View genomic variant #0000000950

Chromosome 3
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Type ins
DNA change (genomic) (Relative to hg19 / GRCh37) g.128598494_128598495insTAAG
Published as -
GERP -
Segregation -
DB-ID ACAD9_000007
MSCV MSCV_0000950
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

2 entries on 1 page. Showing entries 1 - 2.
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Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Position     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
ACAD9 00000014 NM_014049.4 0000000950 ?/? - - c.-41_-40insTAAG - p.(=) - - - -
ACAD9 00000015 NR_033426.1 0000000950 ?/? - - n.162_163insTAAG - - - - - -
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MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

None

Ensembl Variant Phenotype Information:

None