Product Details

SNP ID

rs140400255

Assay Type

Functionally tested

NCBI dbSNP Submissions

11

Location

Chr.1:230906915 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AATACAGCAGCAGAACTAGAGTTTC[G/T]TAAGACAACGTGGAGAAGAGTCTGT

Phenotype

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

TTC13 PubMed Links

Gene Details

Gene

TTC13

Gene Name

tetratricopeptide repeat domain 13

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001122835.2	3622	Missense Mutation	AAG,ACG	K804T	NP_001116307.2
NM_024525.4	3622	Missense Mutation	AAG,ACG	K858T	NP_078801.3
XM_005273260.1	3622	Missense Mutation	AAG,ACG	K857T	XP_005273317.1
XM_005273261.2	3622	Missense Mutation	AAG,ACG	K827T	XP_005273318.1
XM_005273262.1	3622	Missense Mutation	AAG,ACG	K805T	XP_005273319.1
XM_005273264.2	3622	Missense Mutation	AAG,ACG	K782T	XP_005273321.1
XM_006711814.2	3622	Missense Mutation	AAG,ACG	K779T	XP_006711877.1
XM_006711815.2	3622	Missense Mutation	AAG,ACG	K500T	XP_006711878.1
XM_011544275.2	3622	Missense Mutation	AAG,ACG	K751T	XP_011542577.1
XM_011544276.2	3622	Missense Mutation	AAG,ACG	K561T	XP_011542578.1
XM_017002321.1	3622	Missense Mutation	AAG,ACG	K826T	XP_016857810.1
XM_017002322.1	3622	Missense Mutation	AAG,ACG	K781T	XP_016857811.1
XM_017002323.1	3622	Missense Mutation	AAG,ACG	K729T	XP_016857812.1
XM_017002324.1	3622	Missense Mutation	AAG,ACG	K728T	XP_016857813.1
XM_017002325.1	3622	Missense Mutation	AAG,ACG	K499T	XP_016857814.1
XM_017002326.1	3622	Missense Mutation	AAG,ACG	K499T	XP_016857815.1

View Full Product Details