Product Details

SNP ID
rs2667688
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.16:1511445 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGAAAGTCCCTCAGCAGCTGTGCAC[A/G]GGCCTGCTCACCGTGCGTGTGCGGG
Phenotype
MIM: 614620 MIM: 611140
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
IFT140 PubMed Links

Gene Details

Gene
IFT140
Gene Name
intraflagellar transport 140
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_014714.3 Intron NP_055529.2
XM_005255725.4 Intron XP_005255782.1
XM_005255726.3 Intron XP_005255783.1
XM_006720990.3 Intron XP_006721053.1
XM_006720991.3 Intron XP_006721054.1
XM_006720992.3 Intron XP_006721055.1
XM_011522766.2 Intron XP_011521068.1
XM_011522767.2 Intron XP_011521069.1
XM_011522769.2 Intron XP_011521071.1
XM_011522771.2 Intron XP_011521073.1
XM_011522772.2 Intron XP_011521074.1
XM_017023910.1 Intron XP_016879399.1
XM_017023911.1 Intron XP_016879400.1
Gene
TELO2
Gene Name
telomere maintenance 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_016111.3 Intron NP_057195.2
XM_011522773.2 Intron XP_011521075.1
XM_011522774.2 Intron XP_011521076.1
XM_011522775.2 Intron XP_011521077.1
XM_011522776.2 Intron XP_011521078.1
XM_011522777.2 Intron XP_011521079.1
XM_011522778.2 Intron XP_011521080.1
XM_017023914.1 Intron XP_016879403.1

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