Variant #0000891906 (NC_000014.8:g.77919702C>T, NM_022067.3:c.136G>A (VIPAS39))

Chromosome 14
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.77919702C>T
DNA change (hg38) -
Published as VIPAS39(NM_022067.4):c.136G>A (p.V46M)
ISCN -
DB-ID AHSA1_000002 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) 0.00167 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-11-01 13:01:21 +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     
AHSA1 NM_012111.2 -?/. - c.-4831C>T r.(?) p.(=)
VIPAS39 NM_022067.3 -?/. - c.136G>A r.(?) p.(Val46Met)


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