Variant #0000831400 (NC_000016.9:g.88872968C>T, NM_030928.3:c.1008C>T (CDT1))

Chromosome 16
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.88872968C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID CDT1_000030
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs778195622
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 3.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2021-12-29 12:02:01 +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.1008C>T r.(?) p.(Asn336=)


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