Variant #0000979793 (NC_000011.9:g.67804028G>A, NM_006019.3:c.-2563G>A (TCIRG1))

Chromosome 11
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.67804028G>A
DNA change (hg38) -
Published as NDUFS8(NM_002496.4):c.601G>A (p.(Ala201Thr))
ISCN -
DB-ID NDUFS8_000018
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) 4.0E-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     
NDUFS8 NM_002496.3 ?/. - c.601G>A r.(?) p.(Ala201Thr)
TCIRG1 NM_006019.3 ?/. - c.-2563G>A r.(?) p.(=)


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