View genomic variant #0000016587

Chromosome 11
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.68527116C>T
Published as -
GERP -
Segregation -
DB-ID CPT1A_000028 See all 2 reported entries
MSCV MSCV_0000326
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) Variant not found in online data sets
Owner LOVD




Variant on transcripts

5 entries on 1 page. Showing entries 1 - 5.
Legend  

Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
CPT1A 00000660 NM_001031847.2 0000016587 ./. - - c.2156G>A p.(Gly719Asp) - - - -
CPT1A 00000662 NM_001876.3 0000016587 ./. - - c.2156G>A p.(Gly719Asp) - - - -
CPT1A 00000664 XM_005273762.1 0000016587 ./. - - c.2252G>A p.(Gly751Asp) - - - -
CPT1A 00000661 XM_005273763.1 0000016587 ./. - - c.2252G>A p.(Gly751Asp) - - - -
CPT1A 00000663 XM_005273764.1 0000016587 ./. - - c.2156G>A p.(Gly719Asp) - - - -
Legend  


MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

None

Ensembl Variant Phenotype Information:

None