Product Details

SNP ID

rs7200729

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.16:87949449 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CCACTGCCGGAGGGAATATTCTGTG[G/T]CAGCTATCGCACGCACCCTTTCCCT

Phenotype

MIM: 611564

Polymorphism

G/T, Transversion 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	234	Intron			NP_001167010.1
NM_001173540.1	234	Intron			NP_001167011.1
NM_001173541.1	234	Intron			NP_001167012.1
NM_001173542.1	234	Intron			NP_001167013.1
NM_001173543.1	234	Intron			NP_001167014.1
NM_017869.3	234	Intron			NP_060339.2
NM_079837.2	234	Intron			NP_524576.2
XM_005256008.3	234	Intron			XP_005256065.1
XM_005256009.3	234	Intron			XP_005256066.1
XM_011523170.2	234	Intron			XP_011521472.1
XM_011523172.2	234	Intron			XP_011521474.1
XM_011523174.2	234	Intron			XP_011521476.1
XM_011523175.2	234	Intron			XP_011521477.1
XM_011523176.2	234	UTR 5			XP_011521478.1
XM_011523177.2	234	Intron			XP_011521479.1
XM_011523178.2	234	Intron			XP_011521480.1
XM_011523179.2	234	Intron			XP_011521481.1
XM_011523180.2	234	Intron			XP_011521482.1
XM_011523181.2	234	Intron			XP_011521483.1
XM_011523182.1	234	Intron			XP_011521484.1
XM_011523183.2	234	Intron			XP_011521485.1
XM_011523184.2	234	Intron			XP_011521486.1
XM_011523186.2	234	Intron			XP_011521488.1
XM_017023378.1	234	Intron			XP_016878867.1
XM_017023379.1	234	Intron			XP_016878868.1
XM_017023380.1	234	Intron			XP_016878869.1
XM_017023381.1	234	Intron			XP_016878870.1
XM_017023382.1	234	Intron			XP_016878871.1
XM_017023383.1	234	Intron			XP_016878872.1

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