Variant #0000304653 (NC_000003.11:g.52561936G>T, NM_015136.2:c.*3564G>T (STAB1))

Chromosome 3
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.52561936G>T
DNA change (hg38) g.52527920G>T
Published as NT5DC2(NM_022908.2):c.733C>A (p.L245M)
ISCN -
DB-ID NT5DC2_000001
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
STAB1 NM_015136.2 ?/. - c.*3564G>T r.(=) p.(=)
NT5DC2 NM_022908.2 ?/. - c.733C>A r.(?) p.(Leu245Met)


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