Variant #0000272228 (NC_000012.11:g.7053675C>G, NM_001007026.1:c.*2732C>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.7053675C>G
DNA change (hg38) g.6944512C>G
Published as C12orf57(NM_138425.3):c.89C>G (p.P30R)
ISCN -
DB-ID C12orf57_000003
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 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
ATN1 NM_001007026.1 ?/. - c.*2732C>G - r.(=) p.(=)
PTPN6 NM_002831.5 ?/. - c.-7001C>G - r.(?) p.(=)
C12orf57 NM_138425.2 ?/. - c.89C>G - r.(?) p.(Pro30Arg)


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