Product Details

SNP ID

rs1332607

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:35180771 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CTTTTGTTCATTAGTTCTGAAATCA[A/G]TTAAGTGGGTGACCAGCGTTAGGGG

Phenotype

MIM: 605836

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

UNC13B PubMed Links

Gene Details

Gene

UNC13B

Gene Name

unc-13 homolog B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_006377.3		Intron			NP_006368.3
XM_011517681.2		Intron			XP_011515983.1
XM_011517682.2		Intron			XP_011515984.1
XM_011517683.2		Intron			XP_011515985.1
XM_011517684.2		Intron			XP_011515986.1
XM_011517685.2		Intron			XP_011515987.1
XM_011517686.2		Intron			XP_011515988.1
XM_017014191.1		Intron			XP_016869680.1
XM_017014192.1		Intron			XP_016869681.1

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