Product Details

SNP ID
rs143268010
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.16:668562 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGAAGGTGCCCACCCACATCGTGGA[C/T]TACTCAGGTAGCGGCCGTAGCCTCC
Phenotype
MIM: 603264 MIM: 613889
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
LOC105371184 PubMed Links

Gene Details

Gene
LOC105371184
Gene Name
uncharacterized LOC105371184
There are no transcripts associated with this gene.

Gene
RHBDL1
Gene Name
rhomboid like 1
There are no transcripts associated with this gene.

Gene
RHOT2
Gene Name
ras homolog family member T2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_138769.2 288 Silent Mutation GAC,GAT D57D NP_620124.1
XM_005255660.2 288 Missense Mutation GAC,GAT D57D XP_005255717.1
XM_005255661.2 288 Missense Mutation GAC,GAT D57D XP_005255718.1
XM_005255662.2 288 Missense Mutation GAC,GAT D57D XP_005255719.1
XM_005255663.2 288 Missense Mutation GAC,GAT D57D XP_005255720.1
XM_006720970.2 288 UTR 5 XP_006721033.1
XM_006720973.2 288 UTR 5 XP_006721036.1
XM_017023825.1 288 Missense Mutation GAC,GAT D57D XP_016879314.1
XM_017023826.1 288 Missense Mutation GAC,GAT D57D XP_016879315.1
XM_017023827.1 288 Missense Mutation GAC,GAT D57D XP_016879316.1
XM_017023828.1 288 Missense Mutation GAC,GAT D57D XP_016879317.1
XM_017023829.1 288 Missense Mutation GAC,GAT D57D XP_016879318.1
XM_017023830.1 288 Silent Mutation GAC,GAT D57D XP_016879319.1
XM_017023831.1 288 UTR 5 XP_016879320.1
XM_017023832.1 288 UTR 5 XP_016879321.1
XM_017023833.1 288 UTR 5 XP_016879322.1
XM_017023834.1 288 UTR 5 XP_016879323.1
XM_017023835.1 288 UTR 5 XP_016879324.1
XM_017023836.1 288 UTR 5 XP_016879325.1
XM_017023837.1 288 UTR 5 XP_016879326.1
XM_017023838.1 288 UTR 5 XP_016879327.1
XM_017023839.1 288 UTR 5 XP_016879328.1
XM_017023840.1 288 UTR 5 XP_016879329.1
XM_017023841.1 288 UTR 5 XP_016879330.1
XM_017023842.1 288 UTR 5 XP_016879331.1
Gene
WDR90
Gene Name
WD repeat domain 90
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_145294.4 288 Intron NP_660337.3
XM_017023023.1 288 Intron XP_016878512.1
XM_017023024.1 288 Intron XP_016878513.1

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