Product Details

SNP ID

rs7816792

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.8:97885233 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

TATACATTTTGAAACAAATAAGCCT[A/G]GACTTTTTATCTGCTCGGTTTGGAG

Phenotype

MIM: 602108

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

MATN2 PubMed Links

Gene Details

Gene

MATN2

Gene Name

matrilin 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001317748.1		Intron			NP_001304677.1
NM_002380.4		Intron			NP_002371.3
NM_030583.3		Intron			NP_085072.2
XM_005250920.1		Intron			XP_005250977.1
XM_017013417.1		Intron			XP_016868906.1
XM_017013418.1		Intron			XP_016868907.1

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