Variant #0000644093 (NC_000014.8:g.77893431G>A, NM_022067.3:c.*528C>T (VIPAS39))

Chromosome 14
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.77893431G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID VIPAS39_000016
Variant remarks Variant Error [EREF/EREF]: This genomic variant does not match the reference sequence; the transcript variant does not match the reference sequence either. Please fix this entry and then remove this message.
Reference -
ClinVar ID -
dbSNP ID rs8009177
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Paul Gissen
Database submission license No license selected
Created by Paul Gissen
Date created 2011-08-22 13:28:12 +02:00 (CEST)
Date last edited 2021-09-09 14:41:03 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
VIPAS39 NM_022067.3 ?/? UTR c.*528C>T r.? p.(=)


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