Product Details

SNP ID
rs150138947
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.18:70004977 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTGGCAAAGAAAATTTAGTACAAAA[A/G]TAAGACGAAGATCACAGATGCATTT
Phenotype
MIM: 610436
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
RTTN PubMed Links

Gene Details

Gene
RTTN
Gene Name
rotatin
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001318520.1 Intron NP_001305449.1
NM_173630.3 Intron NP_775901.3
XM_006722434.3 Intron XP_006722497.1
XM_006722435.3 Intron XP_006722498.1
XM_011525902.2 Intron XP_011524204.1
XM_011525903.2 Intron XP_011524205.1
XM_011525904.2 Intron XP_011524206.1
XM_011525905.2 Intron XP_011524207.1
XM_011525906.2 Intron XP_011524208.1
XM_011525907.2 Intron XP_011524209.1
XM_011525908.2 Intron XP_011524210.1
XM_017025693.1 Intron XP_016881182.1
XM_017025694.1 Intron XP_016881183.1
XM_017025695.1 Intron XP_016881184.1
XM_017025696.1 Intron XP_016881185.1

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