Variant #0000864755 (NC_000016.9:g.3063631C>G, NM_020982.3:c.268C>G (CLDN9))

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.3063631C>G
DNA change (hg38) -
Published as CLDN9(NM_020982.4):c.268C>G (p.L90V)
ISCN -
DB-ID CLDN6_000003
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 16:01:56 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CLDN9 NM_020982.3 ?/. - c.268C>G r.(?) p.(Leu90Val)
CLDN6 NM_021195.4 ?/. - c.*1729G>C r.(=) p.(=)


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