Variant #0000977205 (NC_000006.11:g.33380058dup, NM_015921.2:c.*4370dup (CUTA))

Chromosome 6
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.33380058dup
DNA change (hg38) -
Published as PHF1(NM_002636.5):c.18dupG (p.L7Afs*37)
ISCN -
DB-ID CUTA_000009
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2024-04-19 20:27:30 +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     
KIFC1 NM_002263.3 ?/. - c.*2591dup r.(?) p.(=)
PHF1 NM_002636.4 ?/. - c.18dup r.(?) p.(Leu7Alafs*37)
CUTA NM_015921.2 ?/. - c.*4370dup r.(?) p.(=)


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