Variant #0000538832 (NC_000010.10:g.100189636C>T, NM_000195.3:c.779G>A (HPS1))

Chromosome 10
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.100189636C>T
DNA change (hg38) g.98429879C>T
Published as HPS1(NM_000195.3):c.779G>A (p.(Arg260Gln)), HPS1(NM_000195.5):c.779G>A (p.R260Q), HPS1(NM_001322477.1):c.779G>A (p.R260Q)
ISCN -
DB-ID HPS1_000012 See all 3 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) 0.00163 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HPS1 NM_000195.3 -/. - c.779G>A r.(?) p.(Arg260Gln)


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