Variant #0000761498 (NC_000006.11:g.42689651T>C, NM_000322.4:c.422A>G (PRPH2))

Chromosome 6
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method ACMG
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.42689651T>C
DNA change (hg38) g.42721913T>C
Published as -
ISCN -
DB-ID PRPH2_000105 See all 67 reported entries
Variant remarks ACMG PS3, PM1, PM2,PP1, PP3
Reference PubMed: Peeters 2021, Journal: Peeters 2021
ClinVar ID -
dbSNP ID rs61755781
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.422A>G r.(?) p.(Tyr141Cys)


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