Product Details
- SNP ID
-
rs199540313
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.17:72648817 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GGTTCTCCAACCTGATCTGGGCTTC[A/G]GGGATGATGTCGTCCATGACCACGT
- Phenotype
-
MIM: 616508
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
LINC00511
PubMed Links
Gene Details
- Gene
- LINC00511
- Gene Name
- long intergenic non-protein coding RNA 511
There are no transcripts associated with this gene.
- Gene
- SLC39A11
- Gene Name
- solute carrier family 39 member 11
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_001159770.1 |
1027 |
Silent Mutation |
CCC,CCT |
P312P |
NP_001153242.1 |
| NM_139177.3 |
1027 |
Silent Mutation |
CCC,CCT |
P305P |
NP_631916.2 |
| XM_005257134.3 |
1027 |
Silent Mutation |
CCC,CCT |
P305P |
XP_005257191.1 |
| XM_006721754.3 |
1027 |
Silent Mutation |
CCC,CCT |
P312P |
XP_006721817.1 |
| XM_006721755.2 |
1027 |
Silent Mutation |
CCC,CCT |
P312P |
XP_006721818.1 |
| XM_006721756.2 |
1027 |
Intron |
|
|
XP_006721819.1 |
| XM_006721757.2 |
1027 |
Silent Mutation |
CCC,CCT |
P255P |
XP_006721820.1 |
| XM_006721758.3 |
1027 |
Intron |
|
|
XP_006721821.1 |
| XM_006721759.1 |
1027 |
Intron |
|
|
XP_006721822.1 |
| XM_011524493.1 |
1027 |
Silent Mutation |
CCC,CCT |
P312P |
XP_011522795.1 |
| XM_011524494.2 |
1027 |
Silent Mutation |
CCC,CCT |
P312P |
XP_011522796.1 |
| XM_011524495.2 |
1027 |
Intron |
|
|
XP_011522797.1 |
| XM_011524496.2 |
1027 |
Intron |
|
|
XP_011522798.1 |
| XM_011524498.2 |
1027 |
Intron |
|
|
XP_011522800.1 |
| XM_017024330.1 |
1027 |
Silent Mutation |
CCC,CCT |
P305P |
XP_016879819.1 |
| XM_017024331.1 |
1027 |
Silent Mutation |
CCC,CCT |
P305P |
XP_016879820.1 |
| XM_017024332.1 |
1027 |
Silent Mutation |
CCC,CCT |
P305P |
XP_016879821.1 |
| XM_017024333.1 |
1027 |
Silent Mutation |
CCC,CCT |
P262P |
XP_016879822.1 |
| XM_017024334.1 |
1027 |
Silent Mutation |
CCC,CCT |
P255P |
XP_016879823.1 |
| XM_017024335.1 |
1027 |
Silent Mutation |
CCC,CCT |
P248P |
XP_016879824.1 |
| XM_017024336.1 |
1027 |
Silent Mutation |
CCC,CCT |
P262P |
XP_016879825.1 |
| XM_017024337.1 |
1027 |
Silent Mutation |
CCC,CCT |
P262P |
XP_016879826.1 |
| XM_017024338.1 |
1027 |
Intron |
|
|
XP_016879827.1 |
| XM_017024339.1 |
1027 |
Intron |
|
|
XP_016879828.1 |
| XM_017024340.1 |
1027 |
Intron |
|
|
XP_016879829.1 |
| XM_017024341.1 |
1027 |
Intron |
|
|
XP_016879830.1 |
| XM_017024342.1 |
1027 |
Intron |
|
|
XP_016879831.1 |
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