Product Details
- SNP ID
-
rs61737308
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.15:77614797 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- ACAGGAGCCGACAGTCGCAGGCCAG[C/T]GGGTTGGAGTCCAGGATGAGTGTCT
- Phenotype
-
MIM: 609791
- Polymorphism
- C/T, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
LINGO1
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs3743481] are located under a probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.
Gene Details
- Gene
- LINGO1
- Gene Name
- leucine rich repeat and Ig domain containing 1
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_001301186.1 |
1304 |
Silent Mutation |
CCC,CCT |
P364P |
NP_001288115.1 |
| NM_001301187.1 |
1304 |
Silent Mutation |
CCC,CCT |
P364P |
NP_001288116.1 |
| NM_001301189.1 |
1304 |
Silent Mutation |
CCC,CCT |
P364P |
NP_001288118.1 |
| NM_001301191.1 |
1304 |
Silent Mutation |
CCC,CCT |
P364P |
NP_001288120.1 |
| NM_001301192.1 |
1304 |
Silent Mutation |
CCC,CCT |
P364P |
NP_001288121.1 |
| NM_001301194.1 |
1304 |
Silent Mutation |
CCC,CCT |
P364P |
NP_001288123.1 |
| NM_001301195.1 |
1304 |
Silent Mutation |
CCC,CCT |
P364P |
NP_001288124.1 |
| NM_001301197.1 |
1304 |
Silent Mutation |
CCC,CCT |
P364P |
NP_001288126.1 |
| NM_001301198.1 |
1304 |
Silent Mutation |
CCC,CCT |
P364P |
NP_001288127.1 |
| NM_001301199.1 |
1304 |
Silent Mutation |
CCC,CCT |
P364P |
NP_001288128.1 |
| NM_001301200.1 |
1304 |
Silent Mutation |
CCC,CCT |
P364P |
NP_001288129.1 |
| NM_032808.6 |
1304 |
Silent Mutation |
CCC,CCT |
P370P |
NP_116197.4 |
| XM_011522118.2 |
1304 |
Silent Mutation |
|
|
XP_011520420.1 |
| XM_017022682.1 |
1304 |
Silent Mutation |
|
|
XP_016878171.1 |
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