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SNP ID

rs115529610

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:73203602 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCTGTGAACTTGAGCTACACACTTC[A/G]CTCTGAGCCTGCGTGCATGCAATGC

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

NOTO PubMed Links

Gene Details

Gene

NOTO

Gene Name

notochord homeobox

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001134462.1		Intron			NP_001127934.1

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