Variant #0000913948 (NC_000012.11:g.7053266C>T, NM_001007026.1:c.*2323C>T (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.7053266C>T
DNA change (hg38) -
Published as C12orf57(NM_138425.4):c.-19C>T
ISCN -
DB-ID C12orf57_000036
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-01-11 15:44:22 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
ATN1 NM_001007026.1 ?/. - c.*2323C>T - r.(=) p.(=)
PTPN6 NM_002831.5 ?/. - c.-7410C>T - r.(?) p.(=)
C12orf57 NM_138425.2 ?/. - c.-19C>T - r.(?) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.