Product Details
- SNP ID
-
rs141009211
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
12
- Location
-
Chr.1:1754585 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TGCTTCCCGACATCCATGTCCAGGC[C/T]TGCAGCCTGCGAGCCGTTCTCACCC
- Phenotype
-
MIM: 611616
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
NADK
PubMed Links
Gene Details
- Gene
- NADK
- Gene Name
- NAD kinase
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001198993.1 |
728 |
Missense Mutation |
AGC,GGC |
S268G |
NP_001185922.1 |
NM_001198994.1 |
728 |
Missense Mutation |
AGC,GGC |
S413G |
NP_001185923.1 |
NM_001198995.1 |
728 |
Missense Mutation |
AGC,GGC |
S236G |
NP_001185924.1 |
NM_023018.4 |
728 |
Missense Mutation |
AGC,GGC |
S268G |
NP_075394.3 |
XM_005244778.2 |
728 |
Missense Mutation |
AGC,GGC |
S268G |
XP_005244835.1 |
XM_006710837.2 |
728 |
Missense Mutation |
AGC,GGC |
S268G |
XP_006710900.1 |
XM_006710838.2 |
728 |
Missense Mutation |
AGC,GGC |
S181G |
XP_006710901.1 |
XM_006710839.1 |
728 |
Missense Mutation |
AGC,GGC |
S372G |
XP_006710902.1 |
XM_011542006.1 |
728 |
Missense Mutation |
AGC,GGC |
S165G |
XP_011540308.1 |
XM_011542007.1 |
728 |
Missense Mutation |
AGC,GGC |
S165G |
XP_011540309.1 |
XM_011542008.1 |
728 |
Missense Mutation |
AGC,GGC |
S165G |
XP_011540310.1 |
XM_011542009.2 |
728 |
Missense Mutation |
AGC,GGC |
S165G |
XP_011540311.1 |
XM_017002143.1 |
728 |
Missense Mutation |
AGC,GGC |
S268G |
XP_016857632.1 |
XM_017002144.1 |
728 |
Missense Mutation |
AGC,GGC |
S156G |
XP_016857633.1 |
XM_017002145.1 |
728 |
Missense Mutation |
AGC,GGC |
S146G |
XP_016857634.1 |
XM_017002146.1 |
728 |
Missense Mutation |
AGC,GGC |
S146G |
XP_016857635.1 |
- Gene
- SLC35E2
- Gene Name
- solute carrier family 35 member E2
There are no transcripts associated with this gene.
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