Variant #0001065682 (NC_000012.11:g.7053021_7053022insT, NM_001007026.1:c.*2078_*2079insT (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.7053021_7053022insT
DNA change (hg38) -
Published as -
ISCN -
DB-ID C12orf57_000054
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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2026-01-20 18:57:21 +01:00 (CET)
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.*2078_*2079insT - r.(=) p.(=)
PTPN6 NM_002831.5 -?/. - c.-7655_-7654insT - r.(?) p.(=)
C12orf57 NM_138425.2 -?/. - c.-264_-263insT - r.(?) p.(=)
RNU7-1 NR_023317.1 -?/. - n.43_44insT - r.(?) -


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