Variant #0000723849 (NC_000012.11:g.113629192C>T, NM_032848.1:c.380C>T (C12orf52))

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.113629192C>T
DNA change (hg38) -
Published as RITA1(NM_001286215.1):c.452C>T (p.P151L)
ISCN -
DB-ID C12orf52_000005
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 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C12orf52 NM_032848.1 ?/. - c.380C>T r.(?) p.(Pro127Leu)
IQCD NM_138451.1 ?/. - c.*4188G>A r.(=) p.(=)


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