Variant #0000529252 (NC_000006.11:g.56495124T>C, NM_001723.5:c.2589A>G (DST))

Chromosome 6
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.56495124T>C
DNA change (hg38) g.56630326T>C
Published as DST(NM_001144769.5):c.4101A>G (p.K1367=)
ISCN -
DB-ID DST_000196
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) 0.00211 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 2019-07-18 18:22:55 +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_001374736.1 -/. - c.4200A>G r.(?) p.(Lys1400=)
DST NM_001723.5 -/. - c.2589A>G r.(?) p.(Lys863=)


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