.2927C>T r.(?) p.(Ser976Phe)
BIVM NM_001159596.1 ?/. - c.*33441C>T r.(=) p.(=)
BIVM-ERCC5 NM_001204425.1 ?/. - c.4289C>T r.(?) p.(Ser1430Phe)


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