Variant #0000644101 (NC_000014.8:g.77908954A>G, NM_022067.3:c.683T>C (VIPAS39))

Chromosome 14
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Probably does not affect function
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.77908954A>G
DNA change (hg38) g.77442611A>G
Published as -
ISCN -
DB-ID VIPAS39_000018
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
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 2011-09-27 16:10:28 +02:00 (CEST)
Date last edited 2021-09-09 14:48:34 +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 -?/-? 9 c.683T>C r.(?) p.(Ile228Thr)


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