View genomic variant #0000000950

Chromosome 3
Allele Unknown
Affects function (reported) Effect unknown
Affects function (concluded) Effect unknown
Type ins
DNA change (genomic) (Relative to hg19 / GRCh37) g.128598494_128598495insTAAG
Published as -
GERP -
Segregation -
DB-ID ACAD9_000007
dbSNP ID -
Frequency -
Sources ;
Reference -
Variant remarks -
Genetic origin -
Average frequency (large NGS studies) Variant not found in online data sets
Owner LOVD




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Position     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
ACAD9 NM_014049.4 ?/? - - c.-41_-40insTAAG - p.(=) - - - -
ACAD9 NR_033426.1 ?/? - - n.162_163insTAAG - - - - - -


MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

None

Ensembl Variant Phenotype Information:

None