Variant #0001043784 (NC_000022.10:g.26875323T>A, NC_000022.10(NM_022081.5):c.42-2A>T (HPS4))

Chromosome 22
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.26875323T>A
DNA change (hg38) -
Published as HPS4(NM_022081.6):c.42-2A>T
ISCN -
DB-ID SRRD_000004
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TFIP11 NM_001008697.1 +?/. - c.*12656A>T r.(=) p.(=)
SRRD NM_001013694.2 +?/. - c.-4534T>A r.(?) p.(=)
HPS4 NM_022081.5 +?/. - c.42-2A>T r.spl? p.?


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