Product Details

SNP ID

rs772769052

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.12:52691190 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTACTCCAAGATCCGCCTGTGGGAG[G/T]TGTTGGTGGAGGTCTGGATGATCTG

Phenotype

MIM: 611158

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

KRT77 PubMed Links

Additional Information

For this assay, SNP(s) [rs113232993] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene

KRT77

Gene Name

keratin 77

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_175078.2	1503	Missense Mutation	AAC,ACC	N571T	NP_778253.2
XM_011538288.2	1503	Missense Mutation	AAC,ACC	N338T	XP_011536590.1
XM_011538289.2	1503	Intron			XP_011536591.1

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