Variant #0000527959 (NC_000006.11:g.16327906_16327908dup, NM_000332.3:c.675_677dup (ATXN1))

Chromosome 6
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.16327906_16327908dup
DNA change (hg38) g.16327675_16327677dup
Published as ATXN1(NM_000332.3):c.672_674dup (p.(Gln225dup)), ATXN1(NM_000332.3):c.675_677dupGCA (p.Q225dup), ATXN1(NM_000332.4):c.675_677dupGCA (p.Q225dup)
ISCN -
DB-ID ATXN1_000004 See all 16 reported entries
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
ATXN1 NM_000332.3 -?/. - c.675_677dup - r.(?) p.(Gln225dup)


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