Product Details
- SNP ID
-
rs199671668
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.11:66366203 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GACGGACAGGGTGACTGTGAAGACC[A/G]ACACAAGGCACAGCGCTGTCAGCCA
- Phenotype
-
MIM: 602110
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
LOC102724064
PubMed Links
Gene Details
- Gene
- LOC102724064
- Gene Name
- uncharacterized LOC102724064
There are no transcripts associated with this gene.
- Gene
- SLC29A2
- Gene Name
- solute carrier family 29 member 2
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_001300868.1 |
1276 |
Missense Mutation |
TCG,TTG |
S299L |
NP_001287797.1 |
| NM_001300869.1 |
1276 |
Silent Mutation |
GTC,GTT |
V254V |
NP_001287798.1 |
| NM_001532.2 |
1276 |
Missense Mutation |
TCG,TTG |
S299L |
NP_001523.2 |
| XM_011544974.1 |
1276 |
Silent Mutation |
GTC,GTT |
V365V |
XP_011543276.1 |
| XM_017017630.1 |
1276 |
Silent Mutation |
GTC,GTT |
V365V |
XP_016873119.1 |
| XM_017017631.1 |
1276 |
Missense Mutation |
TCG,TTG |
S299L |
XP_016873120.1 |
| XM_017017632.1 |
1276 |
Missense Mutation |
TCG,TTG |
S299L |
XP_016873121.1 |
| XM_017017633.1 |
1276 |
Silent Mutation |
GTC,GTT |
V365V |
XP_016873122.1 |
| XM_017017634.1 |
1276 |
Intron |
|
|
XP_016873123.1 |
| XM_017017635.1 |
1276 |
Intron |
|
|
XP_016873124.1 |
| XM_017017636.1 |
1276 |
Missense Mutation |
TCG,TTG |
S299L |
XP_016873125.1 |
| XM_017017637.1 |
1276 |
Silent Mutation |
GTC,GTT |
V254V |
XP_016873126.1 |
| XM_017017638.1 |
1276 |
Silent Mutation |
GTC,GTT |
V245V |
XP_016873127.1 |
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