Variant #0000976762 (NC_000005.9:g.1801568C>A, NM_004553.4:c.37C>A (NDUFS6))

Chromosome 5
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.1801568C>A
DNA change (hg38) -
Published as NDUFS6(NM_004553.6):c.37C>A (p.(Arg13=))
ISCN -
DB-ID MRPL36_000002
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) 1.0E-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 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NDUFS6 NM_004553.4 ?/. - c.37C>A r.(?) p.(=)
MRPL36 NM_032479.3 ?/. - c.-1675G>T r.(?) p.(=)


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