Product Details

SNP ID

rs16837037

Assay Type

Functionally tested

NCBI dbSNP Submissions

41

Location

Chr.1:155756499 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TCAGCCTGACCTTTGGTTTGTTCTC[C/T]GTGATCGTCTCAGATCCTAGAGCCT

Phenotype

MIM: 610393

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

GON4L PubMed Links

Gene Details

Gene

GON4L

Gene Name

gon-4 like

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001282856.1		Intron			NP_001269785.1
NM_001282858.1		Intron			NP_001269787.1
NM_001282860.1		Intron			NP_001269789.1
NM_001282861.1		Intron			NP_001269790.1
NM_032292.5		Intron			NP_115668.4
XM_005245284.3		Intron			XP_005245341.1
XM_005245286.3		Intron			XP_005245343.1
XM_006711393.3		Intron			XP_006711456.1
XM_006711394.3		Intron			XP_006711457.1
XM_011509658.2		Intron			XP_011507960.1
XM_011509659.2		Intron			XP_011507961.1

Gene

MSTO2P

Gene Name

misato family member 2, pseudogene

There are no transcripts associated with this gene.

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