Product Details

SNP ID

rs201973871

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:77020729 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCTGTGCCACTCGGCAAGCCAGAGC[C/G]TGCCTGCCATGCCGGTGCCCATCAA

Phenotype

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

FOXB2 PubMed Links

Gene Details

Gene

FOXB2

Gene Name

forkhead box B2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001013735.1	1075	Missense Mutation	CTG,GTG	L359V	NP_001013757.1

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