Variant #0000865112 (NC_000017.10:g.19261225G>A, NM_015681.3:c.172C>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.19261225G>A
DNA change (hg38) -
Published as B9D1(NM_001243473.1):c.231C>T (p.(Ala77=))
ISCN -
DB-ID EPN2_000005
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 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2022-05-09 16:01:56 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +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.*23658G>A r.(=) p.(=)
B9D1 NM_015681.3 ?/. - c.172C>T r.(?) p.(Gln58*)
MAPK7 NM_139033.2 ?/. - c.-20195G>A r.(?) p.(=)


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