Variant #0000720492 (NC_000005.9:g.74712697T>C, NC_000005.9(NM_001130105.1):c.1221+4A>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.74712697T>C
DNA change (hg38) -
Published as CERT1(NM_005713.3):c.837+4A>G
ISCN -
DB-ID POLK_000005
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) 1.0E-5 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2021-02-08 18:36:18 +01:00 (CET)
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.1221+4A>G r.spl? p.?
POLK NM_016218.2 ?/. - c.-95056T>C r.(?) p.(=)


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