Variant #0000577888 (NC_000024.9:g.14832537T>A, NM_004654.3:c.112T>A (USP9Y))

Chromosome Y
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.14832537T>A
DNA change (hg38) g.12720604T>A
Published as USP9Y(NM_004654.3):c.112T>A (p.(Ser38Thr))
ISCN -
DB-ID USP9Y_000026
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
USP9Y NM_004654.3 -?/. - c.112T>A r.(?) p.(Ser38Thr)


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