Variant #0000253110 (NC_000012.11:g.49691250A>G, NM_006262.3:c.1107A>G (PRPH))

Chromosome 12
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.49691250A>G
DNA change (hg38) g.49297467A>G
Published as PRPH(NM_006262.3):c.1107A>G (p.K369=), PRPH(NM_006262.4):c.1107A>G (p.K369=)
ISCN -
DB-ID PRPH_000012 See all 3 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) 0.1913 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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     
TROAP NM_005480.3 -/. - c.-25888A>G r.(?) p.(=)
PRPH NM_006262.3 -/. - c.1107A>G r.(?) p.(Lys369=)


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