View genomic variant #0000001041

Chromosome 5
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Does not affect function
Type subst
DNA change (genomic) (Relative to hg19 / GRCh37) g.131705627C>A
Published as -
GERP -0.801
Segregation -
DB-ID SLC22A5_000051
MSCV MSCV_0001041
dbSNP ID rs1045018
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

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     
SLC22A5 00001145 NM_003060.3 0000001041 -/- - - c.-38C>A p.(=) - - - -
SLC22A5 00001144 XM_005272055.1 0000001041 -/- - - c.-38C>A p.(=) - - - -
SLC22A5 00001146 XM_005272056.1 0000001041 -/- - - c.-438C>A p.(=) - - - -
Legend  


MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

None

Ensembl Variant Phenotype Information:

None