Product Details

SNP ID

rs201226192

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:108381559 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGCAGGGGATGCTATTCTTCTTGAA[A/C]CTGAAAAACAGAATGTCAGTGTGTT

Phenotype

MIM: 604371 MIM: 609929

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

HHLA2 PubMed Links

Gene Details

Gene

HHLA2

Gene Name

HERV-H LTR-associating 2

There are no transcripts associated with this gene.

Gene

MYH15

Gene Name

myosin heavy chain 15

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_014981.1	6005	Missense Mutation			NP_055796.1
XM_011512559.2	6005	Missense Mutation			XP_011510861.1
XM_017005922.1	6005	Missense Mutation			XP_016861411.1

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