Variant #0000711820 (NC_000008.10:g.?, NM_006269.1:c.? (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.?
DNA change (hg38) -
Published as AF143222:6098A>G (TAT?TGT) Cys2033Tyr
ISCN -
DB-ID RP1_000000 See all 57 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) Genomic location of variant could not be determined
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




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RP1 NM_006269.1 -?/. - c.? r.(?) p.?


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