Variant #0000526016 (NC_000005.9:g.74670041del, NC_000005.9(NM_001130105.1):c.*10-8del (COL4A3BP))

Chromosome 5
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.74670041del
DNA change (hg38) g.75374216del
Published as COL4A3BP(NM_001130105.1):c.*10-8del (p.(=)), COL4A3BP(NM_001130105.1):c.*10-8delT
ISCN -
DB-ID COL4A3BP_000013 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2019-12-04 15:24:38 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COL4A3BP NM_001130105.1 -?/. - c.*10-8del r.(=) p.(=)
POLK NM_016218.2 -?/. - c.-137712del r.(?) p.(=)


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