Variant #0000623635 (NC_000017.10:g.19263689C>T, NM_015681.3:c.76G>A (B9D1))

Chromosome 17
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.19263689C>T
DNA change (hg38) g.19360376C>T
Published as B9D1(NM_001243475.1):c.3G>A (p.M1?)
ISCN -
DB-ID B9D1_000016
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2021-07-29 11:59:40 +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.*26122C>T r.(=) p.(=)
B9D1 NM_015681.3 ?/. - c.76G>A r.(?) p.(Asp26Asn)
MAPK7 NM_139033.2 ?/. - c.-17731C>T r.(?) p.(=)


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