Product Details

SNP ID

rs199900544

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:47744303 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CAACGCTTCCAACACGCATATCTTT[A/G]CTTTCCAAGAAACCCAGTTCATTGC

Phenotype

MIM: 604895

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

TBX21 PubMed Links

Gene Details

Gene

TBX21

Gene Name

T-box 21

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_013351.1	1155	Missense Mutation	ACT,GCT	T293A	NP_037483.1
XM_011524698.2	1155	Missense Mutation	ACT,GCT	T314A	XP_011523000.1

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