Variant #0000017968 (NC_000002.11:g.74759825G>A, NM_013247.4:c.1195G>A (HTRA2))

Chromosome 2
Allele Parent #1
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.74759825G>A
DNA change (hg38) g.74532698G>A
Published as -
ISCN -
DB-ID HTRA2_000001 See all 5 reported entries
Variant remarks variant marked as interesting (probably affects the function of the gene with phenotypic consequences) from an exome analysis. Please contact me.
Reference -
ClinVar ID -
dbSNP ID -
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP 1
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00404 View details
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2013-05-06 09:44:15 +02:00 (CEST)
Date last edited 2014-07-03 11:48:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HTRA2 NM_013247.4 ?/? ? c.1195G>A r.(?) p.(Gly399Ser)


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