Product Details
- SNP ID
-
rs201672648
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.3:18349215 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TAATGTCTGTGTTTCCTTCCACTGA[C/T]AGCTCTTCTTCTAGTTTCACTGAAA
- Phenotype
-
MIM: 602075
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
SATB1
PubMed Links
Gene Details
- Gene
- SATB1
- Gene Name
- SATB homeobox 1
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_001131010.3 |
2528 |
Silent Mutation |
CTA,CTG |
L749L |
NP_001124482.1 |
| NM_001195470.2 |
2528 |
Silent Mutation |
CTA,CTG |
L781L |
NP_001182399.1 |
| NM_001322871.1 |
2528 |
Silent Mutation |
CTA,CTG |
L781L |
NP_001309800.1 |
| NM_001322872.1 |
2528 |
Silent Mutation |
CTA,CTG |
L749L |
NP_001309801.1 |
| NM_001322873.1 |
2528 |
Silent Mutation |
CTA,CTG |
L749L |
NP_001309802.1 |
| NM_001322874.1 |
2528 |
Silent Mutation |
CTA,CTG |
L749L |
NP_001309803.1 |
| NM_001322875.1 |
2528 |
Silent Mutation |
CTA,CTG |
L749L |
NP_001309804.1 |
| NM_001322876.1 |
2528 |
Silent Mutation |
CTA,CTG |
L677L |
NP_001309805.1 |
| NM_002971.5 |
2528 |
Silent Mutation |
CTA,CTG |
L749L |
NP_002962.1 |
| XM_011533988.2 |
2528 |
Silent Mutation |
CTA,CTG |
L781L |
XP_011532290.1 |
| XM_011533989.2 |
2528 |
Silent Mutation |
CTA,CTG |
L781L |
XP_011532291.1 |
| XM_011533990.2 |
2528 |
Intron |
|
|
XP_011532292.1 |
View Full Product Details