Product Details
- SNP ID
-
rs148170808
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.19:49343356 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- AAGCCACCACTGCTGATGCTGCCAC[C/T]GGCCCCTGCCTCCTCACCACTTGGG
- Phenotype
-
MIM: 151523
MIM: 601729
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
CD37
PubMed Links
Gene Details
- Gene
- CD37
- Gene Name
- CD37 molecule
There are no transcripts associated with this gene.
- Gene
- TEAD2
- Gene Name
- TEA domain transcription factor 2
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001256658.1 |
1327 |
Missense Mutation |
AGT,GGT |
S321G |
NP_001243587.1 |
NM_001256659.1 |
1327 |
Missense Mutation |
AGT,GGT |
S321G |
NP_001243588.1 |
NM_001256660.1 |
1327 |
Missense Mutation |
AGT,GGT |
S322G |
NP_001243589.1 |
NM_001256661.1 |
1327 |
Missense Mutation |
AGT,GGT |
S322G |
NP_001243590.1 |
NM_001256662.1 |
1327 |
Missense Mutation |
AGT,GGT |
S190G |
NP_001243591.1 |
NM_003598.1 |
1327 |
Missense Mutation |
AGT,GGT |
S318G |
NP_003589.1 |
XM_005259334.3 |
1327 |
Missense Mutation |
AGT,GGT |
S282G |
XP_005259391.1 |
XM_006723424.1 |
1327 |
Missense Mutation |
AGT,GGT |
S322G |
XP_006723487.1 |
XM_006723428.2 |
1327 |
Missense Mutation |
AGT,GGT |
S318G |
XP_006723491.1 |
XM_006723429.2 |
1327 |
Missense Mutation |
AGT,GGT |
S132G |
XP_006723492.1 |
XM_011527398.1 |
1327 |
Missense Mutation |
AGT,GGT |
S325G |
XP_011525700.1 |
XM_011527399.2 |
1327 |
Missense Mutation |
AGT,GGT |
S325G |
XP_011525701.1 |
XM_011527400.2 |
1327 |
Missense Mutation |
AGT,GGT |
S325G |
XP_011525702.1 |
XM_011527401.1 |
1327 |
Missense Mutation |
AGT,GGT |
S325G |
XP_011525703.1 |
XM_011527402.2 |
1327 |
Missense Mutation |
AGT,GGT |
S325G |
XP_011525704.1 |
XM_011527403.1 |
1327 |
Missense Mutation |
AGT,GGT |
S321G |
XP_011525705.1 |
XM_011527404.1 |
1327 |
Missense Mutation |
AGT,GGT |
S325G |
XP_011525706.1 |
XM_011527405.2 |
1327 |
Intron |
|
|
XP_011525707.1 |
XM_011527406.2 |
1327 |
Intron |
|
|
XP_011525708.1 |
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