Product Details

SNP ID

rs7998003

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.13:20584971 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ATTCTACAATGCATAGGGCAGCCCC[C/T]GGTAATAAAGAGCTATCCAGCCGAA

Phenotype

MIM: 600595

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

IFT88 PubMed Links

Gene Details

Gene

IFT88

Gene Name

intraflagellar transport 88

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001318491.1		Intron			NP_001305420.1
NM_001318493.1		Intron			NP_001305422.1
NM_006531.4		Intron			NP_006522.2
NM_175605.4		Intron			NP_783195.2
XM_005266553.2		Intron			XP_005266610.1
XM_006719870.3		Intron			XP_006719933.1
XM_011535241.2		Intron			XP_011533543.1
XM_011535242.1		Intron			XP_011533544.1
XM_011535243.1		Intron			XP_011533545.1
XM_017020757.1		Intron			XP_016876246.1
XM_017020758.1		Intron			XP_016876247.1
XM_017020759.1		Intron			XP_016876248.1
XM_017020760.1		Intron			XP_016876249.1
XM_017020761.1		Intron			XP_016876250.1
XM_017020762.1		Intron			XP_016876251.1
XM_017020763.1		Intron			XP_016876252.1
XM_017020764.1		Intron			XP_016876253.1
XM_017020765.1		Intron			XP_016876254.1
XM_017020766.1		Intron			XP_016876255.1
XM_017020767.1		Intron			XP_016876256.1
XM_017020768.1		Intron			XP_016876257.1
XM_017020769.1		Intron			XP_016876258.1
XM_017020770.1		Intron			XP_016876259.1
XM_017020771.1		Intron			XP_016876260.1
XM_017020772.1		Intron			XP_016876261.1
XM_017020773.1		Intron			XP_016876262.1
XM_017020774.1		Intron			XP_016876263.1
XM_017020775.1		Intron			XP_016876264.1
XM_017020776.1		Intron			XP_016876265.1

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