| 8654050 | CV130625 | single nucleotide variant | NM_014620.5(HOXC4):c.-123-12551C>A | Lung cancer [RCV000111112] | uncertain significance | 12 | 54040609 | 54040609 | Human | | name |
| 407528101 | CV3433825 | single nucleotide variant | NM_153633.3(HOXC4):c.14C>G (p.Ser5Trp) | not specified [RCV004633026] | uncertain significance | 12 | 54053936 | 54053936 | Human | | name |
| 156190679 | CV2289283 | single nucleotide variant | NM_153633.3(HOXC4):c.83A>G (p.Tyr28Cys) | not specified [RCV004152265] | uncertain significance | 12 | 54054005 | 54054005 | Human | | name |
| 329370774 | CV2461857 | single nucleotide variant | NM_153633.3(HOXC4):c.77A>G (p.Asn26Ser) | not specified [RCV004271769] | uncertain significance | 12 | 54053999 | 54053999 | Human | | name |
| 401932187 | CV2807059 | single nucleotide variant | NM_153633.3(HOXC4):c.369C>T (p.Asp123=) | not provided [RCV003391863] | likely benign | 12 | 54054291 | 54054291 | Human | | name |
| 401932189 | CV2807060 | single nucleotide variant | NM_153633.3(HOXC4):c.387C>A (p.Ala129=) | not provided [RCV003391864] | likely benign | 12 | 54054309 | 54054309 | Human | | name |
| 156148013 | CV2292623 | single nucleotide variant | NM_153633.3(HOXC4):c.284A>G (p.Gln95Arg) | not specified [RCV004154313] | uncertain significance | 12 | 54054206 | 54054206 | Human | | name |
| 156164573 | CV2319718 | single nucleotide variant | NM_153633.3(HOXC4):c.257C>T (p.Ala86Val) | not specified [RCV004187255] | uncertain significance | 12 | 54054179 | 54054179 | Human | | name |
| 405797912 | CV3263425 | single nucleotide variant | NM_153633.3(HOXC4):c.271C>T (p.Pro91Ser) | not specified [RCV004402064] | uncertain significance | 12 | 54054193 | 54054193 | Human | | name |
| 597772686 | CV3679719 | single nucleotide variant | NM_153633.3(HOXC4):c.164C>G (p.Pro55Arg) | not specified [RCV004928731] | uncertain significance | 12 | 54054086 | 54054086 | Human | | name |
| 156072533 | CV2325337 | single nucleotide variant | NM_153633.3(HOXC4):c.692C>A (p.Ala231Glu) | not specified [RCV004177719] | uncertain significance | 12 | 54055102 | 54055102 | Human | | name |
| 401864775 | CV2778038 | single nucleotide variant | NM_153633.3(HOXC4):c.643C>A (p.His215Asn) | not specified [RCV004347992] | uncertain significance | 12 | 54055053 | 54055053 | Human | | name |
| 405798287 | CV3263427 | single nucleotide variant | NM_153633.3(HOXC4):c.653C>T (p.Pro218Leu) | not specified [RCV004402066] | uncertain significance | 12 | 54055063 | 54055063 | Human | | name |
| 405798282 | CV3263428 | single nucleotide variant | NM_153633.3(HOXC4):c.676C>A (p.Pro226Thr) | not specified [RCV004402067] | uncertain significance | 12 | 54055086 | 54055086 | Human | | name |
| 405798277 | CV3263429 | single nucleotide variant | NM_153633.3(HOXC4):c.748G>A (p.Ala250Thr) | not specified [RCV004402068] | uncertain significance | 12 | 54055158 | 54055158 | Human | | name |
| 405798273 | CV3263430 | single nucleotide variant | NM_153633.3(HOXC4):c.764A>G (p.Gln255Arg) | not specified [RCV004402069] | uncertain significance | 12 | 54055174 | 54055174 | Human | | name |
| 597772692 | CV3679720 | single nucleotide variant | NM_153633.3(HOXC4):c.299C>T (p.Pro100Leu) | not specified [RCV004928732] | uncertain significance | 12 | 54054221 | 54054221 | Human | | name |
| 597772695 | CV3679721 | single nucleotide variant | NM_153633.3(HOXC4):c.755C>T (p.Pro252Leu) | not specified [RCV004928733] | uncertain significance | 12 | 54055165 | 54055165 | Human | | name |
| 597772699 | CV3679722 | single nucleotide variant | NM_153633.3(HOXC4):c.322G>T (p.Ala108Ser) | not specified [RCV004928734] | uncertain significance | 12 | 54054244 | 54054244 | Human | | name |
| 598192012 | CV3971778 | single nucleotide variant | NM_153633.3(HOXC4):c.785C>T (p.Thr262Ile) | not specified [RCV005354380] | uncertain significance | 12 | 54055195 | 54055195 | Human | | name |
| 598192019 | CV3971779 | single nucleotide variant | NM_153633.3(HOXC4):c.718C>G (p.Pro240Ala) | not specified [RCV005354381] | uncertain significance | 12 | 54055128 | 54055128 | Human | | name |
| 598249266 | CV3971780 | single nucleotide variant | NM_153633.3(HOXC4):c.591G>C (p.Glu197Asp) | not specified [RCV005345562] | uncertain significance | 12 | 54055001 | 54055001 | Human | | name |
| 598249274 | CV3971781 | single nucleotide variant | NM_153633.3(HOXC4):c.491C>A (p.Thr164Asn) | not specified [RCV005345563] | uncertain significance | 12 | 54054901 | 54054901 | Human | | name |