Product Details

SNP ID

rs17434501

Assay Type

Functionally tested

NCBI dbSNP Submissions

14

Location

Chr.1:206578794 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CACCTGGGAATACCAGAAGCCACGT[A/G]ACTCACTCAGAGCCTCTCCTTAGGG

Phenotype

MIM: 613709 MIM: 607020

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

EIF2D PubMed Links

Gene Details

Gene

EIF2D

Gene Name

eukaryotic translation initiation factor 2D

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001201478.1	4177	Intron			NP_001188407.1
NM_006893.2	4177	Intron			NP_008824.2
XM_005277509.3	4177	Intron			XP_005277566.1
XM_006711196.3	4177	Intron			XP_006711259.1
XM_011509257.2	4177	UTR 3			XP_011507559.1
XM_011509258.2	4177	Intron			XP_011507560.1
XM_017000530.1	4177	Intron			XP_016856019.1
XM_017000531.1	4177	Intron			XP_016856020.1
XM_017000532.1	4177	Intron			XP_016856021.1

Gene

RASSF5

Gene Name

Ras association domain family member 5

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_182663.3	4177	Intron			NP_872604.1
NM_182664.3	4177	Intron			NP_872605.1
NM_182665.3	4177	Intron			NP_872606.1

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