Product Details

SNP ID

rs1190637

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:104954404 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GGGGAAGGCACAGAAAAAACAGTGC[C/T]ATATTCTTAAATTGGTGAGTGATTA

Phenotype

MIM: 611044

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

LIN28B PubMed Links

Gene Details

Gene

LIN28B

Gene Name

lin-28 homolog B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001004317.3		Intron			NP_001004317.1
XM_006715477.2		Intron			XP_006715540.2
XM_011535818.2		Intron			XP_011534120.1

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