RGD:152107775 Rat Genome Database

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Variant: RGD:152107775 -  Homo sapiens

RGD ID: 152107775
RS ID: rs1267157852
ClinVar ID: CV1529899
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TANGO2  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 22 20,040,949
GRCh38 22 20,053,426
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001322146.2:c.153C>G
NM_001322148.2:c.153C>G
NM_001322160.2:c.153C>G
NM_001283179.3:c.265+842C>G
More... 		06/01/2021 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:TANGO2
Accession:NM_001322146
Location:EXON
Amino Acid Prediction: P to P (synonymous)
Amino Acid Position: 51
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MAGHQHTWQAGSTHQLPAAAAGLAGPRARGPHISVPGRRAHACSCGHSICPLPTGELVTHFLTTDVDSLSYLKKVSMEGH
LYNGFNLIAADLSTAKGDVICYYGNRGEPDPIVLTPGTYGLSNALLETPWRKLCFGKQLFLEAVERSQALPKDVLIASLL
DVLNNEEAQLPDPAIEDQGGEYVQPMLSKYAAVCVRCPGYGTRYCSTVGAPPPIPCPTSHARGPAKKPSAHSQSQASSSP
EWIPELLPCPDAAAGTNTIILVDADGHVTFTERSMMDKDLSHWETRTYEFTLQS*

Gene Symbol:TANGO2
Accession:NM_001322160
Location:EXON
Amino Acid Prediction: P to P (synonymous)
Amino Acid Position: 51
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MAGHQHTWQAGSTHQLPAAAAGLAGPRARGPHISVPGRRAHACSCGHSICPLPTGELVTHFLTTDVDSLSYLKKVSMEGH
LYNGFNLIAADLSTAKGDVICYYGNRGEPDPIVLTPGTYGLSNALLETPWRKLCFGKQLFLEAVERSQALPKDVLIASLL
DVLNNEEAAARPGHRGPGWGVRAAHAEQVRGCVRALPWLRHQNQHYHPGRCGRPRDLH*

Gene Symbol:TANGO2
Accession:NM_001322148
Location:EXON
Amino Acid Prediction: P to P (synonymous)
Amino Acid Position: 51
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MAGHQHTWQAGSTHQLPAAAAGLAGPRARGPHISVPGRRAHACSCGHSICPLPTGELVTHFLTTDVDSLSYLKKVSMEGH
LYNGFNLIAADLSTAKGDVICYYGNRGEPDPIVLTPGTYGLSNALLETPWRKLCFGKQLFLEAVERSQALPKDVLIASLL
DVLNNEEAQLPDPAIEDQGGEYVQPMLSKYAAVCVRCPGYGTRTNTIILVDADGHVTFTERSMMDKDLSHWETRTYEFTL
QS*

Gene Symbol:TANGO2
Accession:NM_001322141
Location:INTRON

Gene Symbol:TANGO2
Accession:NM_001322173
Location:INTRON

Gene Symbol:TANGO2
Accession:XM_017028585
Location:INTRON

Gene Symbol:TANGO2
Accession:XM_047441124
Location:INTRON

Gene Symbol:TANGO2
Accession:XM_047441126
Location:INTRON

Gene Symbol:TANGO2
Accession:NM_001283148
Location:INTRON

Gene Symbol:TANGO2
Accession:XM_047441119
Location:INTRON

Gene Symbol:TANGO2
Accession:NM_001322144
Location:INTRON

Gene Symbol:TANGO2
Accession:NM_001322150
Location:INTRON

Gene Symbol:TANGO2
Accession:NM_001322169
Location:INTRON

Gene Symbol:TANGO2
Accession:NM_001322143
Location:INTRON

Gene Symbol:TANGO2
Accession:NM_001322171
Location:INTRON

Gene Symbol:TANGO2
Accession:XM_047441120
Location:INTRON

Gene Symbol:TANGO2
Accession:NM_001322166
Location:INTRON

Gene Symbol:TANGO2
Accession:XM_047441118
Location:INTRON

Gene Symbol:TANGO2
Accession:XM_047441132
Location:INTRON

Gene Symbol:TANGO2
Accession:NM_001283186
Location:INTRON

Gene Symbol:TANGO2
Accession:NM_001322175
Location:INTRON

Gene Symbol:TANGO2
Accession:XM_047441127
Location:INTRON

Gene Symbol:TANGO2
Accession:NM_001283235
Location:INTRON

Gene Symbol:TANGO2
Accession:XM_017028577
Location:INTRON

Gene Symbol:TANGO2
Accession:NM_001322142
Location:INTRON

Gene Symbol:TANGO2
Accession:XM_017028579
Location:INTRON

Gene Symbol:TANGO2
Accession:XM_047441131
Location:INTRON

Gene Symbol:TANGO2
Accession:XM_047441128
Location:INTRON

Gene Symbol:TANGO2
Accession:NM_001283116
Location:INTRON

Gene Symbol:TANGO2
Accession:NM_001283215
Location:INTRON

Gene Symbol:TANGO2
Accession:NM_001322149
Location:INTRON

Gene Symbol:TANGO2
Accession:NM_001322167
Location:INTRON

Gene Symbol:TANGO2
Accession:NM_001322145
Location:INTRON

Gene Symbol:TANGO2
Accession:XM_047441121
Location:INTRON

Gene Symbol:TANGO2
Accession:XM_047441129
Location:INTRON

Gene Symbol:TANGO2
Accession:NM_001283129
Location:INTRON

Gene Symbol:TANGO2
Accession:NM_001322172
Location:INTRON

Gene Symbol:TANGO2
Accession:NM_001322155
Location:INTRON

Gene Symbol:TANGO2
Accession:XM_017028580
Location:INTRON

Gene Symbol:TANGO2
Accession:NM_001322174
Location:INTRON

Gene Symbol:TANGO2
Accession:XM_017028586
Location:INTRON

Gene Symbol:TANGO2
Accession:XM_047441130
Location:INTRON

Gene Symbol:TANGO2
Accession:XM_047441122
Location:INTRON

Gene Symbol:TANGO2
Accession:NM_001283106
Location:INTRON

Gene Symbol:TANGO2
Accession:XM_047441123
Location:INTRON

Gene Symbol:TANGO2
Accession:XM_047441125
Location:INTRON

Gene Symbol:TANGO2
Accession:NM_001322163
Location:INTRON

Gene Symbol:TANGO2
Accession:NM_001322153
Location:INTRON

Gene Symbol:TANGO2
Accession:NM_001283154
Location:INTRON

Gene Symbol:TANGO2
Accession:NM_001283199
Location:INTRON

Gene Symbol:TANGO2
Accession:NM_001322147
Location:INTRON

Gene Symbol:TANGO2
Accession:NM_152906
Location:INTRON

Gene Symbol:TANGO2
Accession:NM_001283179
Location:INTRON

Gene Symbol:TANGO2
Accession:NM_001283248
Location:INTRON

Gene Symbol:TANGO2
Accession:NR_136206
Location:INTRON;NON-CODING

Gene Symbol:TANGO2
Accession:NR_136211
Location:INTRON;NON-CODING

Gene Symbol:TANGO2
Accession:NR_104275
Location:INTRON;NON-CODING

Gene Symbol:TANGO2
Accession:NR_136212
Location:INTRON;NON-CODING

Gene Symbol:TANGO2
Accession:NR_104274
Location:INTRON;NON-CODING

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002196380 CLINVAR
dbSNP (RS) rs1267157852 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene TANGO2 CLINVAR
OMIM 616830 CLINVAR