Variant #0001041263 (NC_000016.9:g.67862294C>G, NC_000016.9(NM_025082.3):c.1563-1G>C (CENPT))

Chromosome 16
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.67862294C>G
DNA change (hg38) -
Published as CENPT(NM_025082.4):c.1563-1G>C
ISCN -
DB-ID CENPT_000010
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +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     
NUTF2 NM_005796.1 ?/. - c.-18624C>G r.(?) p.(=)
TSNAXIP1 NM_018430.2 ?/. - c.*398C>G r.(=) p.(=)
THAP11 NM_020457.2 ?/. - c.-14164C>G r.(?) p.(=)
CENPT NM_025082.3 ?/. - c.1563-1G>C r.spl? p.?


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