Variant #0000925724 (NC_000013.10:g.110863985_110863989del, NC_000013.10(NM_001845.4):c.468+15_468+19del (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.110863985_110863989del
DNA change (hg38) -
Published as COL4A1(NM_001845.4):c.468+15_468+19del (p.(=)), COL4A1(NM_001845.5):c.468+15_468+19delATTTT, COL4A1(NM_001845.6):c.468+15_468+19delATTTT
ISCN -
DB-ID COL4A1_000065 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) 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 2023-04-16 21:50:28 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COL4A1 NM_001845.4 -/. - c.468+15_468+19del r.(=) p.(=)


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