Variant #0000859820 (NC_000005.9:g.149435669T>C, NM_005211.3:c.2474A>G (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.149435669T>C
DNA change (hg38) -
Published as CSF1R(NM_001349736.1):c.2474A>G (p.E825G)
ISCN -
DB-ID HMGXB3_000021
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:51:19 +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.2474A>G r.(?) p.(Glu825Gly)
HMGXB3 NM_014983.2 ?/. - c.*3914T>C r.(=) p.(=)
TIGD6 NM_030953.3 ?/. - c.-55714A>G r.(?) p.(=)


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