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CTCCTCCTGCTGCTGCTGCTGAGCT[C/T]GGGACTCAGTGGGACCCAGGACTGC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 613358 MIM: 600007 | ||||||||||||||||||||
Literature Links: |
ALDH16A1 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
ALDH16A1 - aldehyde dehydrogenase 16 family member A1 | ||||||
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There are no transcripts associated with this gene. |
FLT3LG - fms related tyrosine kinase 3 ligand | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001204502.1 | 211 | Missense Mutation | TCG,TTG | S,L 22 | NP_001191431.1 | |
NM_001204503.1 | 211 | Missense Mutation | TCG,TTG | S,L 22 | NP_001191432.1 | |
NM_001278637.1 | 211 | UTR 5 | NP_001265566.1 | |||
NM_001278638.1 | 211 | UTR 5 | NP_001265567.1 | |||
NM_001459.3 | 211 | Missense Mutation | TCG,TTG | S,L 22 | NP_001450.2 | |
XM_005258680.4 | 211 | Missense Mutation | TCG,TTG | S,L 22 | XP_005258737.3 | |
XM_005258681.4 | 211 | Missense Mutation | TCG,TTG | S,L 22 | XP_005258738.3 | |
XM_005258682.4 | 211 | Missense Mutation | TCG,TTG | S,L 22 | XP_005258739.3 | |
XM_005258683.4 | 211 | Missense Mutation | TCG,TTG | S,L 22 | XP_005258740.3 | |
XM_006723116.3 | 211 | Missense Mutation | TCG,TTG | S,L 22 | XP_006723179.2 | |
XM_011526675.2 | 211 | Missense Mutation | TCG,TTG | S,L 22 | XP_011524977.1 | |
XM_011526676.2 | 211 | Missense Mutation | TCG,TTG | S,L 22 | XP_011524978.1 | |
XM_011526677.2 | 211 | Missense Mutation | TCG,TTG | S,L 22 | XP_011524979.1 | |
XM_011526678.2 | 211 | Missense Mutation | TCG,TTG | S,L 22 | XP_011524980.1 | |
XM_011526680.2 | 211 | Missense Mutation | TCG,TTG | S,L 22 | XP_011524982.1 | |
XM_011526682.2 | 211 | UTR 5 | XP_011524984.1 | |||
XM_017026532.1 | 211 | Missense Mutation | TCG,TTG | S,L 22 | XP_016882021.1 | |
XM_017026533.1 | 211 | Intron | XP_016882022.1 | |||
XM_017026534.1 | 211 | Intron | XP_016882023.1 | |||
XM_017026535.1 | 211 | UTR 5 | XP_016882024.1 |