View genomic variant #0000003445

Chromosome X
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Type ins
DNA change (genomic) (Relative to hg19 / GRCh37) g.100600984_100600985insTCA
Published as -
GERP -
Segregation -
DB-ID TIMM8A_000006
MSCV MSCV_0003445
dbSNP ID -
Frequency -
Sources ;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) Variant not found in online data sets
Owner LOVD




Variant on transcripts

3 entries on 1 page. Showing entries 1 - 3.
Legend  

Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
TIMM8A 00000328 NM_001145951.1 0000003445 ?/? - - c.*2390_*2391insTGA p.(=) - - - -
TIMM8A 00000327 NM_004085.3 0000003445 ?/? - - c.*502_*503insTGA p.(=) - - - -
TIMM8A 00000326 XM_005262092.1 0000003445 ?/? - - c.132+2536_132+2537insTGA p.(=) - - - -
Legend  


MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

None

Ensembl Variant Phenotype Information:

None