Variant #0000850961 (NC_000005.9:g.74706915_74706919del, NM_001130105.1:c.1236_1240del (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.74706915_74706919del
DNA change (hg38) -
Published as COL4A3BP(NM_001130105.1):c.1236_1240delAAGAA (p.R413Nfs*6)
ISCN -
DB-ID POLK_000008
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:40:45 +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     
COL4A3BP NM_001130105.1 ?/. - c.1236_1240del r.(?) p.(Arg413Asnfs*6)
POLK NM_016218.2 ?/. - c.-100838_-100834del r.(?) p.(=)


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