Variant #0000254740 (NC_000001.10:g.36932463A>G, NM_156039.3:c.2087T>C (CSF3R))

Chromosome 1
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.36932463A>G
DNA change (hg38) g.36466862A>G
Published as CSF3R(NM_156039.3):c.2087T>C (p.M696T, p.(Met696Thr))
ISCN -
DB-ID CSF3R_000002 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) 0.00623 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-08-28 13:07:21 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MRPS15 NM_031280.3 -?/. - c.-2587T>C r.(?) p.(=)
CSF3R NM_156039.3 -?/. - c.2087T>C r.(?) p.(Met696Thr)


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