Product Details

SNP ID

rs55683527

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:112087265 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACCGCGGCGTGCTCCCTTAGTGCCA[A/G]GTCCCAGAAGCAGCAGCCGATCTGG

Phenotype

MIM: 607345

Polymorphism

A/G, 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	126	Intron			NP_001028736.1
XM_017011174.1	126	Intron			XP_016866663.1
XM_017011175.1	126	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	126	Silent Mutation	CTG,TTG	L23L	NP_057346.1
XM_011535875.2	126	UTR 5			XP_011534177.1
XM_017010918.1	126	UTR 5			XP_016866407.1

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