Variant #0000688156 (NC_000001.10:g.36933198G>A, NM_156039.3:c.1919C>T (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.36933198G>A
DNA change (hg38) -
Published as CSF3R(NM_000760.4):c.1919C>T (p.T640I), CSF3R(NM_156039.3):c.1919C>T (p.T640I)
ISCN -
DB-ID CSF3R_000023 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) 0.00042 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 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +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.-3322C>T r.(?) p.(=)
CSF3R NM_156039.3 -?/. - c.1919C>T r.(?) p.(Thr640Ile)


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