Product Details

SNP ID

rs61730956

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.13:100606369 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AACATTTTTCTTACCCAAATTACCA[C/T]GGTAACTTGCAGCATTTGGATTTGC

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

TMTC4 PubMed Links

Gene Details

Gene

TMTC4

Gene Name

transmembrane and tetratricopeptide repeat containing 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001079669.2	2379	Missense Mutation	CAT,CGT	H689R	NP_001073137.1
NM_001286453.1	2379	Missense Mutation	CAT,CGT	H578R	NP_001273382.1
NM_032813.3	2379	Missense Mutation	CAT,CGT	H708R	NP_116202.2
XM_011521121.2	2379	Missense Mutation	CAT,CGT	H766R	XP_011519423.1
XM_011521122.2	2379	Missense Mutation	CAT,CGT	H766R	XP_011519424.1
XM_011521123.2	2379	Missense Mutation	CAT,CGT	H747R	XP_011519425.1
XM_011521124.2	2379	Missense Mutation	CAT,CGT	H747R	XP_011519426.1
XM_011521125.1	2379	Intron			XP_011519427.1
XM_017020796.1	2379	Missense Mutation	CAT,CGT	H689R	XP_016876285.1
XM_017020797.1	2379	Missense Mutation	CAT,CGT	H530R	XP_016876286.1
XM_017020798.1	2379	Missense Mutation	CAT,CGT	H472R	XP_016876287.1
XM_017020799.1	2379	Missense Mutation	CAT,CGT	H472R	XP_016876288.1
XM_017020800.1	2379	Intron			XP_016876289.1

View Full Product Details