Variant #0000544667 (NC_000011.9:g.60230588C>A, NM_021950.3:c.273C>A (MS4A1))

Chromosome 11
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.60230588C>A
DNA change (hg38) g.60463115C>A
Published as MS4A1(NM_152866.2):c.273C>A (p.G91=), MS4A1(NM_152866.3):c.273C>A (p.G91=)
ISCN -
DB-ID MS4A1_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) Retrieve
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 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MS4A1 NM_021950.3 -?/. - c.273C>A r.(?) p.(Gly91=)


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