Product Details

SNP ID

rs9322975

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.14:37210069 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TTTAATTTAATAATATCTTGTATGT[A/G]TGTGTTTTTGAAAAACGCTCAAACT

Phenotype

MIM: 606850

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

MIPOL1 PubMed Links

Gene Details

Gene

MIPOL1

Gene Name

mirror-image polydactyly 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001195296.1		Intron			NP_001182225.1
NM_001195297.1		Intron			NP_001182226.1
NM_138731.6		Intron			NP_620059.1
XM_011536463.2		Intron			XP_011534765.1
XM_011536467.2		Intron			XP_011534769.1
XM_017020991.1		Intron			XP_016876480.1
XM_017020992.1		Intron			XP_016876481.1
XM_017020993.1		Intron			XP_016876482.1
XM_017020994.1		Intron			XP_016876483.1
XM_017020995.1		Intron			XP_016876484.1
XM_017020996.1		Intron			XP_016876485.1
XM_017020997.1		Intron			XP_016876486.1
XM_017020998.1		Intron			XP_016876487.1
XM_017020999.1		Intron			XP_016876488.1
XM_017021000.1		Intron			XP_016876489.1
XM_017021001.1		Intron			XP_016876490.1
XM_017021002.1		Intron			XP_016876491.1
XM_017021003.1		Intron			XP_016876492.1
XM_017021004.1		Intron			XP_016876493.1
XM_017021005.1		Intron			XP_016876494.1
XM_017021006.1		Intron			XP_016876495.1
XM_017021007.1		Intron			XP_016876496.1
XM_017021008.1		Intron			XP_016876497.1
XM_017021009.1		Intron			XP_016876498.1
XM_017021010.1		Intron			XP_016876499.1
XM_017021011.1		Intron			XP_016876500.1
XM_017021012.1		Intron			XP_016876501.1
XM_017021013.1		Intron			XP_016876502.1
XM_017021014.1		Intron			XP_016876503.1
XM_017021015.1		Intron			XP_016876504.1
XM_017021016.1		Intron			XP_016876505.1
XM_017021017.1		Intron			XP_016876506.1
XM_017021018.1		Intron			XP_016876507.1
XM_017021019.1		Intron			XP_016876508.1

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