Variant #0000929424 (NC_000008.10:g.145625538_145625539insGG, NC_000008.10(NM_013291.2):c.937+21_937+22insCC (CPSF1))

Chromosome 8
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.145625538_145625539insGG
DNA change (hg38) -
Published as CPSF1(NM_013291.3):c.937+21_937+22insCC
ISCN -
DB-ID CPSF1_000052
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2023-07-07 10:10:56 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CPSF1 NM_013291.2 -?/. - c.937+21_937+22insCC r.(=) p.(=)
MIR1234 NR_031600.1 -?/. - n.21_22insCC r.(?) -


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