Variant #0000329079 (NC_000022.10:g.45133122G>A, NM_001017528.2:c.1135G>A (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.45133122G>A
DNA change (hg38) g.44737242G>A
Published as PRR5(NM_001017528.2):c.1135G>A (p.(Val379Met))
ISCN -
DB-ID PRR5-ARHGAP8_000003
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) 3.0E-5 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARHGAP8 NM_001017526.1 ?/. - c.-15457G>A r.(?) p.(=)
PRR5 NM_001017528.2 ?/. - c.1135G>A r.(?) p.(Val379Met)
PRR5-ARHGAP8 NM_181334.4 ?/. - c.295+10608G>A r.(=) p.(=)


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