Variant #0000851767 (NC_000008.10:g.104943552A>C, NM_001100117.2:c.2306A>C (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.104943552A>C
DNA change (hg38) -
Published as RIMS2(NM_001348484.1):c.2531A>C (p.D844A)
ISCN -
DB-ID RIMS2_000016
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) 0.00391 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 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RIMS2 NM_001100117.2 ?/. - c.2306A>C r.(?) p.(Asp769Ala)
RIMS2 NM_001348484.2 ?/. - c.2531A>C r.(?) p.(Asp844Ala)


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