Product Details

SNP ID

rs199720543

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.10:123137096 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTTGCTGAGAGACTCCTCCCCCGCC[G/T]CCGGCACAGACCGCGACTCTCCGGA

Phenotype

MIM: 600647 MIM: 613380

Polymorphism

G/T, 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	439	Missense Mutation	GCC,TCC	A147S	NP_001099044.1

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