Product Details

SNP ID
rs139670254
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.19:14151199 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGGGGCCGGCTGGTGGCGCCGTCCT[C/G]GGCCGTGCAGCTCTCCGACTCGTCC
Phenotype
MIM: 616416
Polymorphism
C/G, Transversion Substitution
Allele Nomenclature
Literature Links
ADGRL1 PubMed Links

Gene Details

Gene
ADGRL1
Gene Name
adhesion G protein-coupled receptor L1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001008701.2 4508 Missense Mutation CAG,GAG Q1367E NP_001008701.1
NM_014921.4 4508 Missense Mutation CAG,GAG Q1362E NP_055736.2
XM_005259818.3 4508 Missense Mutation CAG,GAG Q1386E XP_005259875.1
XM_011527796.2 4508 Missense Mutation CAG,GAG Q1398E XP_011526098.1
XM_011527798.2 4508 Missense Mutation CAG,GAG Q1393E XP_011526100.1
XM_011527801.2 4508 Missense Mutation CAG,GAG Q1318E XP_011526103.1
XM_017026475.1 4508 Missense Mutation CAG,GAG Q1399E XP_016881964.1
XM_017026476.1 4508 Missense Mutation CAG,GAG Q1399E XP_016881965.1
XM_017026477.1 4508 Missense Mutation CAG,GAG Q1392E XP_016881966.1
XM_017026478.1 4508 Missense Mutation CAG,GAG Q1375E XP_016881967.1
XM_017026479.1 4508 Missense Mutation CAG,GAG Q1369E XP_016881968.1
XM_017026480.1 4508 Missense Mutation CAG,GAG Q1313E XP_016881969.1
XM_017026481.1 4508 Intron XP_016881970.1
Gene
LOC100507373
Gene Name
uncharacterized LOC100507373
There are no transcripts associated with this gene.

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