Variant #0000945927 (NC_000008.10:g.104709427A>T, NM_001348484.2:c.410A>T (RIMS2))

Chromosome 8
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.104709427A>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID RIMS2_000021 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs769908030
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 9.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2023-11-21 16:19:01 +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     
RIMS2 NM_001348484.2 ?/. - c.410A>T r.(?) p.(Lys137Ile)


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