Product Details

SNP ID

rs114064150

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:85433130 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTGCATCGTCCAGAGTGGTGAGCAG[C/T]CCCTCCATTTCCACCTCAGTTTCCA

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

SH2D6 PubMed Links

Gene Details

Gene

SH2D6

Gene Name

SH2 domain containing 6

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_201594.2		Intron			NP_963888.2
XM_011532783.1		Intron			XP_011531085.1
XM_011532796.2		Intron			XP_011531098.1
XM_017003834.1		Intron			XP_016859323.1
XM_017003835.1		Intron			XP_016859324.1
XM_017003836.1		Intron			XP_016859325.1
XM_017003837.1		Intron			XP_016859326.1
XM_017003838.1		Intron			XP_016859327.1
XM_017003839.1		Intron			XP_016859328.1
XM_017003840.1		Intron			XP_016859329.1
XM_017003841.1		Intron			XP_016859330.1
XM_017003842.1		Intron			XP_016859331.1
XM_017003843.1		Intron			XP_016859332.1
XM_017003844.1		Intron			XP_016859333.1
XM_017003845.1		Intron			XP_016859334.1
XM_017003846.1		Intron			XP_016859335.1
XM_017003847.1		Intron			XP_016859336.1
XM_017003848.1		Intron			XP_016859337.1
XM_017003849.1		Intron			XP_016859338.1
XM_017003850.1		Intron			XP_016859339.1
XM_017003851.1		Intron			XP_016859340.1
XM_017003852.1		Intron			XP_016859341.1
XM_017003853.1		Intron			XP_016859342.1
XM_017003854.1		Intron			XP_016859343.1
XM_017003855.1		Intron			XP_016859344.1
XM_017003856.1		Intron			XP_016859345.1
XM_017003857.1		Intron			XP_016859346.1
XM_017003858.1		Intron			XP_016859347.1
XM_017003859.1		Intron			XP_016859348.1
XM_017003860.1		Intron			XP_016859349.1

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