Product Details
- SNP ID
-
rs200731719
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.9:17135278 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CAGGGGGCCGGCGAGGGCCTGGGGG[G/T]GCAGCTCCGGCTCATGCTCCCCTCC
- Phenotype
-
MIM: 611870
- Polymorphism
- G/T, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
CNTLN
PubMed Links
Gene Details
- Gene
- CNTLN
- Gene Name
- centlein
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001114395.2 |
288 |
Silent Mutation |
GGG,GGT |
G71G |
NP_001107867.1 |
NM_001286984.1 |
288 |
Silent Mutation |
GGG,GGT |
G71G |
NP_001273913.1 |
NM_001286985.1 |
288 |
Intron |
|
|
NP_001273914.1 |
NM_017738.3 |
288 |
Silent Mutation |
GGG,GGT |
G71G |
NP_060208.2 |
XM_005251492.1 |
288 |
Silent Mutation |
GGG,GGT |
G71G |
XP_005251549.1 |
XM_006716793.3 |
288 |
Intron |
|
|
XP_006716856.1 |
XM_011517941.2 |
288 |
Silent Mutation |
GGG,GGT |
G71G |
XP_011516243.1 |
XM_017014839.1 |
288 |
Silent Mutation |
GGG,GGT |
G71G |
XP_016870328.1 |
XM_017014840.1 |
288 |
Silent Mutation |
GGG,GGT |
G71G |
XP_016870329.1 |
XM_017014841.1 |
288 |
Silent Mutation |
GGG,GGT |
G71G |
XP_016870330.1 |
XM_017014842.1 |
288 |
Silent Mutation |
GGG,GGT |
G71G |
XP_016870331.1 |
XM_017014843.1 |
288 |
Silent Mutation |
GGG,GGT |
G71G |
XP_016870332.1 |
XM_017014844.1 |
288 |
Intron |
|
|
XP_016870333.1 |
XM_017014845.1 |
288 |
Intron |
|
|
XP_016870334.1 |
XM_017014846.1 |
288 |
Intron |
|
|
XP_016870335.1 |
XM_017014847.1 |
288 |
Intron |
|
|
XP_016870336.1 |
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