Product Details

SNP ID

rs10146011

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.14:88616518 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TAGGTTTGGTGAAAAGCTAATTACA[A/G]CTTTTGTAGGATGGTTCCAAAGATG

Phenotype

MIM: 613279

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

EML5 PubMed Links

Gene Details

Gene

EML5

Gene Name

echinoderm microtubule associated protein like 5

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_183387.2	5939	Intron			NP_899243.1
XM_006720070.3	5939	Intron			XP_006720133.1
XM_011536528.2	5939	Silent Mutation	CTG,TTG	L2002L	XP_011534830.1
XM_011536530.2	5939	Silent Mutation	CTG,TTG	L1999L	XP_011534832.1
XM_011536531.2	5939	Silent Mutation	CTG,TTG	L1994L	XP_011534833.1
XM_011536532.2	5939	Silent Mutation	CTG,TTG	L1994L	XP_011534834.1
XM_011536533.2	5939	Silent Mutation	CTG,TTG	L1956L	XP_011534835.1
XM_011536534.2	5939	Silent Mutation	CTG,TTG	L1943L	XP_011534836.1
XM_011536536.2	5939	Intron			XP_011534838.1
XM_011536538.2	5939	Intron			XP_011534840.1
XM_017021062.1	5939	Intron			XP_016876551.1
XM_017021063.1	5939	Silent Mutation	CTG,TTG	L1995L	XP_016876552.1
XM_017021064.1	5939	Silent Mutation	CTG,TTG	L1964L	XP_016876553.1
XM_017021065.1	5939	Intron			XP_016876554.1
XM_017021066.1	5939	Silent Mutation	CTG,TTG	L1946L	XP_016876555.1
XM_017021067.1	5939	Silent Mutation	CTG,TTG	L1945L	XP_016876556.1
XM_017021068.1	5939	Silent Mutation	CTG,TTG	L1944L	XP_016876557.1
XM_017021069.1	5939	Silent Mutation	CTG,TTG	L1943L	XP_016876558.1
XM_017021070.1	5939	Intron			XP_016876559.1

Gene

ZC3H14

Gene Name

zinc finger CCCH-type containing 14

There are no transcripts associated with this gene.

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