Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 136352 | ||||||||||||||||||||
Literature Links: |
FLT4 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
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 |
FLT4 - fms related tyrosine kinase 4 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_002020.4 | 4507 | Intron | NP_002011.2 | |||
NM_182925.4 | 4507 | Missense Mutation | CAG,CCG | Q,P 1324 | NP_891555.2 | |
XM_011534478.2 | 4507 | Missense Mutation | CAG,CCG | Q,P 1401 | XP_011532780.1 | |
XM_011534484.2 | 4507 | Missense Mutation | CAG,CCG | Q,P 1171 | XP_011532786.1 | |
XM_017009263.1 | 4507 | UTR 3 | XP_016864752.1 | |||
XM_017009264.1 | 4507 | Intron | XP_016864753.1 | |||
XM_017009265.1 | 4507 | Intron | XP_016864754.1 | |||
XM_017009266.1 | 4507 | Intron | XP_016864755.1 | |||
XM_017009267.1 | 4507 | Intron | XP_016864756.1 | |||
XM_017009268.1 | 4507 | Missense Mutation | CAG,CCG | Q,P 1298 | XP_016864757.1 |