Variant #0000323510 (NC_000013.10:g.110866109T>A, NC_000013.10(NM_001845.4):c.279+20A>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.110866109T>A
DNA change (hg38) g.110213762T>A
Published as COL4A1(NM_001303110.1):c.279+20A>T (p.(=)), COL4A1(NM_001845.5):c.279+20A>T
ISCN -
DB-ID COL4A1_000158 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) 0.0026 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COL4A1 NM_001845.4 -?/. - c.279+20A>T r.(=) p.(=)


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