Variant #0000507328 (NC_000001.10:g.36931985A>G, NM_156039.3:c.2565T>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.36931985A>G
DNA change (hg38) g.36466384A>G
Published as CSF3R(NM_156039.3):c.2565T>C (p.H855=)
ISCN -
DB-ID CSF3R_000007
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) 0.0002 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-08-06 14:59:34 +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.-2109T>C r.(?) p.(=)
CSF3R NM_156039.3 -?/. - c.2565T>C r.(?) p.(His855=)


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