Variant #0000711813 (NC_000006.11:g.42666061T>C, NM_000322.4:c.1013A>G (PRPH2))

Chromosome 6
Allele Parent #1
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.42666061T>C
DNA change (hg38) -
Published as 1014G>A (GGC?GAC) Gly338Asp
ISCN -
DB-ID PRPH2_000003 See all 16 reported entries
Variant remarks -
Reference PubMed: Sohocki 2001
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency 0.22
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.77653 View details
Owner Julia Lopez
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Julia Lopez
Date created 2021-01-14 12:40:33 +01:00 (CET)
Date last edited 2021-10-29 16:57:32 +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 -?/. - c.1013A>G r.(?) p.(Asp338Gly)


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