Variant #0000276289 (NC_000013.10:g.103519083C>T, NM_001204425.1:c.3783C>T (BIVM-ERCC5))

Chromosome 13
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.103519083C>T
DNA change (hg38) g.102866733C>T
Published as ERCC5(NM_000123.3):c.2421C>T (p.I807=)
ISCN -
DB-ID ERCC5_000041
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) 5.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ERCC5 NM_000123.2 -?/. - c.2421C>T r.(?) p.(Ile807=)
BIVM NM_001159596.1 -?/. - c.*26868C>T r.(=) p.(=)
BIVM-ERCC5 NM_001204425.1 -?/. - c.3783C>T r.(?) p.(Ile1261=)


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