Variant #0000316923 (NC_000009.11:g.32543285T>G, NM_005802.4:c.1238A>C (TOPORS))

Chromosome 9
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.32543285T>G
DNA change (hg38) g.32543287T>G
Published as TOPORS(NM_005802.4):c.1238A>C (p.Q413P), TOPORS(NM_005802.5):c.1238A>C (p.Q413P)
ISCN -
DB-ID TOPORS_000009 See all 3 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) 0.00156 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-02-26 20:06:56 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TOPORS NM_005802.4 ?/. - c.1238A>C r.(?) p.(Gln413Pro)


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