Variant #0000549794 (NC_000013.10:g.110960474A>G, NM_001845.4:c.-1100T>C (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.110960474A>G
DNA change (hg38) g.110308127A>G
Published as COL4A2(NM_001846.2):c.99+4A>G (p.?), COL4A2(NM_001846.3):c.99+4A>G, COL4A2(NM_001846.4):c.99+4A>G
ISCN -
DB-ID COL4A1_000203 See all 3 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) 0.00025 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +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.-1100T>C r.(?) p.(=)
COL4A2 NM_001846.2 -?/. - c.99+4A>G r.spl? p.?


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