Product Details

SNP ID
rs138617718
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:94014598 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AAAGATCCCTTAAATCCTTTATTTG[A/G]TTCTCCAAATTAACAAGTTCCTTGT
Phenotype
MIM: 608922
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
ARL13B PubMed Links

Gene Details

Gene
ARL13B
Gene Name
ADP ribosylation factor like GTPase 13B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001174150.1 929 Intron NP_001167621.1
NM_001174151.1 929 Intron NP_001167622.1
NM_001321328.1 929 Intron NP_001308257.1
NM_144996.3 929 Intron NP_659433.2
NM_182896.2 929 Intron NP_878899.1
XM_006713532.3 929 Intron XP_006713595.1
XM_011512532.2 929 Intron XP_011510834.1
XM_011512533.2 929 Intron XP_011510835.1
XM_011512534.2 929 Intron XP_011510836.1
XM_011512535.2 929 Intron XP_011510837.1
XM_017005853.1 929 Intron XP_016861342.1
Gene
STX19
Gene Name
syntaxin 19
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001001850.2 929 Silent Mutation AAC,AAT N224N NP_001001850.1
XM_011512842.2 929 Silent Mutation AAC,AAT N224N XP_011511144.1

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