Variant #0000571615 (NC_000022.10:g.26849247G>A, NM_022081.5:c.2079C>T (HPS4))

Chromosome 22
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.26849247G>A
DNA change (hg38) g.26453281G>A
Published as HPS4(NM_001349903.2):c.1837C>T (p.R613W), HPS4(NM_022081.5):c.2079C>T (p.S693=)
ISCN -
DB-ID HPS4_000029 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) 0.00447 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 2022-05-09 15:51:19 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HPS4 NM_022081.5 -?/. - c.2079C>T r.(?) p.(Ser693=)


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