Variant #0000805927 (NC_000012.11:g.6978545G>T, NM_001098536.1:c.*3304G>T (USP5))

Chromosome 12
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.6978545G>T
DNA change (hg38) -
Published as TPI1(NM_000365.6):c.448G>T (p.V150F)
ISCN -
DB-ID SPSB2_000003
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) 0.00054 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2021-09-17 14:40:49 +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     
TPI1 NM_000365.5 ?/. - c.448G>T r.(?) p.(Val150Phe)
USP5 NM_001098536.1 ?/. - c.*3304G>T r.(=) p.(=)
SPSB2 NM_032641.3 ?/. - c.*1811C>A r.(=) p.(=)


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