Variant #0000524874 (NC_000005.9:g.149497177T>C, NC_000005.9(NM_002609.3):c.3137+4A>G (PDGFRB))

Chromosome 5
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.149497177T>C
DNA change (hg38) g.150117614T>C
Published as PDGFRB(NM_002609.3):c.3137+4A>G, PDGFRB(NM_002609.4):c.3137+4A>G
ISCN -
DB-ID PDGFRB_000015 See all 4 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) 0.34767 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PDGFRB NM_002609.3 -/. - c.3137+4A>G r.spl? p.?
CSF1R NM_005211.3 -/. - c.-4534A>G r.(?) p.(=)


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