Variant #0001053111 (NC_000008.10:g.125562065C>G, NM_014751.4:c.*3168G>C (MTSS1))

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.125562065C>G
DNA change (hg38) -
Published as NDUFB9(NM_005005.3):c.472C>G (p.(Arg158Gly))
ISCN -
DB-ID MTSS1_000005
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) 0.00026 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 2025-11-01 13:22:20 +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     
NDUFB9 NM_005005.2 ?/. - c.472C>G r.(?) p.(Arg158Gly)
MTSS1 NM_014751.4 ?/. - c.*3168G>C r.(=) p.(=)


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