Product Details

SNP ID
rs79620092
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.5:180603322 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCCTCCTCGGGCCCCCCGCTCAGGC[C/T]GCCGCCGCCTCCCTTGGGAGTCAGG
Phenotype
MIM: 136352
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
FLT4 PubMed Links

Gene Details

Gene
FLT4
Gene Name
fms related tyrosine kinase 4
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_002020.4 4498 Intron NP_002011.2
NM_182925.4 4498 Missense Mutation NP_891555.2
XM_011534478.2 4498 Missense Mutation XP_011532780.1
XM_011534484.2 4498 Missense Mutation XP_011532786.1
XM_017009263.1 4498 UTR 3 XP_016864752.1
XM_017009264.1 4498 Intron XP_016864753.1
XM_017009265.1 4498 Intron XP_016864754.1
XM_017009266.1 4498 Intron XP_016864755.1
XM_017009267.1 4498 Intron XP_016864756.1
XM_017009268.1 4498 Missense Mutation XP_016864757.1

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