Variant #0001007086 (NC_000013.10:g.111082300T>A, NM_001846.2:c.546T>A (COL4A2))

Chromosome 13
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.111082300T>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID COL4A2_000232
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs535492357
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 2.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2024-09-05 10:19:01 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COL4A2 NM_001846.2 +/. - c.546T>A r.(?) p.(Tyr182Ter)


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