Product Details

SNP ID

rs6540120

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.16:87953818 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CTGGATGGGTTAGCTTGCACACGAG[C/T]CAGCCTGATATTTTCCTTTCTTCTG

Phenotype

MIM: 611564

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

BANP PubMed Links

Gene Details

Gene

BANP

Gene Name

BTG3 associated nuclear protein

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001173539.1		Intron			NP_001167010.1
NM_001173540.1		Intron			NP_001167011.1
NM_001173541.1		Intron			NP_001167012.1
NM_001173542.1		Intron			NP_001167013.1
NM_001173543.1		Intron			NP_001167014.1
NM_017869.3		Intron			NP_060339.2
NM_079837.2		Intron			NP_524576.2
XM_005256008.3		Intron			XP_005256065.1
XM_005256009.3		Intron			XP_005256066.1
XM_011523170.2		Intron			XP_011521472.1
XM_011523172.2		Intron			XP_011521474.1
XM_011523174.2		Intron			XP_011521476.1
XM_011523175.2		Intron			XP_011521477.1
XM_011523176.2		Intron			XP_011521478.1
XM_011523177.2		Intron			XP_011521479.1
XM_011523178.2		Intron			XP_011521480.1
XM_011523179.2		Intron			XP_011521481.1
XM_011523180.2		Intron			XP_011521482.1
XM_011523181.2		Intron			XP_011521483.1
XM_011523182.1		Intron			XP_011521484.1
XM_011523183.2		Intron			XP_011521485.1
XM_011523184.2		Intron			XP_011521486.1
XM_011523186.2		Intron			XP_011521488.1
XM_017023378.1		Intron			XP_016878867.1
XM_017023379.1		Intron			XP_016878868.1
XM_017023380.1		Intron			XP_016878869.1
XM_017023381.1		Intron			XP_016878870.1
XM_017023382.1		Intron			XP_016878871.1
XM_017023383.1		Intron			XP_016878872.1

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