Variant #0000532477 (NC_000007.13:g.66460278C>A, NM_016038.2:c.127G>T (SBDS))

Chromosome 7
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.66460278C>A
DNA change (hg38) g.66995291C>A
Published as SBDS(NM_016038.2):c.127G>T (p.(Val43Leu), p.V43L)
ISCN -
DB-ID SBDS_000010 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) 0.00118 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 2022-11-01 13:01:21 +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.127G>T r.(?) p.(Val43Leu)
TYW1 NM_018264.2 -?/. - c.-1688C>A r.(?) p.(=)


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