Product Details

SNP ID

rs7980833

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.12:80796647 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TTATCTGAGAGTGCCAAAAATATCT[C/G]GTTTATATTTGGGGAAATTGACCTA

Phenotype

MIM: 603380

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

LIN7A PubMed Links

Gene Details

Gene

LIN7A

Gene Name

lin-7 homolog A, crumbs cell polarity complex component

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001324423.1	1750	UTR 3			NP_001311352.1
NM_004664.3	1750	UTR 3			NP_004655.1
XM_011538928.2	1750	UTR 3			XP_011537230.1

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