Product Details

SNP ID

rs138215044

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.15:89472828 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTCCTGAGGGCTTGAAGGTGGGGTC[A/C]TCAGGGATGTAGACAGTGCTGTTCC

Phenotype

MIM: 605381

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

LOC105371031 PubMed Links

Gene Details

Gene

LOC105371031

Gene Name

translation initiation factor IF-2-like

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
XM_017022800.1	1416	Intron			XP_016878289.1

Gene

RHCG

Gene Name

Rh family C glycoprotein

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001321041.1	1416	Missense Mutation	GAG,GAT	E449D	NP_001307970.1
NM_016321.2	1416	Missense Mutation	GAG,GAT	E449D	NP_057405.1

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