Variant #0000980559 (NC_000013.10:g.110861757G>A, NM_001845.4:c.633C>T (COL4A1))

Chromosome 13
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.110861757G>A
DNA change (hg38) -
Published as COL4A1(NM_001845.5):c.633C>T (p.P211=), COL4A1(NM_001845.6):c.633C>T (p.P211=)
ISCN -
DB-ID COL4A1_000241 See all 2 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) 0.00024 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2024-04-19 20:27:30 +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.633C>T r.(?) p.(Pro211=)


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