Product Details

SNP ID

rs587674269

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:112087725 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGAGGCCGGGGTAACTGGCAGGTAA[C/T]TAGGCTTTGGAGTGGTATTTTAAAA

Phenotype

MIM: 607345

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

FAM229B PubMed Links

Gene Details

Gene

FAM229B

Gene Name

family with sequence similarity 229 member B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001033564.2		Intron			NP_001028736.1
XM_017011174.1		Intron			XP_016866663.1
XM_017011175.1		Intron			XP_016866664.1

Gene

TUBE1

Gene Name

tubulin epsilon 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_016262.4		Intron			NP_057346.1
XM_011535875.2		Intron			XP_011534177.1
XM_017010918.1		Intron			XP_016866407.1

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