Variant #0000529253 (NC_000006.11:g.56498994C>T, NM_001723.5:c.1946G>A (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.56498994C>T
DNA change (hg38) g.56634196C>T
Published as DST(NM_001144769.2):c.3458G>A (p.S1153N), DST(NM_001144769.5):c.3458G>A (p.S1153N)
ISCN -
DB-ID DST_000032 See all 2 reported entries
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) 0.00132 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_001723.5 -?/. - c.1946G>A r.(?) p.(Ser649Asn)


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