Variant #0000871769 (NC_000021.8:g.37833911G>A, NM_001146077.1:c.83C>T (CLDN14))

Chromosome 21
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.37833911G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID CLDN14_000020
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs727504989
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 2022-07-06 16:06:01 +02:00 (CEST)
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     
CLDN14 NM_001146077.1 ?/. - c.83C>T r.(?) p.(Pro28Leu)


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