Product Details
- SNP ID
-
rs184068804
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.6:8413603 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TTCTTGCTTCCACTGATTTGTTTAT[C/G]AAATCATACAGTGATGGTAGTCTTA
- Phenotype
-
MIM: 610845
- Polymorphism
- C/G, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
SLC35B3
PubMed Links
Gene Details
- Gene
- SLC35B3
- Gene Name
- solute carrier family 35 member B3
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001142541.2 |
1373 |
Missense Mutation |
TTC,TTG |
F384L |
NP_001136013.1 |
NM_015948.4 |
1373 |
Missense Mutation |
TTC,TTG |
F384L |
NP_057032.2 |
XM_005249156.3 |
1373 |
Missense Mutation |
TTC,TTG |
F386L |
XP_005249213.1 |
XM_005249157.2 |
1373 |
Missense Mutation |
TTC,TTG |
F384L |
XP_005249214.1 |
XM_005249158.1 |
1373 |
Missense Mutation |
TTC,TTG |
F352L |
XP_005249215.1 |
XM_006715102.3 |
1373 |
Missense Mutation |
TTC,TTG |
F384L |
XP_006715165.1 |
XM_006715103.3 |
1373 |
Missense Mutation |
TTC,TTG |
F355L |
XP_006715166.1 |
XM_011514648.1 |
1373 |
Missense Mutation |
TTC,TTG |
F352L |
XP_011512950.1 |
XM_011514650.2 |
1373 |
Intron |
|
|
XP_011512952.1 |
XM_017010910.1 |
1373 |
Missense Mutation |
TTC,TTG |
F384L |
XP_016866399.1 |
XM_017010911.1 |
1373 |
Missense Mutation |
TTC,TTG |
F384L |
XP_016866400.1 |
XM_017010912.1 |
1373 |
Missense Mutation |
TTC,TTG |
F353L |
XP_016866401.1 |
XM_017010913.1 |
1373 |
Missense Mutation |
TTC,TTG |
F353L |
XP_016866402.1 |
XM_017010914.1 |
1373 |
Missense Mutation |
TTC,TTG |
F352L |
XP_016866403.1 |
XM_017010915.1 |
1373 |
Missense Mutation |
TTC,TTG |
F321L |
XP_016866404.1 |
View Full Product Details