Variant #0001006206 (NC_000022.10:g.45255629G>C, NM_001017528.2:c.*122502G>C (PRR5))

Chromosome 22
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.45255629G>C
DNA change (hg38) -
Published as ARHGAP8(NM_181335.2):c.896G>C (p.(Arg299Pro))
ISCN -
DB-ID PRR5-ARHGAP8_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) 0.00012 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +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     
ARHGAP8 NM_001017526.1 ?/. - c.989G>C r.(?) p.(Arg330Pro)
PRR5 NM_001017528.2 ?/. - c.*122502G>C r.(=) p.(=)
PRR5-ARHGAP8 NM_181334.4 ?/. - c.1262G>C r.(?) p.(Arg421Pro)


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