Variant #0000283445 (NC_000010.10:g.124266187G>A, NC_000010.10(NM_002775.4):c.778-20G>A (HTRA1))

Chromosome 10
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.124266187G>A
DNA change (hg38) g.122506671G>A
Published as HTRA1(NM_002775.4):c.778-20G>A (p.(=)), HTRA1(NM_002775.5):c.778-20G>A
ISCN -
DB-ID HTRA1_000012 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) 0.01057 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HTRA1 NM_002775.4 -?/. - c.778-20G>A r.(=) p.(=)


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