Product Details

SNP ID

rs4638862

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.20:45840651 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ACCCTCCCTGCAGCTCTACACCCTC[A/G]CCGTGATCGGCCCAGGACCGCCAGA

Phenotype

MIM: 608123 MIM: 191039

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

ACOT8 PubMed Links

Gene Details

Gene

ACOT8

Gene Name

acyl-CoA thioesterase 8

There are no transcripts associated with this gene.

Gene

SNX21

Gene Name

sorting nexin family member 21

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001042632.2	542	Silent Mutation	TCA,TCG	S151S	NP_001036097.1
NM_001042633.2	542	Silent Mutation	TCA,TCG	S157S	NP_001036098.1
NM_033421.3	542	Missense Mutation	ACC,GCC	T154A	NP_219489.1
NM_152897.2	542	Missense Mutation	ACC,GCC	T154A	NP_690857.1
XM_005260608.4	542	Missense Mutation	ACC,GCC	T56A	XP_005260665.1
XM_011529095.2	542	Missense Mutation	ACC,GCC	T6A	XP_011527397.1
XM_011529096.2	542	Intron			XP_011527398.1
XM_011529098.2	542	UTR 3			XP_011527400.1
XM_011529099.2	542	Intron			XP_011527401.1
XM_017028120.1	542	Intron			XP_016883609.1

Gene

TNNC2

Gene Name

troponin C2, fast skeletal type

There are no transcripts associated with this gene.

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