Variant #0001068026 (NC_000013.10:g.110864215C>T, NC_000013.10(NM_001845.4):c.441+1G>A (COL4A1))

Chromosome 13
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.110864215C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID COL4A1_000359
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1445318211
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2026-02-02 11:51:01 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COL4A1 NM_001845.4 ?/. - c.441+1G>A r.(?) p.(?)


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