Variant #0000532476 (NC_000007.13:g.66459273T>A, NM_016038.2:c.184A>T (SBDS))

Chromosome 7
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.66459273T>A
DNA change (hg38) g.66994286T>A
Published as SBDS(NM_016038.2):c.184A>T (p.K62*, p.(Lys62*)), SBDS(NM_016038.4):c.184A>T (p.K62*)
ISCN -
DB-ID SBDS_000007 See all 6 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) 0.00014 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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     
SBDS NM_016038.2 +/. - c.184A>T r.(?) p.(Lys62Ter)
TYW1 NM_018264.2 +/. - c.-2693T>A r.(?) p.(=)


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