Product Details

SNP ID

rs7993213

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.13:95436598 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GAAAATCTCACCCACTGACAATGCT[C/T]CCCTAAGAACAAGTACAATTAAATT

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

CLDN10 PubMed Links

Gene Details

Gene

CLDN10

Gene Name

claudin 10

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001160100.1		Intron			NP_001153572.1
NM_006984.4		Intron			NP_008915.1
NM_182848.3		Intron			NP_878268.1
XM_011521134.2		Intron			XP_011519436.1
XM_017020843.1		Intron			XP_016876332.1
XM_017020844.1		Intron			XP_016876333.1

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