Variant #0000692286 (NC_000017.10:g.19265917G>A, NM_015681.3:c.-35C>T (B9D1))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.19265917G>A
DNA change (hg38) -
Published as B9D1(NM_001243473.1):c.118C>T (p.P40S)
ISCN -
DB-ID B9D1_000020
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) 7.0E-5 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 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +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.*28350G>A r.(=) p.(=)
B9D1 NM_015681.3 -?/. - c.-35C>T r.(?) p.(=)
MAPK7 NM_139033.2 -?/. - c.-15503G>A r.(?) p.(=)


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