Variant #0000329081 (NC_000022.10:g.45258353C>A, NM_001017528.2:c.*125226C>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.45258353C>A
DNA change (hg38) g.44862473C>A
Published as ARHGAP8(NM_001017526.1):c.1273C>A (p.(Pro425Thr))
ISCN -
DB-ID PRR5-ARHGAP8_000006
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_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)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARHGAP8 NM_001017526.1 ?/. - c.1273C>A r.(?) p.(Pro425Thr)
PRR5 NM_001017528.2 ?/. - c.*125226C>A r.(=) p.(=)
PRR5-ARHGAP8 NM_181334.4 ?/. - c.1546C>A r.(?) p.(Pro516Thr)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.