Variant #0000850386 (NC_000003.11:g.52567566G>C, NM_015136.2:c.*9194G>C (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.52567566G>C
DNA change (hg38) -
Published as NT5DC2(NM_001134231.2):c.188C>G (p.A63G)
ISCN -
DB-ID NT5DC2_000008
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) 0.00019 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited 2023-08-04 19:32:37 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SMIM4 NM_001124767.1 -?/. - c.-3206G>C r.(?) p.(=)
STAB1 NM_015136.2 -?/. - c.*9194G>C r.(=) p.(=)
NT5DC2 NM_022908.2 -?/. - c.121+983C>G r.(=) p.(=)


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