Variant #0000247789 (NC_000023.10:g.46696624A>G, NM_006915.2:c.89A>G (RP2))

Chromosome X
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.46696624A>G
DNA change (hg38) g.46837189A>G
Published as RP2(NM_006915.2):c.89A>G (p.(Asp30Gly)), RP2(NM_006915.3):c.89A>G (p.D30G)
ISCN -
DB-ID RP2_000011 See all 2 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RP2 NM_006915.2 ?/. - c.89A>G r.(?) p.(Asp30Gly)


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