Product Details
- SNP ID
-
rs7884685
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.X:145823920 on Build GRCh38
- Set Membership
-
HapMap
- Context Sequence [VIC/FAM]
- ATTTGGGGGGACGGCCCTAACCAGG[C/T]TGAATCTGAGAAACAACCATTTTTC
- Phenotype
-
MIM: 300561
MIM: 300565
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
SLITRK2
PubMed Links
Gene Details
- Gene
- SLITRK2
- Gene Name
- SLIT and NTRK like family member 2
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001144003.2 |
2938 |
Silent Mutation |
CTG,TTG |
L499L |
NP_001137475.1 |
NM_001144004.2 |
2938 |
Silent Mutation |
CTG,TTG |
L499L |
NP_001137476.1 |
NM_001144005.2 |
2938 |
Silent Mutation |
CTG,TTG |
L499L |
NP_001137477.1 |
NM_001144006.2 |
2938 |
Silent Mutation |
CTG,TTG |
L499L |
NP_001137478.1 |
NM_001144008.2 |
2938 |
Silent Mutation |
CTG,TTG |
L499L |
NP_001137480.1 |
NM_001144009.2 |
2938 |
Silent Mutation |
CTG,TTG |
L499L |
NP_001137481.1 |
NM_001144010.2 |
2938 |
Silent Mutation |
CTG,TTG |
L499L |
NP_001137482.1 |
NM_032539.4 |
2938 |
Silent Mutation |
CTG,TTG |
L499L |
NP_115928.1 |
XM_005262342.3 |
2938 |
Silent Mutation |
CTG,TTG |
L499L |
XP_005262399.1 |
XM_005262343.3 |
2938 |
Silent Mutation |
CTG,TTG |
L499L |
XP_005262400.1 |
XM_005262344.3 |
2938 |
Silent Mutation |
CTG,TTG |
L499L |
XP_005262401.1 |
XM_005262345.3 |
2938 |
Silent Mutation |
CTG,TTG |
L499L |
XP_005262402.1 |
- Gene
- TMEM257
- Gene Name
- transmembrane protein 257
There are no transcripts associated with this gene.
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