Variant #0000721528 (NC_000007.13:g.73245893C>G, NM_152559.2:c.*3180G>C (WBSCR27))

Chromosome 7
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.73245893C>G
DNA change (hg38) -
Published as CLDN4(NM_001305.5):c.362C>G (p.A121G)
ISCN -
DB-ID CLDN4_000002
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) 6.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CLDN4 NM_001305.3 ?/. - c.362C>G r.(?) p.(Ala121Gly)
WBSCR27 NM_152559.2 ?/. - c.*3180G>C r.(=) p.(=)


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