Product Details

SNP ID

rs141319322

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.10:123137124 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGCACAGACCGCGACTCTCCGGAGC[A/C]ACTGCTCAAGGCCGACCCCGATCAC

Phenotype

MIM: 600647 MIM: 613380

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

HMX2 PubMed Links

Gene Details

Gene

HMX2

Gene Name

H6 family homeobox 2

There are no transcripts associated with this gene.

Gene

HMX3

Gene Name

H6 family homeobox 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001105574.1	467	Missense Mutation	CAA,CCA	Q156P	NP_001099044.1

View Full Product Details