Variant #0000913322 (NC_000010.10:g.74311075G>C, NM_001195518.2:c.355C>G (MICU1))

Chromosome 10
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.74311075G>C
DNA change (hg38) g.72551317G>C
Published as MICU1(NM_001195518.1):c.355C>G (p.(Arg119Gly))
ISCN -
DB-ID MICU1_000027
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID rs538329212
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 2.0E-5 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 2023-01-11 15:44:22 +01:00 (CET)
Date last edited 2025-09-08 12:54:02 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MICU1 NM_001195518.2 ?/. - c.355C>G r.(?) p.(Arg119Gly)


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