Variant #0000831176 (NC_000016.9:g.88871004C>T, NM_030928.3:c.280C>T (CDT1))

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.88871004C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID CDT1_000029
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs757078098
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2021-12-27 15:32:01 +01:00 (CET)
Date last edited 2022-09-26 12:22:42 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CDT1 NM_030928.3 ?/. - c.280C>T r.(?) p.(Pro94Ser)


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