Variant #0000306472 (NC_000020.10:g.62664263G>A, NM_012469.3:c.2743G>A (PRPF6))

Chromosome 20
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.62664263G>A
DNA change (hg38) g.64032910G>A
Published as PRPF6(NM_012469.3):c.2743G>A (p.V915M), PRPF6(NM_012469.4):c.2743G>A (p.V915M)
ISCN -
DB-ID PRPF6_000024 See all 4 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) 0.00064 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 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PRPF6 NM_012469.3 ?/. - c.2743G>A r.(?) p.(Val915Met)


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