Variant #0000930706 (NC_000017.10:g.19265863C>A, NM_015681.3:c.20G>T (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.19265863C>A
DNA change (hg38) -
Published as B9D1(NM_015681.6):c.20G>T (p.S7I)
ISCN -
DB-ID EPN2_000010
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-07-07 10:10:56 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EPN2 NM_014964.4 ?/. - c.*28296C>A r.(=) p.(=)
B9D1 NM_015681.3 ?/. - c.20G>T r.(?) p.(Ser7Ile)
MAPK7 NM_139033.2 ?/. - c.-15557C>A r.(?) p.(=)


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