Product Details

SNP ID
rs202036799
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:94015209 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCTGTTTCTGTAGTTGATACATGAC[C/T]GTCTCTAGAGAGTTCAATTTCCTTT
Phenotype
MIM: 608922
Polymorphism
C/T, 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_001174150.1 318 Intron NP_001167621.1
NM_001174151.1 318 Intron NP_001167622.1
NM_001321328.1 318 Intron NP_001308257.1
NM_144996.3 318 Intron NP_659433.2
NM_182896.2 318 Intron NP_878899.1
XM_006713532.3 318 Intron XP_006713595.1
XM_011512532.2 318 Intron XP_011510834.1
XM_011512533.2 318 Intron XP_011510835.1
XM_011512534.2 318 Intron XP_011510836.1
XM_011512535.2 318 Intron XP_011510837.1
XM_017005853.1 318 Intron XP_016861342.1
Gene
STX19
Gene Name
syntaxin 19
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001001850.2 318 Missense Mutation AGT,GGT S21G NP_001001850.1
XM_011512842.2 318 Missense Mutation AGT,GGT S21G XP_011511144.1

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