Variant #0000993814 (NC_000003.11:g.52549487C>T, NM_015136.2:c.3913C>T (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.52549487C>T
DNA change (hg38) -
Published as STAB1(NM_015136.2):c.3913C>T (p.(Arg1305Trp))
ISCN -
DB-ID NT5DC2_000015
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) 1.0E-5 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 2024-08-28 13:16:32 +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.3913C>T r.(?) p.(Arg1305Trp)
NT5DC2 NM_022908.2 -?/. - c.*8999G>A r.(=) p.(=)


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