Variant #0000549788 (NC_000013.10:g.110866346G>A, NM_001845.4:c.161C>T (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.110866346G>A
DNA change (hg38) g.110213999G>A
Published as COL4A1(NM_001303110.1):c.161C>T (p.(Pro54Leu)), COL4A1(NM_001845.5):c.161C>T (p.P54L), COL4A1(NM_001845.6):c.161C>T (p.P54L)
ISCN -
DB-ID COL4A1_000055 See all 5 reported entries
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) 0.00292 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
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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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