Variant #0000247703 (NC_000022.10:g.26875240A>G, NM_022081.5:c.123T>C (HPS4))

Chromosome 22
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.26875240A>G
DNA change (hg38) g.26479274A>G
Published as HPS4(NM_022081.6):c.123T>C (p.Y41=)
ISCN -
DB-ID HPS4_000028
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 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
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     
TFIP11 NM_001008697.1 -/. - c.*12739T>C r.(=) p.(=)
SRRD NM_001013694.2 -/. - c.-4617A>G r.(?) p.(=)
HPS4 NM_022081.5 -/. - c.123T>C r.(?) p.(Tyr41=)


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