Product Details

SNP ID

rs1804788

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.13:106491261 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGTCACATCGGCTTCCTGCTCTGTG[C/G]GGCTCGTACTTCCTAGTCTACGGTT

Phenotype

MIM: 600527

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

EFNB2 PubMed Links

Gene Details

Gene

EFNB2

Gene Name

ephrin B2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_004093.3	2857	UTR 3			NP_004084.1
XM_017020406.1	2857	UTR 3			XP_016875895.1

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