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SNP ID: rs17091403
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.10:114174146 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: AGACCGCGGTGAGAAACACAGCCGA[C/T]GCCTCACTCAGCGGCCGTTTCCCCA
Phenotype: MIM: 605796
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: CCDC186 PubMed Links

Gene Details

Gene: CCDC186
Gene Name: coiled-coil domain containing 186

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001321829.1	167	UTR 5			NP_001308758.1
NM_018017.3	167	UTR 5			NP_060487.2
NM_153249.1	167	UTR 5			NP_694981.1
XM_011539915.2	167	UTR 5			XP_011538217.1
XM_011539916.2	167	UTR 5			XP_011538218.1

Gene: MIR2110
Gene Name: microRNA 2110

There are no transcripts associated with this gene.

Gene: TDRD1
Gene Name: tudor domain containing 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_198795.1	167	Intron			NP_942090.1
XM_005269978.2	167	Intron			XP_005270035.1
XM_005269979.2	167	Intron			XP_005270036.1
XM_011539959.2	167	Intron			XP_011538261.1
XM_011539960.2	167	Intron			XP_011538262.1
XM_011539961.2	167	Intron			XP_011538263.1
XM_011539962.1	167	Intron			XP_011538264.1
XM_011539963.1	167	Intron			XP_011538265.1
XM_011539964.1	167	Intron			XP_011538266.1
XM_011539966.1	167	Intron			XP_011538268.1
XM_017016414.1	167	Intron			XP_016871903.1
XM_017016415.1	167	Intron			XP_016871904.1

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