Variant #0000545419 (NC_000011.9:g.67803828C>G, NM_006019.3:c.-2763C>G (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.67803828C>G
DNA change (hg38) g.68036361C>G
Published as NDUFS8(NM_002496.4):c.481C>G (p.P161A)
ISCN -
DB-ID NDUFS8_000011
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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NDUFS8 NM_002496.3 ?/. - c.481C>G r.(?) p.(Pro161Ala)
TCIRG1 NM_006019.3 ?/. - c.-2763C>G r.(?) p.(=)


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