Variant #0000524881 (NC_000005.9:g.149497358C>T, NM_002609.3:c.2960G>A (PDGFRB))

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.149497358C>T
DNA change (hg38) g.150117795C>T
Published as PDGFRB(NM_002609.3):c.2960G>A (p.R987Q)
ISCN -
DB-ID CSF1R_000068
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) 0.00027 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +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.2960G>A r.(?) p.(Arg987Gln)
CSF1R NM_005211.3 ?/. - c.-4715G>A r.(?) p.(=)


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