Variant #0000274178 (NC_000013.10:g.110960486C>T, NM_001845.4:c.-1112G>A (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.110960486C>T
DNA change (hg38) g.110308139C>T
Published as COL4A2(NM_001846.2):c.99+16C>T (p.(=)), COL4A2(NM_001846.3):c.99+16C>T
ISCN -
DB-ID COL4A2_000004 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) 0.00016 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2022-05-09 15:51:19 +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.-1112G>A r.(?) p.(=)
COL4A2 NM_001846.2 -?/. - c.99+16C>T r.(=) p.(=)


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