Product Details

SNP ID

rs190229494

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:35619255 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCGCCTGCTGGGCCTCCAGCGCCAC[A/G]TGCCGCCGCTGGCACTGGCTCGGGT

Phenotype

MIM: 612206

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

FJX1 PubMed Links

Gene Details

Gene

FJX1

Gene Name

four jointed box 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_014344.3	1069	Missense Mutation	ATG,GTG	M207V	NP_055159.2

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