Variant #0000549790 (NC_000013.10:g.110959356C>G, NM_001845.4:c.19G>C (COL4A1))

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.110959356C>G
DNA change (hg38) g.110307009C>G
Published as COL4A1(NM_001845.5):c.19G>C (p.V7L), COL4A1(NM_001845.6):c.19G>C (p.V7L)
ISCN -
DB-ID COL4A1_000052 See all 4 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) 0.43569 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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     
COL4A1 NM_001845.4 -/. - c.19G>C r.(?) p.(Val7Leu)
COL4A2 NM_001846.2 -/. - c.-564C>G r.(?) p.(=)


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