Variant #0000266970 (NC_000013.10:g.111156499C>T, NM_001846.2:c.4290= (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.111156499C>T
DNA change (hg38) g.110504152C>T
Published as COL4A2(NM_001846.3):c.4290C>T (p.F1430=), COL4A2(NM_001846.4):c.4290C>T (p.F1430=), COL4A2-AS1(NR_046583.1):n.187-1224G>A
ISCN -
DB-ID COL4A2_000096 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) 0.98584 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COL4A2 NM_001846.2 -/. - c.4290= r.(=) p.(Phe1430=)
COL4A2-AS1 NR_046583.1 -/. - n.187-1224G>A r.(?) -


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.