Variant #0000976649 (NC_000005.9:g.149433973C>T, NM_005211.3:c.2675G>A (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.149433973C>T
DNA change (hg38) -
Published as CSF1R(NM_001288705.3):c.2675G>A (p.(Cys892Tyr))
ISCN -
DB-ID HMGXB3_000026
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CSF1R NM_005211.3 ?/. - c.2675G>A r.(?) p.(Cys892Tyr)
HMGXB3 NM_014983.2 ?/. - c.*2218C>T r.(=) p.(=)
TIGD6 NM_030953.3 ?/. - c.-54018G>A r.(?) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.