| 405802013 | CV3272000 | single nucleotide variant | NM_007044.4(KATNA1):c.27T>A (p.Asn9Lys) | not specified [RCV004403698] | uncertain significance | 6 | 149638521 | 149638521 | Human | | name |
| 156240658 | CV2350358 | single nucleotide variant | NM_007044.4(KATNA1):c.41G>A (p.Arg14His) | not specified [RCV004202303] | uncertain significance | 6 | 149638507 | 149638507 | Human | | name |
| 401758975 | CV2705297 | single nucleotide variant | NM_007044.4(KATNA1):c.71C>T (p.Ser24Phe) | not specified [RCV004311985] | uncertain significance | 6 | 149638477 | 149638477 | Human | | name |
| 401779467 | CV2718567 | single nucleotide variant | NM_007044.4(KATNA1):c.65A>G (p.Tyr22Cys) | not specified [RCV004318366] | uncertain significance | 6 | 149638483 | 149638483 | Human | | name |
| 597786611 | CV3690868 | single nucleotide variant | NM_007044.4(KATNA1):c.40C>T (p.Arg14Cys) | not specified [RCV004932298] | uncertain significance | 6 | 149638508 | 149638508 | Human | | name |
| 598234212 | CV3980003 | single nucleotide variant | NM_007044.4(KATNA1):c.29T>C (p.Val10Ala) | not specified [RCV005363479] | uncertain significance | 6 | 149638519 | 149638519 | Human | | name |
| 156335216 | CV2333496 | single nucleotide variant | NM_007044.4(KATNA1):c.254C>T (p.Ala85Val) | not specified [RCV004190191] | uncertain significance | 6 | 149632825 | 149632825 | Human | | name |
| 329371030 | CV2461923 | single nucleotide variant | NM_007044.4(KATNA1):c.253G>C (p.Ala85Pro) | not specified [RCV004271828] | uncertain significance | 6 | 149632826 | 149632826 | Human | | name |
| 405802017 | CV3272002 | single nucleotide variant | NM_007044.4(KATNA1):c.286G>A (p.Glu96Lys) | not specified [RCV004403700] | uncertain significance | 6 | 149632793 | 149632793 | Human | | name |
| 156401239 | CV2210740 | single nucleotide variant | NM_007044.4(KATNA1):c.383A>G (p.Asn128Ser) | not specified [RCV004085838] | uncertain significance | 6 | 149623221 | 149623221 | Human | | name |
| 156298384 | CV2251946 | single nucleotide variant | NM_007044.4(KATNA1):c.436A>G (p.Asn146Asp) | not specified [RCV004119912] | uncertain significance | 6 | 149623168 | 149623168 | Human | | name |
| 156066295 | CV2349008 | single nucleotide variant | NM_007044.4(KATNA1):c.791C>T (p.Thr264Ile) | not specified [RCV004203434] | uncertain significance | 6 | 149601691 | 149601691 | Human | | name |
| 156097307 | CV2399184 | single nucleotide variant | NM_007044.4(KATNA1):c.872G>A (p.Arg291His) | not specified [RCV004246614] | uncertain significance | 6 | 149601610 | 149601610 | Human | | name |
| 329355447 | CV2445437 | single nucleotide variant | NM_007044.4(KATNA1):c.319A>G (p.Arg107Gly) | not specified [RCV004257499] | uncertain significance | 6 | 149632760 | 149632760 | Human | | name |
| 401742646 | CV2715283 | single nucleotide variant | NM_007044.4(KATNA1):c.550A>G (p.Ser184Gly) | not specified [RCV004324622] | uncertain significance | 6 | 149604734 | 149604734 | Human | | name |
| 401767464 | CV2727172 | single nucleotide variant | NM_007044.4(KATNA1):c.655A>C (p.Lys219Gln) | not specified [RCV004325526] | uncertain significance | 6 | 149603342 | 149603342 | Human | | name |
| 401893351 | CV2756620 | single nucleotide variant | NM_007044.4(KATNA1):c.515C>T (p.Ala172Val) | not specified [RCV004345141] | uncertain significance | 6 | 149604769 | 149604769 | Human | | name |
| 405802019 | CV3272003 | single nucleotide variant | NM_007044.4(KATNA1):c.388C>T (p.Pro130Ser) | not specified [RCV004403701] | uncertain significance | 6 | 149623216 | 149623216 | Human | | name |
| 405802022 | CV3272004 | single nucleotide variant | NM_007044.4(KATNA1):c.649G>C (p.Ala217Pro) | not specified [RCV004403702] | uncertain significance | 6 | 149603348 | 149603348 | Human | | name |
| 405802026 | CV3272006 | single nucleotide variant | NM_007044.4(KATNA1):c.708G>T (p.Lys236Asn) | not specified [RCV004403704] | uncertain significance | 6 | 149603289 | 149603289 | Human | | name |
| 405802028 | CV3272007 | single nucleotide variant | NM_007044.4(KATNA1):c.745G>A (p.Gly249Ser) | not specified [RCV004403705] | uncertain significance | 6 | 149601737 | 149601737 | Human | | name |
| 405802030 | CV3272008 | single nucleotide variant | NM_007044.4(KATNA1):c.890C>G (p.Ala297Gly) | not specified [RCV004403706] | uncertain significance | 6 | 149598349 | 149598349 | Human | | name |
| 407467625 | CV3448330 | single nucleotide variant | NM_007044.4(KATNA1):c.386G>A (p.Arg129His) | not specified [RCV004635948] | uncertain significance | 6 | 149623218 | 149623218 | Human | | name |
| 407467628 | CV3448331 | single nucleotide variant | NM_007044.4(KATNA1):c.457C>T (p.Arg153Cys) | not specified [RCV004635949] | uncertain significance | 6 | 149623147 | 149623147 | Human | | name |
| 597786600 | CV3690865 | single nucleotide variant | NM_007044.4(KATNA1):c.458G>A (p.Arg153His) | not specified [RCV004932295] | uncertain significance | 6 | 149623146 | 149623146 | Human | | name |
| 597786604 | CV3690866 | single nucleotide variant | NM_007044.4(KATNA1):c.343C>T (p.Arg115Cys) | not specified [RCV004932296] | uncertain significance | 6 | 149623261 | 149623261 | Human | | name |
| 597786614 | CV3690869 | single nucleotide variant | NM_007044.4(KATNA1):c.673G>A (p.Val225Ile) | not specified [RCV004932299] | uncertain significance | 6 | 149603324 | 149603324 | Human | | name |
| 598259139 | CV3980002 | single nucleotide variant | NM_007044.4(KATNA1):c.404G>C (p.Arg135Thr) | not specified [RCV005347356] | uncertain significance | 6 | 149623200 | 149623200 | Human | | name |
| 8631872 | CV87078 | single nucleotide variant | NM_007044.3(KATNA1):c.722C>T (p.Pro241Leu) | Malignant melanoma [RCV000067169] | not provided | 6 | 149603275 | 149603275 | Human | | name |
| 8631873 | CV87079 | single nucleotide variant | NM_007044.3(KATNA1):c.721C>T (p.Pro241Ser) | Malignant melanoma [RCV000067170] | not provided | 6 | 149603276 | 149603276 | Human | | name |
| 156049966 | CV2304545 | single nucleotide variant | NM_007044.4(KATNA1):c.1131C>G (p.Ile377Met) | not specified [RCV004164623] | uncertain significance | 6 | 149597526 | 149597526 | Human | | name |
| 156056248 | CV2320599 | single nucleotide variant | NM_007044.4(KATNA1):c.1458T>G (p.Phe486Leu) | not specified [RCV004172219] | uncertain significance | 6 | 149595054 | 149595054 | Human | | name |
| 405802009 | CV3271998 | single nucleotide variant | NM_007044.4(KATNA1):c.1177A>G (p.Ile393Val) | not specified [RCV004403696] | uncertain significance | 6 | 149597163 | 149597163 | Human | | name |
| 405802011 | CV3271999 | single nucleotide variant | NM_007044.4(KATNA1):c.1217T>C (p.Leu406Pro) | not specified [RCV004403697] | uncertain significance | 6 | 149597123 | 149597123 | Human | | name |
| 407467622 | CV3448329 | single nucleotide variant | NM_007044.4(KATNA1):c.1283C>G (p.Ala428Gly) | not specified [RCV004635947] | uncertain significance | 6 | 149595229 | 149595229 | Human | | name |
| 597786618 | CV3690870 | single nucleotide variant | NM_007044.4(KATNA1):c.1448A>G (p.Lys483Arg) | not specified [RCV004932300] | uncertain significance | 6 | 149595064 | 149595064 | Human | | name |
| 598234220 | CV3980004 | single nucleotide variant | NM_007044.4(KATNA1):c.1091A>C (p.Asp364Ala) | not specified [RCV005363480] | uncertain significance | 6 | 149597566 | 149597566 | Human | | name |
| 598259143 | CV3980005 | single nucleotide variant | NM_007044.4(KATNA1):c.1337G>A (p.Arg446Gln) | not specified [RCV005347357] | uncertain significance | 6 | 149595175 | 149595175 | Human | | name |
| 598234226 | CV3980006 | single nucleotide variant | NM_007044.4(KATNA1):c.1216C>T (p.Leu406Phe) | not specified [RCV005363481] | uncertain significance | 6 | 149597124 | 149597124 | Human | | name |
| 598234232 | CV3980007 | single nucleotide variant | NM_007044.4(KATNA1):c.1175G>A (p.Arg392Gln) | not specified [RCV005363482] | uncertain significance | 6 | 149597165 | 149597165 | Human | | name |
| 598234238 | CV3980008 | single nucleotide variant | NM_007044.4(KATNA1):c.1173A>C (p.Leu391Phe) | not specified [RCV005363483] | uncertain significance | 6 | 149597167 | 149597167 | Human | | name |