Variant #0000761552 (NC_000006.11:g.42690069C>A, NM_000322.4:c.4G>T (PRPH2))

Chromosome 6
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method ACMG
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.42690069C>A
DNA change (hg38) g.42722331C>A
Published as -
ISCN -
DB-ID PRPH2_000147 See all 2 reported entries
Variant remarks ACMG PM2, PP3; ACMG criteria not strong enough to label as pathogenic
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) Retrieve
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)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PRPH2 NM_000322.4 ?/. 1 c.4G>T r.(?) p.(Ala2Ser)


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