Variant #0000863199 (NC_000013.10:g.111077229G>T, NC_000013.10(NM_001846.2):c.315+14G>T (COL4A2))

Chromosome 13
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.111077229G>T
DNA change (hg38) -
Published as COL4A2(NM_001846.2):c.315+14G>T (p.(=)), COL4A2(NM_001846.3):c.315+14G>T
ISCN -
DB-ID COL4A2_000008 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) 0.00534 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2022-05-09 15:51:19 +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.315+14G>T r.(=) p.(=)


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