Variant #0000861774 (NC_000009.11:g.98735109G>C, NM_001010895.2:c.*6107G>C (ERCC6L2))

Chromosome 9
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.98735109G>C
DNA change (hg38) -
Published as ERCC6L2(NM_020207.4):c.3109G>C (p.V1037L), ERCC6L2(NM_020207.5):c.3109G>C (p.V1037L)
ISCN -
DB-ID ERCC6L2_000006 See all 2 reported entries
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) 0.00125 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ERCC6L2 NM_001010895.2 -?/. - c.*6107G>C r.(=) p.(=)


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