Variant #0001065678 (NC_000012.11:g.6976669T>G, NM_001098536.1:c.*1428T>G (USP5))

Chromosome 12
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.6976669T>G
DNA change (hg38) -
Published as TPI1(NM_000365.5):c.-62T>G (p.(=))
ISCN -
DB-ID TPI1_000001 See all 2 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) 0.00203 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 2026-01-20 18:57:21 +01:00 (CET)
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.-62T>G r.(?) p.(=)
USP5 NM_001098536.1 -?/. - c.*1428T>G r.(=) p.(=)
SPSB2 NM_032641.3 -?/. - c.*3687A>C r.(=) p.(=)


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