Variant #0000886684 (NC_000005.9:g.149433689G>A, NM_005211.3:c.2862C>T (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.149433689G>A
DNA change (hg38) -
Published as CSF1R(NM_001288705.2):c.2862C>T (p.(Cys954=))
ISCN -
DB-ID HMGXB3_000023
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) 0.00044 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 2022-11-01 13:01:21 +01:00 (CET)
Date last edited 2024-02-26 20:06:56 +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.2862C>T r.(?) p.(Cys954=)
HMGXB3 NM_014983.2 -?/. - c.*1934G>A r.(=) p.(=)
TIGD6 NM_030953.3 -?/. - c.-53734C>T r.(?) p.(=)


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