Variant #0000964141 (NC_000006.11:g.41126429C>T, NM_018965.2:c.*73G>A (TREM2))

Chromosome 6
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.41126429C>T
DNA change (hg38) -
Published as TREM2(NM_001271821.1):c.572G>A (p.(Trp191*)), TREM2(NM_001271821.2):c.572G>A (p.W191*)
ISCN -
DB-ID TREM2_000032 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) 0.00302 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2024-02-26 20:06:56 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TREM2 NM_018965.2 -/. - c.*73G>A r.(=) p.(=)
TREML1 NM_178174.2 -/. - c.-4403G>A r.(?) p.(=)


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