Product Details

SNP ID

rs16944564

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:60684370 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TGCCAGAAGGGAGAAAAGCAATATA[C/G]ACTCTGCACTCCTTAACTAGATATT

Phenotype

MIM: 607470

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

BCAS3 PubMed Links

Gene Details

Gene

BCAS3

Gene Name

BCAS3, microtubule associated cell migration factor

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001099432.1		Intron			NP_001092902.1
NM_001320470.1		Intron			NP_001307399.1
NM_017679.3		Intron			NP_060149.3
XM_005257472.1		Intron			XP_005257529.1
XM_011524939.1		Intron			XP_011523241.1
XM_011524940.1		Intron			XP_011523242.1
XM_011524941.1		Intron			XP_011523243.1
XM_011524942.2		Intron			XP_011523244.1
XM_011524943.2		Intron			XP_011523245.1
XM_011524944.1		Intron			XP_011523246.1
XM_011524945.2		Intron			XP_011523247.1
XM_011524946.2		Intron			XP_011523248.1
XM_011524947.1		Intron			XP_011523249.1
XM_011524948.2		Intron			XP_011523250.1
XM_011524949.2		Intron			XP_011523251.1
XM_011524950.1		Intron			XP_011523252.1
XM_011524951.2		Intron			XP_011523253.1
XM_017024783.1		Intron			XP_016880272.1
XM_017024784.1		Intron			XP_016880273.1
XM_017024785.1		Intron			XP_016880274.1
XM_017024786.1		Intron			XP_016880275.1
XM_017024787.1		Intron			XP_016880276.1
XM_017024788.1		Intron			XP_016880277.1
XM_017024789.1		Intron			XP_016880278.1
XM_017024790.1		Intron			XP_016880279.1
XM_017024791.1		Intron			XP_016880280.1
XM_017024792.1		Intron			XP_016880281.1
XM_017024793.1		Intron			XP_016880282.1
XM_017024794.1		Intron			XP_016880283.1
XM_017024795.1		Intron			XP_016880284.1
XM_017024796.1		Intron			XP_016880285.1

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