Variant #0000761550 (NC_000006.11:g.42690035C>T, NM_000322.4:c.38G>A (PRPH2))

Chromosome 6
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method ACMG
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.42690035C>T
DNA change (hg38) g.42722297C>T
Published as -
ISCN -
DB-ID PRPH2_000294 See all 3 reported entries
Variant remarks ACMG PS4, PM5, PP3
Reference PubMed: Peeters 2021, Journal: Peeters 2021
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner LOVD
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Manon Peeters
Date created 2021-04-06 12:57:06 +02:00 (CEST)
Date last edited 2021-10-29 16:20:22 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PRPH2 NM_000322.4 +?/. 1 c.38G>A r.(?) p.(Arg13Gln)


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