Product Details

SNP ID

rs115967744

Assay Type

Functionally tested

NCBI dbSNP Submissions

17

Location

Chr.1:185743476 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGCAGGTGATTTTGTTGGGGATTTA[A/G]ATGCAGTCTGGAATGTTTCAGCTGT

Phenotype

MIM: 608548

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

HMCN1 PubMed Links

Gene Details

Gene

HMCN1

Gene Name

hemicentin 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_031935.2		Intron			NP_114141.2
XM_011510038.2		Intron			XP_011508340.1
XM_011510041.2		Intron			XP_011508343.1
XM_017002437.1		Intron			XP_016857926.1

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