Product Details

SNP ID
rs149433236
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:94014949 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTTCTTTAACTAAATCATTCAAACT[G/T]CTGTTGATGTATTCTGCCTGAATTT
Phenotype
MIM: 608922
Polymorphism
G/T, Transversion 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_001174150.1 578 Intron NP_001167621.1
NM_001174151.1 578 Intron NP_001167622.1
NM_001321328.1 578 Intron NP_001308257.1
NM_144996.3 578 Intron NP_659433.2
NM_182896.2 578 Intron NP_878899.1
XM_006713532.3 578 Intron XP_006713595.1
XM_011512532.2 578 Intron XP_011510834.1
XM_011512533.2 578 Intron XP_011510835.1
XM_011512534.2 578 Intron XP_011510836.1
XM_011512535.2 578 Intron XP_011510837.1
XM_017005853.1 578 Intron XP_016861342.1
Gene
STX19
Gene Name
syntaxin 19
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001001850.2 578 Missense Mutation AGA,AGC R107S NP_001001850.1
XM_011512842.2 578 Missense Mutation AGA,AGC R107S XP_011511144.1

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