Product Details
- SNP ID
-
rs17199
- Assay Type
- Validated
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.7:15612145 on Build GRCh38
- Set Membership
-
HapMap
Validated
- Context Sequence [VIC/FAM]
- ACATACCTGCTCACTGCCATACGCA[C/T]GACCAAACACATCTGGAATATTCAA
- Phenotype
-
MIM: 600535
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
MEOX2
PubMed Links
Gene Details
- Gene
- MEOX2
- Gene Name
- mesenchyme homeobox 2
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_005924.4 |
1438 |
UTR 3 |
|
|
NP_005915.2 |
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