Variant #0000330674 (NC_000005.9:g.149495360G>A, NM_002609.3:c.3287C>T (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.149495360G>A
DNA change (hg38) g.150115797G>A
Published as PDGFRB(NM_002609.3):c.3287C>T (p.A1096V, p.(Ala1096Val)), PDGFRB(NM_002609.4):c.3287C>T (p.A1096V)
ISCN -
DB-ID PDGFRB_000012 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) 0.00302 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 2018-01-15 20:58:59 +01:00 (CET)
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.3287C>T r.(?) p.(Ala1096Val)
CSF1R NM_005211.3 -?/. - c.-2717C>T r.(?) p.(=)


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