Variant #0000525870 (NC_000005.9:g.60448579C>T, NM_174889.4:c.307C>T (NDUFAF2))

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.60448579C>T
DNA change (hg38) g.61152752C>T
Published as NDUFAF2(NM_174889.4):c.307C>T (p.(Gln103Ter))
ISCN -
DB-ID NDUFAF2_000004
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-17 10:25:07 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SMIM15 NM_001048249.3 ?/. - c.*7195G>A r.(=) p.(=)
NDUFAF2 NM_174889.4 ?/. - c.307C>T r.(?) p.(Gln103Ter)


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