Variant #0000644084 (NC_000014.8:g.77920368G>A, NM_022067.3:c.78C>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.77920368G>A
DNA change (hg38) g.77454025G>A
Published as c.2T>G (p.(Met1Arg))
ISCN -
DB-ID VIPAS39_000010
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs112217896
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 6.0E-5 View details
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)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
VIPAS39 NM_022067.3 ?/? 1 c.78C>T r.(?) p.(=)


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