Product Details

SNP ID
rs201086643
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.16:668673 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCCCCTAGAAGCCGAGCAGACGGAC[A/G]AGGAGCTGCGGGAGGAGATCCACAA
Phenotype
MIM: 603264 MIM: 613889
Polymorphism
A/G, 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_138769.2 313 Missense Mutation AAG,GAG K66E NP_620124.1
XM_005255660.2 313 Missense Mutation AAG,GAG K66E XP_005255717.1
XM_005255661.2 313 Missense Mutation AAG,GAG K66E XP_005255718.1
XM_005255662.2 313 Missense Mutation AAG,GAG K66E XP_005255719.1
XM_005255663.2 313 Missense Mutation AAG,GAG K66E XP_005255720.1
XM_006720970.2 313 UTR 5 XP_006721033.1
XM_006720973.2 313 UTR 5 XP_006721036.1
XM_017023825.1 313 Missense Mutation AAG,GAG K66E XP_016879314.1
XM_017023826.1 313 Missense Mutation AAG,GAG K66E XP_016879315.1
XM_017023827.1 313 Missense Mutation AAG,GAG K66E XP_016879316.1
XM_017023828.1 313 Missense Mutation AAG,GAG K66E XP_016879317.1
XM_017023829.1 313 Missense Mutation AAG,GAG K66E XP_016879318.1
XM_017023830.1 313 Missense Mutation AAG,GAG K66E XP_016879319.1
XM_017023831.1 313 UTR 5 XP_016879320.1
XM_017023832.1 313 UTR 5 XP_016879321.1
XM_017023833.1 313 UTR 5 XP_016879322.1
XM_017023834.1 313 UTR 5 XP_016879323.1
XM_017023835.1 313 UTR 5 XP_016879324.1
XM_017023836.1 313 UTR 5 XP_016879325.1
XM_017023837.1 313 UTR 5 XP_016879326.1
XM_017023838.1 313 UTR 5 XP_016879327.1
XM_017023839.1 313 UTR 5 XP_016879328.1
XM_017023840.1 313 UTR 5 XP_016879329.1
XM_017023841.1 313 UTR 5 XP_016879330.1
XM_017023842.1 313 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_145294.4 313 Intron NP_660337.3
XM_017023023.1 313 Intron XP_016878512.1
XM_017023024.1 313 Intron XP_016878513.1

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