Variant #0000263455 (NC_000023.10:g.13337614C>T, ATXN3L(NM_001135995.1):c.440G>A)

Chromosome X
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.13337614C>T
DNA change (hg38) g.13319495C>T
Published as ATXN3L(NM_001135995.1):c.440G>A (p.C147Y)
ISCN -
DB-ID ATXN3L_000005
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) 0.00039 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ATXN3L NM_001135995.1 -?/. - c.440G>A r.(?) p.(Cys147Tyr)