Variant #0000689732 (NC_000006.11:g.41126619G>A, NM_018965.2:c.668C>T (TREM2))

Chromosome 6
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.41126619G>A
DNA change (hg38) -
Published as TREM2(NM_018965.2):c.668C>T (p.(Thr223Ile)), TREM2(NM_018965.3):c.668C>T (p.T223I), TREM2(NM_018965.4):c.668C>T (p.T223I)
ISCN -
DB-ID TREM2_000023 See all 3 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) 0.00082 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 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TREM2 NM_018965.2 -?/. - c.668C>T r.(?) p.(Thr223Ile)
TREML1 NM_178174.2 -?/. - c.-4593C>T r.(?) p.(=)


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