Variant #0000657903 (NC_000016.9:g.67861397C>T, NM_025082.3:c.*773G>A (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.67861397C>T
DNA change (hg38) g.67827494C>T
Published as TSNAXIP1(NM_018430.3):c.1651C>T (p.P551S)
ISCN -
DB-ID CENPT_000004
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) 0.00082 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 2020-03-23 16:13:27 +01:00 (CET)
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.-19521C>T r.(?) p.(=)
TSNAXIP1 NM_018430.2 ?/. - c.1651C>T r.(?) p.(Pro551Ser)
THAP11 NM_020457.2 ?/. - c.-15061C>T r.(?) p.(=)
CENPT NM_025082.3 ?/. - c.*773G>A r.(=) p.(=)


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