Product Details

SNP ID

rs142468594

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.22:37912423 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCCCAATGACATGGTCTCCATGAGC[A/G]TCCCTGACTGCCTCAGCATCATGAC

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

MICALL1 PubMed Links

Gene Details

Gene

MICALL1

Gene Name

MICAL like 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_033386.3	356	Missense Mutation	ATC,GTC	I90V	NP_203744.1
XM_005261791.3	356	Missense Mutation	ATC,GTC	I90V	XP_005261848.1
XM_005261792.3	356	Missense Mutation	ATC,GTC	I90V	XP_005261849.1
XM_011530471.2	356	Missense Mutation	ATC,GTC	I90V	XP_011528773.1
XM_011530472.2	356	Missense Mutation	ATC,GTC	I90V	XP_011528774.1
XM_011530473.2	356	Missense Mutation	ATC,GTC	I90V	XP_011528775.1
XM_011530474.2	356	Missense Mutation	ATC,GTC	I6V	XP_011528776.1
XM_011530475.2	356	UTR 5			XP_011528777.1
XM_011530476.2	356	Missense Mutation	ATC,GTC	I90V	XP_011528778.1
XM_017029026.1	356	Intron			XP_016884515.1

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