Variant #0000344977 (NC_000010.10:g.98743566C>T, NM_015652.2:c.2419C>T (C10orf12))

Chromosome 10
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.98743566C>T
DNA change (hg38) g.96983809C>T
Published as -
ISCN -
DB-ID C10orf12_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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-29 09:40:30 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LCOR NM_001170765.1 ?/. - c.*27887C>T r.(=) p.(=)
C10orf12 NM_015652.2 ?/. - c.2419C>T r.(?) p.(Gln807Ter)


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