Variant #0000605728 (NC_000001.10:g.36932474C>T, NM_156039.3:c.2076G>A (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.36932474C>T
DNA change (hg38) g.36466873C>T
Published as CSF3R(NM_156039.3):c.2076G>A (p.(=))
ISCN -
DB-ID CSF3R_000015
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) 0.00049 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-12-04 14:54:23 +01:00 (CET)
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.-2598G>A r.(?) p.(=)
CSF3R NM_156039.3 -?/. - c.2076G>A r.(?) p.(Gln692=)


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