Variant #0000320418 (NC_000001.10:g.1246390C>G, NM_001256456.1:c.*849G>C (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.1246390C>G
DNA change (hg38) g.1311010C>G
Published as PUSL1(NM_153339.1):c.801C>G (p.(His267Gln))
ISCN -
DB-ID PUSL1_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) 0.00908 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-07-07 10:10:56 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CPSF3L NM_001256456.1 ?/. - c.*849G>C r.(=) p.(=)
ACAP3 NM_030649.2 ?/. - c.-3195G>C r.(?) p.(=)
PUSL1 NM_153339.1 ?/. - c.801C>G r.(?) p.(His267Gln)


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