Variant #0001052158 (NC_000005.9:g.149495498T>C, NM_002609.3:c.3149A>G (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.149495498T>C
DNA change (hg38) -
Published as PDGFRB(NM_002609.4):c.3149A>G (p.(Asn1050Ser))
ISCN -
DB-ID CSF1R_000107
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +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.3149A>G r.(?) p.(Asn1050Ser)
CSF1R NM_005211.3 ?/. - c.-2855A>G r.(?) p.(=)


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