Variant #0000322654 (NC_000012.11:g.7053317G>C, NM_001007026.1:c.*2374G>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.7053317G>C
DNA change (hg38) g.6944154G>C
Published as C12orf57(NM_138425.2):c.33G>C (p.(Leu11Phe)), C12orf57(NM_138425.4):c.33G>C (p.L11F)
ISCN -
DB-ID C12orf57_000002 See all 2 reported entries
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) 4.0E-5 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
ATN1 NM_001007026.1 ?/. - c.*2374G>C - r.(=) p.(=)
PTPN6 NM_002831.5 ?/. - c.-7359G>C - r.(?) p.(=)
C12orf57 NM_138425.2 ?/. - c.33G>C - r.(?) p.(Leu11Phe)


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