Product Details
- SNP ID
-
rs202095799
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.19:14151384 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CACAGGTGGCACAGGGGGCTCAGGC[A/G]GTGGAGGGCCCTTGGCCGCGCTGCT
- Phenotype
-
MIM: 616416
- Polymorphism
- A/G, Transition 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 |
4323 |
Missense Mutation |
CCG,CTG |
P1305L |
NP_001008701.1 |
NM_014921.4 |
4323 |
Missense Mutation |
CCG,CTG |
P1300L |
NP_055736.2 |
XM_005259818.3 |
4323 |
Missense Mutation |
CCG,CTG |
P1324L |
XP_005259875.1 |
XM_011527796.2 |
4323 |
Missense Mutation |
CCG,CTG |
P1336L |
XP_011526098.1 |
XM_011527798.2 |
4323 |
Missense Mutation |
CCG,CTG |
P1331L |
XP_011526100.1 |
XM_011527801.2 |
4323 |
Missense Mutation |
CCG,CTG |
P1256L |
XP_011526103.1 |
XM_017026475.1 |
4323 |
Missense Mutation |
CCG,CTG |
P1337L |
XP_016881964.1 |
XM_017026476.1 |
4323 |
Missense Mutation |
CCG,CTG |
P1337L |
XP_016881965.1 |
XM_017026477.1 |
4323 |
Missense Mutation |
CCG,CTG |
P1330L |
XP_016881966.1 |
XM_017026478.1 |
4323 |
Missense Mutation |
CCG,CTG |
P1313L |
XP_016881967.1 |
XM_017026479.1 |
4323 |
Missense Mutation |
CCG,CTG |
P1307L |
XP_016881968.1 |
XM_017026480.1 |
4323 |
Missense Mutation |
CCG,CTG |
P1251L |
XP_016881969.1 |
XM_017026481.1 |
4323 |
Intron |
|
|
XP_016881970.1 |
- Gene
- LOC100507373
- Gene Name
- uncharacterized LOC100507373
There are no transcripts associated with this gene.
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