Variant #0000331017 (NC_000006.11:g.41129252C>T, NM_018965.2:c.140G>A (TREM2))

Chromosome 6
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.41129252C>T
DNA change (hg38) g.41161514C>T
Published as TREM2(NM_001271821.1):c.140G>A (p.(Arg47His)), TREM2(NM_018965.3):c.140G>A (p.R47H), TREM2(NM_018965.4):c.140G>A (p.R47H)
ISCN -
DB-ID TREM2_000020 See all 4 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) 0.0026 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 2018-01-15 20:58:59 +01:00 (CET)
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     
TREM2 NM_018965.2 ?/. - c.140G>A r.(?) p.(Arg47His)


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