Variant #0001047470 (NC_000013.10:g.110866346G>A, NM_001845.4:c.161C>T (COL4A1))

Chromosome 13
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.110866346G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID COL4A1_000055 See all 5 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs34004222
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00292 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-08-21 01:05:01 +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     
COL4A1 NM_001845.4 +?/. - c.161C>T r.(?) p.(Pro54Leu)


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