Product Details
- SNP ID
-
rs200166375
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.7:93131481 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GGGAATTTGTATTTTGTGCTTTATC[A/G]AAGTACTGCTCTATTTTGGCCTTGT
- Phenotype
-
MIM: 611170
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
SAMD9L
PubMed Links
Gene Details
- Gene
- SAMD9L
- Gene Name
- sterile alpha motif domain containing 9 like
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_001303496.1 |
4529 |
Silent Mutation |
TTC,TTT |
F1497F |
NP_001290425.1 |
| NM_001303497.1 |
4529 |
Silent Mutation |
TTC,TTT |
F1497F |
NP_001290426.1 |
| NM_001303498.1 |
4529 |
Silent Mutation |
TTC,TTT |
F1497F |
NP_001290427.1 |
| NM_001303500.1 |
4529 |
Silent Mutation |
TTC,TTT |
F1497F |
NP_001290429.1 |
| NM_152703.3 |
4529 |
Silent Mutation |
TTC,TTT |
F1497F |
NP_689916.2 |
| XM_005250193.3 |
4529 |
Silent Mutation |
TTC,TTT |
F1497F |
XP_005250250.1 |
| XM_006715890.1 |
4529 |
Silent Mutation |
TTC,TTT |
F1497F |
XP_006715953.1 |
| XM_011515903.2 |
4529 |
Silent Mutation |
TTC,TTT |
F1497F |
XP_011514205.1 |
| XM_017011822.1 |
4529 |
Silent Mutation |
TTC,TTT |
F1497F |
XP_016867311.1 |
| XM_017011823.1 |
4529 |
Silent Mutation |
TTC,TTT |
F1497F |
XP_016867312.1 |
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