Variant #0000851267 (NC_000006.11:g.56819347G>A, NM_001723.5:c.-311761C>T (DST))

Chromosome 6
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.56819347G>A
DNA change (hg38) -
Published as DST(NM_001144769.5):c.39C>T (p.Y13=)
ISCN -
DB-ID BEND6_000009
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) 3.0E-5 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DST NM_001723.5 -?/. - c.-311761C>T r.(?) p.(=)
BEND6 NM_152731.2 -?/. - c.-1012G>A r.(?) p.(=)


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