Product Details

SNP ID

rs6698208

Assay Type

Functionally tested

NCBI dbSNP Submissions

13

Location

Chr.1:50066153 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TTTTGCAGTTGATCTACCCTACCAC[C/T]CTTACATTCCTTCTAGAAATAAGAG

Phenotype

MIM: 168360

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

ELAVL4 PubMed Links

Gene Details

Gene

ELAVL4

Gene Name

ELAV like neuron-specific RNA binding protein 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001144774.2		Intron			NP_001138246.1
NM_001144775.2		Intron			NP_001138247.2
NM_001144776.2		Intron			NP_001138248.1
NM_001144777.2		Intron			NP_001138249.1
NM_001294348.1		Intron			NP_001281277.1
NM_001324208.1		Intron			NP_001311137.1
NM_001324209.1		Intron			NP_001311138.1
NM_001324212.1		Intron			NP_001311141.1
NM_001324213.1		Intron			NP_001311142.1
NM_001324214.1		Intron			NP_001311143.1
NM_001324215.1		Intron			NP_001311144.1
NM_001324216.1		Intron			NP_001311145.1
NM_001324217.1		Intron			NP_001311146.1
NM_021952.4		Intron			NP_068771.2
XM_006710411.3		Intron			XP_006710474.1
XM_011540889.2		Intron			XP_011539191.1
XM_011540890.2		Intron			XP_011539192.1
XM_011540893.2		Intron			XP_011539195.1
XM_011540894.2		Intron			XP_011539196.1
XM_011540895.2		Intron			XP_011539197.1
XM_017000538.1		Intron			XP_016856027.1
XM_017000539.1		Intron			XP_016856028.1
XM_017000540.1		Intron			XP_016856029.1
XM_017000541.1		Intron			XP_016856030.1
XM_017000542.1		Intron			XP_016856031.1

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