Variant #0000724357 (NC_000013.10:g.111160444A>G, NM_001846.2:c.4757A>G (COL4A2))

Chromosome 13
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.111160444A>G
DNA change (hg38) -
Published as COL4A2(NM_001846.4):c.4757A>G (p.Y1586C)
ISCN -
DB-ID COL4A2_000105
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) Retrieve
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COL4A2 NM_001846.2 ?/. - c.4757A>G r.(?) p.(Tyr1586Cys)
COL4A2-AS1 NR_046583.1 ?/. - n.81+2T>C r.(?) -


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