Product Details

SNP ID

rs148373816

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:47666995 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGTTTTCATTTTTCATTGGTAAAAA[A/G]CTGGAATTCTCTGAGTTTTTGAAAA

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

AGBL2 PubMed Links

Gene Details

Gene

AGBL2

Gene Name

ATP/GTP binding protein like 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_024783.3	2211	Silent Mutation	AGC,AGT	S803S	NP_079059.2
XM_005253138.4	2211	Silent Mutation	AGC,AGT	S765S	XP_005253195.1
XM_005253139.4	2211	Intron			XP_005253196.1
XM_005253140.4	2211	Intron			XP_005253197.1
XM_005253141.4	2211	Intron			XP_005253198.1
XM_006718327.3	2211	Silent Mutation	AGC,AGT	S747S	XP_006718390.1
XM_006718328.3	2211	Intron			XP_006718391.1
XM_011520372.2	2211	Silent Mutation	AGC,AGT	S765S	XP_011518674.1
XM_011520373.2	2211	Silent Mutation	AGC,AGT	S765S	XP_011518675.1
XM_011520374.2	2211	Silent Mutation	AGC,AGT	S729S	XP_011518676.1
XM_011520375.2	2211	Silent Mutation	AGC,AGT	S720S	XP_011518677.1
XM_011520376.2	2211	Silent Mutation	AGC,AGT	S667S	XP_011518678.1
XM_011520377.2	2211	Silent Mutation	AGC,AGT	S667S	XP_011518679.1
XM_011520378.2	2211	Silent Mutation	AGC,AGT	S667S	XP_011518680.1
XM_011520379.2	2211	Silent Mutation	AGC,AGT	S667S	XP_011518681.1
XM_011520381.2	2211	Intron			XP_011518683.1
XM_017018331.1	2211	Silent Mutation	AGC,AGT	S765S	XP_016873820.1
XM_017018332.1	2211	Silent Mutation	AGC,AGT	S727S	XP_016873821.1
XM_017018333.1	2211	Intron			XP_016873822.1

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