Variant #0000607688 (NC_000002.11:g.228029482_228029505del, NM_000092.4:c.-874_-851del (COL4A4))

Chromosome 2
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.228029482_228029505del
DNA change (hg38) g.227164766_227164789del
Published as -
ISCN -
DB-ID COL4A3_000003 See all 11 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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COL4A3 NM_000091.4 ?/. - c.40_63del r.(?) p.(Leu14_Leu21del)
COL4A4 NM_000092.4 ?/. - c.-874_-851del r.(?) p.(=)


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