Product Details

SNP ID

rs4843748

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.16:87959323 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TTTTAAAATGTAAAACCCATTCCTG[A/G]CTCACAGGCTGCATAGAAGCAGGTG

Phenotype

MIM: 611564

Polymorphism

A/G, 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	636	Intron			NP_001167010.1
NM_001173540.1	636	Intron			NP_001167011.1
NM_001173541.1	636	Intron			NP_001167012.1
NM_001173542.1	636	Intron			NP_001167013.1
NM_001173543.1	636	Intron			NP_001167014.1
NM_017869.3	636	Intron			NP_060339.2
NM_079837.2	636	Intron			NP_524576.2
XM_005256008.3	636	Intron			XP_005256065.1
XM_005256009.3	636	Intron			XP_005256066.1
XM_011523170.2	636	Intron			XP_011521472.1
XM_011523172.2	636	Intron			XP_011521474.1
XM_011523174.2	636	Intron			XP_011521476.1
XM_011523175.2	636	Intron			XP_011521477.1
XM_011523176.2	636	Intron			XP_011521478.1
XM_011523177.2	636	UTR 5			XP_011521479.1
XM_011523178.2	636	Intron			XP_011521480.1
XM_011523179.2	636	Intron			XP_011521481.1
XM_011523180.2	636	Intron			XP_011521482.1
XM_011523181.2	636	Intron			XP_011521483.1
XM_011523182.1	636	Intron			XP_011521484.1
XM_011523183.2	636	Intron			XP_011521485.1
XM_011523184.2	636	Intron			XP_011521486.1
XM_011523186.2	636	Intron			XP_011521488.1
XM_017023378.1	636	Intron			XP_016878867.1
XM_017023379.1	636	Intron			XP_016878868.1
XM_017023380.1	636	Intron			XP_016878869.1
XM_017023381.1	636	Intron			XP_016878870.1
XM_017023382.1	636	Intron			XP_016878871.1
XM_017023383.1	636	Intron			XP_016878872.1

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