Variant #0000536043 (NC_000009.11:g.116060212G>A, NM_004697.4:c.*6272G>A (PRPF4))

Chromosome 9
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.116060212G>A
DNA change (hg38) g.113297932G>A
Published as RNF183(NM_145051.3):c.253C>T (p.(Arg85Cys))
ISCN -
DB-ID PRPF4_000019
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) 0.00671 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PRPF4 NM_004697.4 -?/. - c.*6272G>A r.(=) p.(=)
RNF183 NM_145051.3 -?/. - c.253C>T r.(?) p.(Arg85Cys)


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