Product Details

SNP ID

rs2297775

Assay Type

Functionally tested

NCBI dbSNP Submissions

65

Location

Chr.1:155765221 on Build GRCh38

Set Membership

HapMap JSNP

Context Sequence [VIC/FAM]

CTACTAAGCCTCACTTCAGGATCCA[C/T]TGAGGACAAAGCATTCTTTGATGAT

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	4391	Missense Mutation	ATG,GTG	M1418V	NP_001269785.1
NM_001282858.1	4391	Missense Mutation	ATG,GTG	M1418V	NP_001269787.1
NM_001282860.1	4391	Missense Mutation	ATG,GTG	M1418V	NP_001269789.1
NM_001282861.1	4391	Missense Mutation	ATG,GTG	M1418V	NP_001269790.1
NM_032292.5	4391	Missense Mutation	ATG,GTG	M1418V	NP_115668.4
XM_005245284.3	4391	Missense Mutation	ATG,GTG	M1246V	XP_005245341.1
XM_005245286.3	4391	Missense Mutation	ATG,GTG	M614V	XP_005245343.1
XM_006711393.3	4391	Missense Mutation	ATG,GTG	M1418V	XP_006711456.1
XM_006711394.3	4391	Missense Mutation	ATG,GTG	M1418V	XP_006711457.1
XM_011509658.2	4391	Missense Mutation	ATG,GTG	M1389V	XP_011507960.1
XM_011509659.2	4391	Missense Mutation	ATG,GTG	M1246V	XP_011507961.1

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