Product Details

SNP ID

rs1898466

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.8:84185557 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CGAATCTGCTGGAAATTTTTCTGTC[C/T]AAATAAATTTCCTGAAGGCATACAT

Phenotype

MIM: 614648

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

RALYL PubMed Links

Gene Details

Gene

RALYL

Gene Name

RALY RNA binding protein-like

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001100391.1		Intron			NP_001093861.1
NM_001100392.1		Intron			NP_001093862.1
NM_001100393.1		Intron			NP_001093863.1
NM_001287243.1		Intron			NP_001274172.1
NM_001287244.1		Intron			NP_001274173.1
NM_173848.5		Intron			NP_776247.3
XM_011517462.2		Intron			XP_011515764.1
XM_017013058.1		Intron			XP_016868547.1
XM_017013059.1		Intron			XP_016868548.1
XM_017013060.1		Intron			XP_016868549.1
XM_017013061.1		Intron			XP_016868550.1
XM_017013062.1		Intron			XP_016868551.1
XM_017013063.1		Intron			XP_016868552.1
XM_017013064.1		Intron			XP_016868553.1
XM_017013065.1		Intron			XP_016868554.1
XM_017013066.1		Intron			XP_016868555.1
XM_017013067.1		Intron			XP_016868556.1
XM_017013068.1		Intron			XP_016868557.1
XM_017013069.1		Intron			XP_016868558.1
XM_017013070.1		Intron			XP_016868559.1
XM_017013071.1		Intron			XP_016868560.1
XM_017013072.1		Intron			XP_016868561.1
XM_017013073.1		Intron			XP_016868562.1
XM_017013074.1		Intron			XP_016868563.1
XM_017013075.1		Intron			XP_016868564.1
XM_017013076.1		Intron			XP_016868565.1
XM_017013077.1		Intron			XP_016868566.1
XM_017013078.1		Intron			XP_016868567.1
XM_017013079.1		Intron			XP_016868568.1
XM_017013080.1		Intron			XP_016868569.1
XM_017013081.1		Intron			XP_016868570.1
XM_017013082.1		Intron			XP_016868571.1
XM_017013083.1		Intron			XP_016868572.1
XM_017013084.1		Intron			XP_016868573.1
XM_017013085.1		Intron			XP_016868574.1
XM_017013086.1		Intron			XP_016868575.1
XM_017013087.1		Intron			XP_016868576.1

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