Variant #0000923690 (NC_000002.11:g.37475273T>C, NC_000002.11(NM_144736.4):c.1111-5T>C (NDUFAF7))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.37475273T>C
DNA change (hg38) -
Published as NDUFAF7(NM_144736.5):c.1111-5T>C
ISCN -
DB-ID PRKD3_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) 0.00219 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-04-16 21:50:28 +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     
PRKD3 NM_005813.3 -?/. - c.*5047A>G r.(=) p.(=)
NDUFAF7 NM_144736.4 -?/. - c.1111-5T>C r.spl? p.?


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