Variant #0000548767 (NC_000012.11:g.57637942del, NM_005412.5:c.*9798del (SHMT2))

Chromosome 12
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.57637942del
DNA change (hg38) g.57244159del
Published as STAC3(NM_145064.2):c.925delC (p.R309Vfs*5)
ISCN -
DB-ID NDUFA4L2_000002
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-02 16:34:51 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SHMT2 NM_005412.5 ?/. - c.*9798del r.(?) p.(=)
NDUFA4L2 NM_020142.3 ?/. - c.-3661del r.(?) p.(=)
STAC3 NM_145064.1 ?/. - c.925del r.(?) p.(Arg309ValfsTer5)


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