Variant #0000975052 (NC_000002.11:g.228029485_228029496del, NM_000092.4:c.-865_-854del (COL4A4))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.228029485_228029496del
DNA change (hg38) -
Published as COL4A3(NM_000091.5):c.43_54del (p.(Pro15_Leu18del))
ISCN -
DB-ID COL4A3_000460 See all 2 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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:20:39 +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     
COL4A3 NM_000091.4 -?/. - c.43_54del r.(?) p.(Pro15_Leu18del)
COL4A4 NM_000092.4 -?/. - c.-865_-854del r.(?) p.(=)


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