Variant #0000761493 (NC_000006.11:g.42689632del, NM_000322.4:c.441del (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.42689632del
DNA change (hg38) g.42721894del
Published as -
ISCN -
DB-ID PRPH2_000002 See all 31 reported entries
Variant remarks ACMG PVS1, PS4, PM1, PP1
Reference PubMed: Peeters 2021, Journal: Peeters 2021
ClinVar ID -
dbSNP ID rs61755784
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 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)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PRPH2 NM_000322.4 +/. 1 c.441del r.(?) p.(Gly148Alafs*5)


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