Product Details

SNP ID

rs3809357

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.13:20566642 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

CTTCCAAGGTTCACAAGGCTCGTGC[A/T]GCGGCTCCGGGAGTTATGTCACAGT

Phenotype

MIM: 600595

Polymorphism

A/T, Transversion 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	197	Intron			NP_001305420.1
NM_001318493.1	197	Intron			NP_001305422.1
NM_006531.4	197	Intron			NP_006522.2
NM_175605.4	197	Intron			NP_783195.2
XM_005266553.2	197	UTR 5			XP_005266610.1
XM_006719870.3	197	Intron			XP_006719933.1
XM_011535241.2	197	Intron			XP_011533543.1
XM_011535242.1	197	UTR 5			XP_011533544.1
XM_011535243.1	197	UTR 5			XP_011533545.1
XM_017020757.1	197	UTR 5			XP_016876246.1
XM_017020758.1	197	Intron			XP_016876247.1
XM_017020759.1	197	Intron			XP_016876248.1
XM_017020760.1	197	Intron			XP_016876249.1
XM_017020761.1	197	Intron			XP_016876250.1
XM_017020762.1	197	Intron			XP_016876251.1
XM_017020763.1	197	Intron			XP_016876252.1
XM_017020764.1	197	Intron			XP_016876253.1
XM_017020765.1	197	Intron			XP_016876254.1
XM_017020766.1	197	Intron			XP_016876255.1
XM_017020767.1	197	Intron			XP_016876256.1
XM_017020768.1	197	Intron			XP_016876257.1
XM_017020769.1	197	Intron			XP_016876258.1
XM_017020770.1	197	Intron			XP_016876259.1
XM_017020771.1	197	UTR 5			XP_016876260.1
XM_017020772.1	197	Intron			XP_016876261.1
XM_017020773.1	197	UTR 5			XP_016876262.1
XM_017020774.1	197	Intron			XP_016876263.1
XM_017020775.1	197	Intron			XP_016876264.1
XM_017020776.1	197	Intron			XP_016876265.1

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