Variant #0000973925 (NC_000001.10:g.36933759C>T, NM_156039.3:c.1640G>A (CSF3R))

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.36933759C>T
DNA change (hg38) -
Published as CSF3R(NM_000760.4):c.1640G>A (p.W547*)
ISCN -
DB-ID CSF3R_000044
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) 0.00025 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2024-04-19 20:20:39 +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     
MRPS15 NM_031280.3 +/. - c.-3883G>A r.(?) p.(=)
CSF3R NM_156039.3 +/. - c.1640G>A r.(?) p.(Trp547*)


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