Variant #0000980453 (NC_000012.11:g.7053271G>C, NM_001007026.1:c.*2328G>C (ATN1))

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.7053271G>C
DNA change (hg38) -
Published as C12orf57(NM_001301834.1):c.-14G>C
ISCN -
DB-ID C12orf57_000045
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) 0.0003 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
ATN1 NM_001007026.1 ?/. - c.*2328G>C - r.(=) p.(=)
PTPN6 NM_002831.5 ?/. - c.-7405G>C - r.(?) p.(=)
C12orf57 NM_138425.2 ?/. - c.-14G>C - r.(?) p.(=)


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