Product Details

SNP ID
rs144715706
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:94015119 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCCTGTAGTTTTTGGATTTCATGTA[A/G]GTGTCTCTCAGCTACAGGCTCTCTT
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_001174150.1 408 Intron NP_001167621.1
NM_001174151.1 408 Intron NP_001167622.1
NM_001321328.1 408 Intron NP_001308257.1
NM_144996.3 408 Intron NP_659433.2
NM_182896.2 408 Intron NP_878899.1
XM_006713532.3 408 Intron XP_006713595.1
XM_011512532.2 408 Intron XP_011510834.1
XM_011512533.2 408 Intron XP_011510835.1
XM_011512534.2 408 Intron XP_011510836.1
XM_011512535.2 408 Intron XP_011510837.1
XM_017005853.1 408 Intron XP_016861342.1
Gene
STX19
Gene Name
syntaxin 19
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001001850.2 408 Silent Mutation CTA,TTA L51L NP_001001850.1
XM_011512842.2 408 Silent Mutation CTA,TTA L51L XP_011511144.1

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