Variant #0000689462 (NC_000005.9:g.149433682C>G, NM_005211.3:c.2869G>C (CSF1R))

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.149433682C>G
DNA change (hg38) -
Published as CSF1R(NM_001349736.1):c.2869G>C (p.G957R)
ISCN -
DB-ID HMGXB3_000017
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CSF1R NM_005211.3 ?/. - c.2869G>C r.(?) p.(Gly957Arg)
HMGXB3 NM_014983.2 ?/. - c.*1927C>G r.(=) p.(=)
TIGD6 NM_030953.3 ?/. - c.-53727G>C r.(?) p.(=)


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