Variant #0000995165 (NC_000005.9:g.74681777T>C, NM_001130105.1:c.1751A>G (COL4A3BP))

Chromosome 5
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.74681777T>C
DNA change (hg38) -
Published as COL4A3BP(NM_001130105.1):c.1751A>G (p.(His584Arg))
ISCN -
DB-ID POLK_000010
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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COL4A3BP NM_001130105.1 ?/. - c.1751A>G r.(?) p.(His584Arg)
POLK NM_016218.2 ?/. - c.-125976T>C r.(?) p.(=)


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