Product Details
- SNP ID
-
rs112498405
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.12:104805232 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- AAGGCTAACAGAGCTGTCCCGAGCA[A/G]ATCACCCAATGCTGTTAGGTAGGGG
- Phenotype
-
MIM: 610802
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
SLC41A2
PubMed Links
Gene Details
- Gene
- SLC41A2
- Gene Name
- solute carrier family 41 member 2
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_032148.3 |
2170 |
Silent Mutation |
CTG,TTG |
L548L |
NP_115524.3 |
XM_005269176.1 |
2170 |
Silent Mutation |
CTG,TTG |
L548L |
XP_005269233.1 |
XM_005269178.1 |
2170 |
Silent Mutation |
CTG,TTG |
L548L |
XP_005269235.1 |
XM_005269179.1 |
2170 |
Silent Mutation |
CTG,TTG |
L548L |
XP_005269236.1 |
XM_006719630.2 |
2170 |
Silent Mutation |
CTG,TTG |
L548L |
XP_006719693.1 |
XM_011538807.2 |
2170 |
Silent Mutation |
CTG,TTG |
L548L |
XP_011537109.1 |
XM_011538808.1 |
2170 |
Silent Mutation |
CTG,TTG |
L548L |
XP_011537110.1 |
XM_011538809.1 |
2170 |
Silent Mutation |
CTG,TTG |
L548L |
XP_011537111.1 |
XM_011538810.2 |
2170 |
Silent Mutation |
CTG,TTG |
L548L |
XP_011537112.1 |
XM_011538811.2 |
2170 |
Silent Mutation |
CTG,TTG |
L548L |
XP_011537113.1 |
XM_011538813.2 |
2170 |
Silent Mutation |
CTG,TTG |
L322L |
XP_011537115.1 |
XM_017020013.1 |
2170 |
Silent Mutation |
CTG,TTG |
L548L |
XP_016875502.1 |
XM_017020014.1 |
2170 |
UTR 3 |
|
|
XP_016875503.1 |
XM_017020015.1 |
2170 |
Intron |
|
|
XP_016875504.1 |
XM_017020016.1 |
2170 |
Silent Mutation |
CTG,TTG |
L337L |
XP_016875505.1 |
XM_017020017.1 |
2170 |
Silent Mutation |
CTG,TTG |
L336L |
XP_016875506.1 |
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