Variant #0000549702 (NC_000013.10:g.103514786T>C, NM_001204425.1:c.2649T>C (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.103514786T>C
DNA change (hg38) g.102862436T>C
Published as ERCC5(NM_000123.3):c.1287T>C (p.D429=)
ISCN -
DB-ID BIVM_000006
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) 0.00076 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 2019-07-18 18:22:55 +02:00 (CEST)
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.1287T>C r.(?) p.(Asp429=)
BIVM NM_001159596.1 -?/. - c.*22571T>C r.(=) p.(=)
BIVM-ERCC5 NM_001204425.1 -?/. - c.2649T>C r.(?) p.(Asp883=)


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