Variant #0000258485 (NC_000012.11:g.111894072C>T, NC_000012.11(NM_002973.3):c.3517-12G>A (ATXN2))

Chromosome 12
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.111894072C>T
DNA change (hg38) g.111456268C>T
Published as ATXN2(NM_002973.4):c.3037-12G>A
ISCN -
DB-ID ATXN2_000011 See all 2 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) 0.20981 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
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     
ATXN2 NM_002973.3 -/. - c.3517-12G>A - r.(=) p.(=)
SH2B3 NM_005475.2 -/. - c.*7966C>T - r.(=) p.(=)


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