Variant #0000263499 (NC_000017.10:g.19265952C>T, NM_015681.3:c.-70G>A (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.19265952C>T
DNA change (hg38) g.19362639C>T
Published as B9D1(NM_001243473.1):c.83G>A (p.R28K)
ISCN -
DB-ID B9D1_000009 See all 3 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) 0.02852 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 2025-08-03 21:38:54 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EPN2 NM_014964.4 -/. - c.*28385C>T r.(=) p.(=)
B9D1 NM_015681.3 -/. - c.-70G>A r.(?) p.(=)
MAPK7 NM_139033.2 -/. - c.-15468C>T r.(?) p.(=)


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