Product Details

SNP ID
rs200650722
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.16:668523 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCGCGGAGGAGATCACCATCCCCGC[G/T]GACGTCACCCCGGAGAAGGTGCCCA
Phenotype
MIM: 603264 MIM: 613889
Polymorphism
G/T, Transversion 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_138769.2 249 Silent Mutation GCG,GCT A44A NP_620124.1
XM_005255660.2 249 Silent Mutation GCG,GCT A44A XP_005255717.1
XM_005255661.2 249 Silent Mutation GCG,GCT A44A XP_005255718.1
XM_005255662.2 249 Silent Mutation GCG,GCT A44A XP_005255719.1
XM_005255663.2 249 Silent Mutation GCG,GCT A44A XP_005255720.1
XM_006720970.2 249 UTR 5 XP_006721033.1
XM_006720973.2 249 UTR 5 XP_006721036.1
XM_017023825.1 249 Silent Mutation GCG,GCT A44A XP_016879314.1
XM_017023826.1 249 Silent Mutation GCG,GCT A44A XP_016879315.1
XM_017023827.1 249 Silent Mutation GCG,GCT A44A XP_016879316.1
XM_017023828.1 249 Silent Mutation GCG,GCT A44A XP_016879317.1
XM_017023829.1 249 Silent Mutation GCG,GCT A44A XP_016879318.1
XM_017023830.1 249 Silent Mutation GCG,GCT A44A XP_016879319.1
XM_017023831.1 249 UTR 5 XP_016879320.1
XM_017023832.1 249 UTR 5 XP_016879321.1
XM_017023833.1 249 UTR 5 XP_016879322.1
XM_017023834.1 249 UTR 5 XP_016879323.1
XM_017023835.1 249 UTR 5 XP_016879324.1
XM_017023836.1 249 UTR 5 XP_016879325.1
XM_017023837.1 249 UTR 5 XP_016879326.1
XM_017023838.1 249 UTR 5 XP_016879327.1
XM_017023839.1 249 UTR 5 XP_016879328.1
XM_017023840.1 249 UTR 5 XP_016879329.1
XM_017023841.1 249 UTR 5 XP_016879330.1
XM_017023842.1 249 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_145294.4 249 Intron NP_660337.3
XM_017023023.1 249 Intron XP_016878512.1
XM_017023024.1 249 Intron XP_016878513.1

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