Variant #0000316595 (NC_000016.9:g.67876851_67876853del, NC_000016.9(NM_025082.3):c.-492+4478_-492+4480del (CENPT))

Chromosome 16
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.67876851_67876853del
DNA change (hg38) g.67842948_67842950del
Published as THAP11(NM_020457.2):c.394_396delCAG (p.Q132del)
ISCN -
DB-ID CENPT_000002
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NUTF2 NM_005796.1 -/. - c.-4067_-4065del r.(?) p.(=)
THAP11 NM_020457.2 -/. - c.394_396del r.(?) p.(Gln132del)
CENPT NM_025082.3 -/. - c.-492+4478_-492+4480del r.(=) p.(=)


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