| 156083362 | CV2293037 | single nucleotide variant | NM_173852.4(KRTCAP2):c.-30G>A | not specified [RCV004148509] | uncertain significance | 1 | 155173254 | 155173254 | Human | | name |
| 155968222 | CV2391433 | single nucleotide variant | NM_173852.4(KRTCAP2):c.-72A>G | not specified [RCV004239828] | uncertain significance | 1 | 155173296 | 155173296 | Human | | name |
| 401748784 | CV2708347 | single nucleotide variant | NM_173852.4(KRTCAP2):c.-66A>G | not specified [RCV004313467] | uncertain significance | 1 | 155173290 | 155173290 | Human | | name |
| 405808276 | CV3266116 | single nucleotide variant | NM_173852.4(KRTCAP2):c.-35C>T | not specified [RCV004406998] | uncertain significance | 1 | 155173259 | 155173259 | Human | | name |
| 405808278 | CV3266117 | single nucleotide variant | NM_173852.4(KRTCAP2):c.-27G>A | not specified [RCV004406999] | likely benign | 1 | 155173251 | 155173251 | Human | | name |
| 407480708 | CV3455963 | single nucleotide variant | NM_173852.4(KRTCAP2):c.10G>A (p.Gly4Ser) | not specified [RCV004639785] | uncertain significance | 1 | 155172887 | 155172887 | Human | | name |
| 401888252 | CV2788201 | single nucleotide variant | NM_173852.4(KRTCAP2):c.197G>A (p.Gly66Glu) | not specified [RCV004352814] | uncertain significance | 1 | 155172591 | 155172591 | Human | | name |
| 598196601 | CV3991380 | single nucleotide variant | NM_173852.4(KRTCAP2):c.144C>A (p.Phe48Leu) | not specified [RCV005355209] | uncertain significance | 1 | 155172753 | 155172753 | Human | | name |
| 329380485 | CV2444413 | single nucleotide variant | NM_173852.4(KRTCAP2):c.373C>T (p.Pro125Ser) | not specified [RCV004263155] | uncertain significance | 1 | 155169478 | 155169478 | Human | | name |
| 329396229 | CV2462445 | single nucleotide variant | NM_173852.4(KRTCAP2):c.326A>G (p.Asn109Ser) | not specified [RCV004276636] | uncertain significance | 1 | 155169525 | 155169525 | Human | | name |
| 405808274 | CV3266115 | single nucleotide variant | NM_173852.4(KRTCAP2):c.307G>T (p.Val103Phe) | not specified [RCV004406997] | uncertain significance | 1 | 155169544 | 155169544 | Human | | name |
| 598222431 | CV3991379 | single nucleotide variant | NM_173852.4(KRTCAP2):c.362C>G (p.Pro121Arg) | not specified [RCV005360987] | uncertain significance | 1 | 155169489 | 155169489 | Human | | name |