Variant #0000307094 (NC_000017.10:g.1552537G>C, NM_006445.3:c.*1559C>G (PRPF8))

Chromosome 17
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.1552537G>C
DNA change (hg38) g.1649243G>C
Published as RILP(NM_031430.2):c.386C>G (p.A129G)
ISCN -
DB-ID RILP_000001
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_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 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SCARF1 NM_003693.2 ?/. - c.-3546C>G r.(?) p.(=)
PRPF8 NM_006445.3 ?/. - c.*1559C>G r.(=) p.(=)
RILP NM_031430.2 ?/. - c.386C>G r.(?) p.(Ala129Gly)


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