Product Details

SNP ID

rs3785888

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:46928337 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TGGCTGGCATTGGTAGATTTGGGGT[C/T]CTGGTTTGCATTGCTCACGATGCAG

Phenotype

MIM: 604027

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

GOSR2 PubMed Links

Gene Details

Gene

GOSR2

Gene Name

golgi SNAP receptor complex member 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001012511.2		Intron			NP_001012529.1
NM_001321133.1		Intron			NP_001308062.1
NM_001321134.1		Intron			NP_001308063.1
NM_004287.4		Intron			NP_004278.2
NM_054022.3		Intron			NP_473363.1
XM_005257844.3		Intron			XP_005257901.1
XM_006722190.3		Intron			XP_006722253.1
XM_011525501.2		Intron			XP_011523803.1
XM_011525502.2		Intron			XP_011523804.1
XM_017025378.1		Intron			XP_016880867.1
XM_017025379.1		Intron			XP_016880868.1
XM_017025380.1		Intron			XP_016880869.1
XM_017025381.1		Intron			XP_016880870.1
XM_017025382.1		Intron			XP_016880871.1
XM_017025383.1		Intron			XP_016880872.1
XM_017025384.1		Intron			XP_016880873.1
XM_017025385.1		Intron			XP_016880874.1
XM_017025386.1		Intron			XP_016880875.1
XM_017025387.1		Intron			XP_016880876.1
XM_017025388.1		Intron			XP_016880877.1
XM_017025389.1		Intron			XP_016880878.1
XM_017025390.1		Intron			XP_016880879.1
XM_017025391.1		Intron			XP_016880880.1
XM_017025392.1		Intron			XP_016880881.1
XM_017025393.1		Intron			XP_016880882.1
XM_017025394.1		Intron			XP_016880883.1
XM_017025395.1		Intron			XP_016880884.1

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