Variant #0000253508 (NC_000020.10:g.62614448A>G, NM_012469.3:c.120A>G (PRPF6))

Chromosome 20
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.62614448A>G
DNA change (hg38) g.63983095A>G
Published as PRPF6(NM_012469.3):c.120A>G (p.A40=)
ISCN -
DB-ID PRPF6_000005
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) 0.00397 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 2020-07-16 21:53:32 +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.120A>G r.(?) p.(Ala40=)
SAMD10 NM_080621.4 -/. - c.-3628T>C r.(?) p.(=)


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