Variant #0000724222 (NC_000012.11:g.7045912_7045938dup, NM_001007026.1:c.1482_1508dup (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.7045912_7045938dup
DNA change (hg38) -
Published as ATN1(NM_001007026.2):c.1482_1508dupGCAGCAGCAGCAGCAGCAGCAGCAGCA (p.Q494_Q502dup)
ISCN -
DB-ID ATN1_000139
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 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
ATN1 NM_001007026.1 ?/. - c.1482_1508dup - r.(?) p.(Gln494_Gln502dup)


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