Variant #0000620377 (NC_000001.10:g.1247742G>A, NM_001256456.1:c.1489C>T (CPSF3L))

Chromosome 1
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.1247742G>A
DNA change (hg38) g.1312362G>A
Published as INTS11(NM_001256456.1):c.1489C>T (p.R497W)
ISCN -
DB-ID CPSF3L_000004
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 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2023-07-07 10:10:56 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CPSF3L NM_001256456.1 ?/. - c.1489C>T r.(?) p.(Arg497Trp)
ACAP3 NM_030649.2 ?/. - c.-4547C>T r.(?) p.(=)
PUSL1 NM_153339.1 ?/. - c.*983G>A r.(=) p.(=)


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