Variant #0001002489 (NC_000016.9:g.67862423C>G, NM_025082.3:c.1516G>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.67862423C>G
DNA change (hg38) -
Published as CENPT(NM_025082.3):c.1516G>C (p.(Gly506Arg))
ISCN -
DB-ID CENPT_000008
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) 2.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +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.-18495C>G r.(?) p.(=)
TSNAXIP1 NM_018430.2 ?/. - c.*527C>G r.(=) p.(=)
THAP11 NM_020457.2 ?/. - c.-14035C>G r.(?) p.(=)
CENPT NM_025082.3 ?/. - c.1516G>C r.(?) p.(Gly506Arg)


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