Variant #0000609573 (NC_000005.9:g.149433902C>T, NM_005211.3:c.2746G>A (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.149433902C>T
DNA change (hg38) g.150054339C>T
Published as CSF1R(NM_001349736.1):c.2746G>A (p.E916K), CSF1R(NM_005211.4):c.2746G>A (p.E916K)
ISCN -
DB-ID HMGXB3_000012 See all 2 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) 0.00034 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 2019-12-04 15:24:38 +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     
CSF1R NM_005211.3 -?/. - c.2746G>A r.(?) p.(Glu916Lys)
HMGXB3 NM_014983.2 -?/. - c.*2147C>T r.(=) p.(=)
TIGD6 NM_030953.3 -?/. - c.-53947G>A r.(?) p.(=)


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