Variant #0000524860 (NC_000005.9:g.149459839G>C, NM_005211.3:c.368C>G (CSF1R))

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.149459839G>C
DNA change (hg38) g.150080276G>C
Published as CSF1R(NM_001288705.2):c.368C>G (p.(Ala123Gly)), CSF1R(NM_005211.3):c.368C>G (p.A123G), CSF1R(NM_005211.4):c.368C>G (p.A123G)
ISCN -
DB-ID CSF1R_000057 See all 3 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) 0.00087 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 2023-07-07 10:10:56 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CSF1R NM_005211.3 -?/. - c.368C>G r.(?) p.(Ala123Gly)


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