Product Details
- SNP ID
-
rs141410755
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
6
- Location
-
Chr.1:31728035 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CCCGGGGGGACTCACGGTGCACACG[C/G]TCCGCTCGGCTGCCCCACCCGAGGA
- Phenotype
-
MIM: 602683
- Polymorphism
- C/G, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
ADGRB2
PubMed Links
Gene Details
- Gene
- ADGRB2
- Gene Name
- adhesion G protein-coupled receptor B2
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001294335.1 |
4985 |
Missense Mutation |
ACC,AGC |
T1520S |
NP_001281264.1 |
NM_001294336.1 |
4985 |
Missense Mutation |
ACC,AGC |
T1487S |
NP_001281265.1 |
XM_011541848.2 |
4985 |
Missense Mutation |
ACC,AGC |
T1521S |
XP_011540150.1 |
XM_011541849.2 |
4985 |
Missense Mutation |
ACC,AGC |
T1509S |
XP_011540151.1 |
XM_011541858.2 |
4985 |
Missense Mutation |
ACC,AGC |
T1218S |
XP_011540160.1 |
XM_017001899.1 |
4985 |
Missense Mutation |
ACC,AGC |
T1521S |
XP_016857388.1 |
XM_017001900.1 |
4985 |
Missense Mutation |
ACC,AGC |
T1520S |
XP_016857389.1 |
XM_017001901.1 |
4985 |
Intron |
|
|
XP_016857390.1 |
XM_017001902.1 |
4985 |
Intron |
|
|
XP_016857391.1 |
XM_017001903.1 |
4985 |
Missense Mutation |
ACC,AGC |
T1498S |
XP_016857392.1 |
XM_017001904.1 |
4985 |
Missense Mutation |
ACC,AGC |
T1488S |
XP_016857393.1 |
XM_017001905.1 |
4985 |
Missense Mutation |
ACC,AGC |
T1487S |
XP_016857394.1 |
XM_017001906.1 |
4985 |
Intron |
|
|
XP_016857395.1 |
XM_017001907.1 |
4985 |
Missense Mutation |
ACC,AGC |
T1466S |
XP_016857396.1 |
XM_017001908.1 |
4985 |
Missense Mutation |
ACC,AGC |
T1466S |
XP_016857397.1 |
XM_017001909.1 |
4985 |
Intron |
|
|
XP_016857398.1 |
XM_017001910.1 |
4985 |
Missense Mutation |
ACC,AGC |
T1433S |
XP_016857399.1 |
XM_017001911.1 |
4985 |
Intron |
|
|
XP_016857400.1 |
XM_017001912.1 |
4985 |
Missense Mutation |
ACC,AGC |
T1411S |
XP_016857401.1 |
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