Variant #0000851846 (NC_000008.10:g.145622991_145622997del, NM_013291.2:c.2171_2177del (CPSF1))

Chromosome 8
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.145622991_145622997del
DNA change (hg38) -
Published as CPSF1(NM_013291.2):c.2171_2177del (p.(Arg724ProfsTer83)), CPSF1(NM_013291.3):c.2171_2177delGCAGTGG (p.R724Pfs*83)
ISCN -
DB-ID CPSF1_000003 See all 2 reported entries
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) 0.00025 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 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CPSF1 NM_013291.2 ?/. - c.2171_2177del r.(?) p.(Arg724ProfsTer83)
ADCK5 NM_174922.3 ?/. - c.*4702_*4708del r.(=) p.(=)


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