Variant #0000975928 (NC_000003.11:g.52556865G>A, NM_015136.2:c.6819G>A (STAB1))

Chromosome 3
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.52556865G>A
DNA change (hg38) -
Published as STAB1(NM_015136.3):c.6819G>A (p.(Ala2273=))
ISCN -
DB-ID NT5DC2_000011
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) 0.00071 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 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
STAB1 NM_015136.2 -?/. - c.6819G>A r.(?) p.(=)
NT5DC2 NM_022908.2 -?/. - c.*1621C>T r.(=) p.(=)


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