Variant #0000549097 (NC_000012.11:g.7054961A>G, NM_001007026.1:c.*4018A>G (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.7054961A>G
DNA change (hg38) g.6945798A>G
Published as C12orf57(NM_138425.4):c.257A>G (p.(Lys86Arg))
ISCN -
DB-ID C12orf57_000011
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) 0.00057 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +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.*4018A>G - r.(=) p.(=)
PTPN6 NM_002831.5 ?/. - c.-5715A>G - r.(?) p.(=)
C12orf57 NM_138425.2 ?/. - c.257A>G - r.(?) p.(Lys86Arg)


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