| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | FLT1, LOC130009458 (E345G) | Single nucleotide variant (missense variant) | not specified | |
| | FLT1, LOC126861720 (M945T) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (intron variant) | Squamous cell carcinoma | |
| | | Single nucleotide variant (intron variant) | Lung adenocarcinoma | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | FLT1, LOC126861720 (G988S) | Single nucleotide variant (missense variant) | not specified | |
| | FLT1, LOC130009458 (Q341R) | Single nucleotide variant (missense variant) | not specified | |
| | FLT1, LOC126861720 (M938V) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Carcinoma of colon | |
| | | Single nucleotide variant (synonymous variant) | Carcinoma of colon | |
| | | Single nucleotide variant (synonymous variant) | Carcinoma of colon | |
| | | Insertion (frameshift variant) | Carcinoma of colon | |
| | | Single nucleotide variant (intron variant) | Carcinoma of colon | |
| | | Single nucleotide variant (intron variant) | Carcinoma of colon | |
| | FLT1, LOC126861720 (S1015fs) | Insertion (frameshift variant) | Carcinoma of colon | |
| | | Single nucleotide variant (intron variant) | Carcinoma of colon | |
| | | Single nucleotide variant (intron variant) | Carcinoma of colon | |
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