Variant #0000926409 (NC_000017.10:g.19261216G>A, NM_015681.3:c.181C>T (B9D1))

Chromosome 17
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.19261216G>A
DNA change (hg38) -
Published as B9D1(NM_001321218.2):c.181C>T (p.R61W)
ISCN -
DB-ID EPN2_000008
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) 0.00249 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 2023-04-16 21:50:28 +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     
EPN2 NM_014964.4 -/. - c.*23649G>A r.(=) p.(=)
B9D1 NM_015681.3 -/. - c.181C>T r.(?) p.(Arg61Trp)
MAPK7 NM_139033.2 -/. - c.-20204G>A r.(?) p.(=)


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