Variant #0000949362 (NC_000010.10:g.124221250G>A, NM_002775.4:c.82G>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.124221250G>A
DNA change (hg38) -
Published as HTRA1(NM_002775.4):c.82G>A (p.(Gly28Ser))
ISCN -
DB-ID ARMS2_000009
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2023-11-27 17:35:39 +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     
ARMS2 NM_001099667.1 -?/. - c.*4801G>A r.(=) p.(=)
HTRA1 NM_002775.4 -?/. - c.82G>A r.(?) p.(Gly28Ser)


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