Product Details
- SNP ID
-
rs118203959
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.15:74180121 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TTGGCACCCAACAGGGCCGTCTTGC[G/A]GAAGACCTGCAGGGTTGGGTTGTGC
- Phenotype
-
MIM: 602059
MIM: 610745
- Polymorphism
- G/A, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
ISLR
PubMed Links
Gene Details
- Gene
- ISLR
- Gene Name
- immunoglobulin superfamily containing leucine rich repeat
There are no transcripts associated with this gene.
- Gene
- STRA6
- Gene Name
- stimulated by retinoic acid 6
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_001142617.1 |
2175 |
Missense Mutation |
CGC,TGC |
R655C |
NP_001136089.1 |
| NM_001142618.1 |
2175 |
Missense Mutation |
CGC,TGC |
R655C |
NP_001136090.1 |
| NM_001142619.1 |
2175 |
Missense Mutation |
CGC,TGC |
R646C |
NP_001136091.1 |
| NM_001142620.1 |
2175 |
Intron |
|
|
NP_001136092.1 |
| NM_001199040.1 |
2175 |
Missense Mutation |
CGC,TGC |
R692C |
NP_001185969.1 |
| NM_001199041.1 |
2175 |
Missense Mutation |
CGC,TGC |
R670C |
NP_001185970.1 |
| NM_001199042.1 |
2175 |
Missense Mutation |
CGC,TGC |
R694C |
NP_001185971.1 |
| NM_022369.3 |
2175 |
Missense Mutation |
CGC,TGC |
R655C |
NP_071764.3 |
| XM_011521883.1 |
2175 |
Missense Mutation |
CGC,TGC |
R655C |
XP_011520185.1 |
| XM_011521884.1 |
2175 |
Missense Mutation |
CGC,TGC |
R592C |
XP_011520186.1 |
| XM_011521885.2 |
2175 |
Intron |
|
|
XP_011520187.1 |
| XM_017022478.1 |
2175 |
Missense Mutation |
CGC,TGC |
R671C |
XP_016877967.1 |
| XM_017022479.1 |
2175 |
Missense Mutation |
CGC,TGC |
R655C |
XP_016877968.1 |
| XM_017022480.1 |
2175 |
Missense Mutation |
CGC,TGC |
R592C |
XP_016877969.1 |
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