Variant #0000548963 (NC_000012.11:g.64784211_64784212insTA, NM_001099676.2:c.135_136insAT (C12orf56))

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.64784211_64784212insTA
DNA change (hg38) g.64390431_64390432insTA
Published as C12orf56(NM_001170633.1):c.135_136insAT (p.E46Mfs*11)
ISCN -
DB-ID C12orf56_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 16:54:14 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C12orf56 NM_001099676.2 ?/. - c.135_136insAT r.(?) p.(Glu46MetfsTer11)


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