Variant #0000711816 (NC_000008.10:g.55541226G>A, NM_006269.1:c.4784G>A (RP1))

Chromosome 8
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.55541226G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID RP1_000017 See all 5 reported entries
Variant remarks -
Reference PubMed: Sohocki 2001
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.01622 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 N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RP1 NM_006269.1 -?/. 4 c.4784G>A r.(?) p.(Arg1595Gln)


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