Variant #0000854782 (NC_000017.10:g.19247049C>T, NC_000017.10(NM_015681.3):c.472+54G>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.19247049C>T
DNA change (hg38) -
Published as B9D1(NM_001321215.1):c.526G>A (p.E176K)
ISCN -
DB-ID EPN2_000003
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 2022-05-09 15:47:41 +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.*9482C>T r.(=) p.(=)
B9D1 NM_015681.3 ?/. - c.472+54G>A r.(=) p.(=)
MAPK7 NM_139033.2 ?/. - c.-34371C>T r.(?) p.(=)


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