Variant #0000691426 (NC_000012.11:g.7053685A>G, NM_001007026.1:c.*2742A>G (ATN1))

Chromosome 12
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.7053685A>G
DNA change (hg38) -
Published as C12orf57(NM_138425.3):c.99A>G (p.A33=)
ISCN -
DB-ID C12orf57_000015
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) 6.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-09-15 15:50:26 +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.*2742A>G - r.(=) p.(=)
PTPN6 NM_002831.5 -?/. - c.-6991A>G - r.(?) p.(=)
C12orf57 NM_138425.2 -?/. - c.99A>G - r.(?) p.(Ala33=)


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