Variant #0000720275 (NC_000005.9:g.149495377C>T, NM_002609.3:c.3270G>A (PDGFRB))

Chromosome 5
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.149495377C>T
DNA change (hg38) -
Published as PDGFRB(NM_001355017.1):c.2787G>A (p.P929=)
ISCN -
DB-ID CSF1R_000080
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) 0.00023 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 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     
PDGFRB NM_002609.3 -?/. - c.3270G>A r.(?) p.(Pro1090=)
CSF1R NM_005211.3 -?/. - c.-2734G>A r.(?) p.(=)


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