Variant #0000927588 (NC_000010.10:g.104309821G>A, NM_016169.3:c.412G>A (SUFU))

Chromosome 10
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.104309821G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID SUFU_000033 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs34406289
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00022 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2023-05-09 15:04:01 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SUFU NM_016169.3 ?/. - c.412G>A r.(?) p.(Ala138Thr)


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