| 329378507 | CV2459827 | single nucleotide variant | NM_014505.6(KCNMB4):c.23A>C (p.Tyr8Ser) | not specified [RCV004279328] | uncertain significance | 12 | 70366757 | 70366757 | Human | | name |
| 329378097 | CV2460678 | single nucleotide variant | NM_014505.6(KCNMB4):c.16G>T (p.Val6Leu) | not specified [RCV004271026] | uncertain significance | 12 | 70366750 | 70366750 | Human | | name |
| 156280325 | CV2348438 | single nucleotide variant | NM_014505.6(KCNMB4):c.76A>G (p.Ile26Val) | not specified [RCV004193628] | uncertain significance | 12 | 70366810 | 70366810 | Human | | name |
| 597767249 | CV3694723 | single nucleotide variant | NM_014505.6(KCNMB4):c.128C>T (p.Ala43Val) | not specified [RCV004927244] | uncertain significance | 12 | 70366862 | 70366862 | Human | | name |
| 155962693 | CV2197629 | single nucleotide variant | NM_014505.6(KCNMB4):c.440C>T (p.Thr147Ile) | not specified [RCV004074845] | uncertain significance | 12 | 70400312 | 70400312 | Human | | name |
| 156241557 | CV2265776 | single nucleotide variant | NM_014505.6(KCNMB4):c.620G>A (p.Arg207His) | not specified [RCV004126397] | uncertain significance | 12 | 70430640 | 70430640 | Human | | name |
| 156001521 | CV2378822 | single nucleotide variant | NM_014505.6(KCNMB4):c.553G>T (p.Val185Phe) | not specified [RCV004231266] | uncertain significance | 12 | 70430573 | 70430573 | Human | | name |
| 401867867 | CV2767100 | single nucleotide variant | NM_014505.6(KCNMB4):c.574A>G (p.Ile192Val) | not specified [RCV004347501] | uncertain significance | 12 | 70430594 | 70430594 | Human | | name |
| 401871013 | CV2788985 | single nucleotide variant | NM_014505.6(KCNMB4):c.585G>T (p.Lys195Asn) | not specified [RCV004363299] | uncertain significance | 12 | 70430605 | 70430605 | Human | | name |
| 405806996 | CV3264984 | single nucleotide variant | NM_014505.6(KCNMB4):c.619C>T (p.Arg207Cys) | not specified [RCV004406332] | uncertain significance | 12 | 70430639 | 70430639 | Human | | name |
| 597796378 | CV3694722 | single nucleotide variant | NM_014505.6(KCNMB4):c.307G>A (p.Asp103Asn) | not specified [RCV004935451] | uncertain significance | 12 | 70367041 | 70367041 | Human | | name |
| 597796379 | CV3694724 | single nucleotide variant | NM_014505.6(KCNMB4):c.314A>G (p.His105Arg) | not specified [RCV004935452] | uncertain significance | 12 | 70367048 | 70367048 | Human | | name |