Variant #0000686929 (NC_000006.11:g.137143922A>G, PEX7(NM_000288.3):c.119A>G)

Individual ID 00310245
Chromosome 6
Allele Parent #2
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.137143922A>G
DNA change (hg38) -
Published as [119G>A;340-10A>G]
ISCN -
DB-ID PEX7_000041
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) 4.0E-5 View details
Owner Nancy Braverman
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PEX7 NM_000288.3 ?/. - c.119A>G r.(?) p.(Tyr40Cys)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000311394 DNA SEQ - - PEX7 3 Nancy Braverman