Product Details

SNP ID

rs144586198

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.12:52692487 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTCCACATCCAGGGACAGCTTGACC[C/G]CCAGCATGGCCTGGTAGTCACGCAG

Phenotype

MIM: 611158

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

KRT77 PubMed Links

Gene Details

Gene

KRT77

Gene Name

keratin 77

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_175078.2	1152	Missense Mutation	GCG,GGG	A454G	NP_778253.2
XM_011538288.2	1152	Missense Mutation	GCG,GGG	A221G	XP_011536590.1
XM_011538289.2	1152	Intron			XP_011536591.1

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