| 8649410 | CV125984 | single nucleotide variant | NM_001040456.1(RHBDD2):c.178+67C>G | Lung cancer [RCV000106471] | uncertain significance | 7 | 75879327 | 75879327 | Human | | name |
| 155902851 | CV2386356 | single nucleotide variant | NM_001040456.3(RHBDD2):c.7G>A (p.Ala3Thr) | not specified [RCV004228691] | uncertain significance | 7 | 75879089 | 75879089 | Human | | name |
| 156204117 | CV2300787 | single nucleotide variant | NM_001040456.3(RHBDD2):c.16C>T (p.Pro6Ser) | not specified [RCV004155715] | uncertain significance | 7 | 75879098 | 75879098 | Human | | name |
| 597788258 | CV3586468 | single nucleotide variant | NM_001040456.3(RHBDD2):c.17C>T (p.Pro6Leu) | not specified [RCV004855450] | uncertain significance | 7 | 75879099 | 75879099 | Human | | name |
| 156134905 | CV2362131 | single nucleotide variant | NM_001040456.3(RHBDD2):c.36C>G (p.Cys12Trp) | not specified [RCV004209935] | uncertain significance | 7 | 75879118 | 75879118 | Human | | name |
| 401894470 | CV2788159 | single nucleotide variant | NM_001040456.3(RHBDD2):c.49G>A (p.Val17Met) | not specified [RCV004352777] | uncertain significance | 7 | 75879131 | 75879131 | Human | | name |
| 405716386 | CV3309320 | single nucleotide variant | NM_001040456.3(RHBDD2):c.64T>A (p.Phe22Ile) | not specified [RCV004449259] | uncertain significance | 7 | 75879146 | 75879146 | Human | | name |
| 8632634 | CV87849 | single nucleotide variant | NM_001040456.1(RHBDD2):c.465C>T (p.Ala155=) | Malignant melanoma [RCV000067941] | not provided | 7 | 75882115 | 75882115 | Human | | name |
| 9691270 | CV172086 | single nucleotide variant | NM_001040456.3(RHBDD2):c.254G>A (p.Arg85His) | not provided [RCV000149778] | uncertain significance|not provided | 7 | 75881904 | 75881904 | Human | | name |
| 156134327 | CV2196019 | single nucleotide variant | NM_001040456.3(RHBDD2):c.253C>T (p.Arg85Cys) | not specified [RCV004072262] | uncertain significance | 7 | 75881903 | 75881903 | Human | | name |
| 401922536 | CV2825807 | single nucleotide variant | NM_001040456.3(RHBDD2):c.1008G>A (p.Val336=) | not provided [RCV003433903] | likely benign | 7 | 75888262 | 75888262 | Human | | name |
| 405716352 | CV3309316 | single nucleotide variant | NM_001040456.3(RHBDD2):c.248T>C (p.Ile83Thr) | not specified [RCV004449255] | uncertain significance | 7 | 75881898 | 75881898 | Human | | name |
| 597776036 | CV3586466 | single nucleotide variant | NM_001040456.3(RHBDD2):c.293G>A (p.Arg98His) | not specified [RCV004852410] | uncertain significance | 7 | 75881943 | 75881943 | Human | | name |
| 597776049 | CV3586472 | single nucleotide variant | NM_001040456.3(RHBDD2):c.292C>T (p.Arg98Cys) | not specified [RCV004852413] | uncertain significance | 7 | 75881942 | 75881942 | Human | | name |
| 598189656 | CV3902649 | single nucleotide variant | NM_001040456.3(RHBDD2):c.139G>A (p.Gly47Ser) | not specified [RCV005266743] | uncertain significance | 7 | 75879221 | 75879221 | Human | | name |
| 598189674 | CV3902651 | single nucleotide variant | NM_001040456.3(RHBDD2):c.170A>G (p.Asn57Ser) | not specified [RCV005266745] | uncertain significance | 7 | 75879252 | 75879252 | Human | | name |
| 156276945 | CV2209837 | single nucleotide variant | NM_001040456.3(RHBDD2):c.654C>G (p.Phe218Leu) | not specified [RCV004076300] | uncertain significance | 7 | 75883765 | 75883765 | Human | | name |
| 156256083 | CV2307774 | single nucleotide variant | NM_001040456.3(RHBDD2):c.632C>T (p.Ala211Val) | not specified [RCV004168460] | uncertain significance | 7 | 75883743 | 75883743 | Human | | name |
| 156339691 | CV2351621 | single nucleotide variant | NM_001040456.3(RHBDD2):c.725C>T (p.Ala242Val) | not specified [RCV004195338] | uncertain significance | 7 | 75883836 | 75883836 | Human | | name |
| 156054711 | CV2388626 | single nucleotide variant | NM_001040456.3(RHBDD2):c.613G>A (p.Asp205Asn) | not specified [RCV004239507] | uncertain significance | 7 | 75883724 | 75883724 | Human | | name |
| 329385741 | CV2462269 | single nucleotide variant | NM_001040456.3(RHBDD2):c.820C>G (p.His274Asp) | not specified [RCV004266264] | uncertain significance | 7 | 75888074 | 75888074 | Human | | name |
| 401746013 | CV2695483 | single nucleotide variant | NM_001040456.3(RHBDD2):c.361T>C (p.Ser121Pro) | not specified [RCV004305669] | uncertain significance | 7 | 75882011 | 75882011 | Human | | name |
| 401780507 | CV2716807 | single nucleotide variant | NM_001040456.3(RHBDD2):c.937A>G (p.Asn313Asp) | not specified [RCV004329627] | uncertain significance | 7 | 75888191 | 75888191 | Human | | name |
| 401873462 | CV2761473 | single nucleotide variant | NM_001040456.3(RHBDD2):c.758C>T (p.Ser253Phe) | not specified [RCV004334646] | uncertain significance | 7 | 75888012 | 75888012 | Human | | name |
| 401881018 | CV2787786 | single nucleotide variant | NM_001040456.3(RHBDD2):c.872T>C (p.Met291Thr) | not specified [RCV004356688] | uncertain significance | 7 | 75888126 | 75888126 | Human | | name |
| 405716364 | CV3309317 | single nucleotide variant | NM_001040456.3(RHBDD2):c.445C>A (p.Arg149Ser) | not specified [RCV004449256] | uncertain significance | 7 | 75882095 | 75882095 | Human | | name |
| 405716371 | CV3309318 | single nucleotide variant | NM_001040456.3(RHBDD2):c.542C>T (p.Thr181Ile) | not specified [RCV004449257] | uncertain significance | 7 | 75882192 | 75882192 | Human | | name |
| 405716380 | CV3309319 | single nucleotide variant | NM_001040456.3(RHBDD2):c.639G>T (p.Lys213Asn) | not specified [RCV004449258] | uncertain significance | 7 | 75883750 | 75883750 | Human | | name |
| 405716402 | CV3309322 | single nucleotide variant | NM_001040456.3(RHBDD2):c.959A>C (p.Tyr320Ser) | not specified [RCV004449261] | uncertain significance | 7 | 75888213 | 75888213 | Human | | name |
| 405716408 | CV3309323 | single nucleotide variant | NM_001040456.3(RHBDD2):c.971C>T (p.Ala324Val) | not specified [RCV004449262] | uncertain significance | 7 | 75888225 | 75888225 | Human | | name |
| 407474453 | CV3472879 | single nucleotide variant | NM_001040456.3(RHBDD2):c.442G>A (p.Val148Ile) | not specified [RCV004663003] | uncertain significance | 7 | 75882092 | 75882092 | Human | | name |
| 407474457 | CV3472880 | single nucleotide variant | NM_001040456.3(RHBDD2):c.583G>A (p.Ala195Thr) | not specified [RCV004663004] | uncertain significance | 7 | 75882233 | 75882233 | Human | | name |
| 407474461 | CV3472881 | single nucleotide variant | NM_001040456.3(RHBDD2):c.521C>T (p.Ala174Val) | not specified [RCV004663005] | uncertain significance | 7 | 75882171 | 75882171 | Human | | name |
| 407474468 | CV3472883 | single nucleotide variant | NM_001040456.3(RHBDD2):c.335T>C (p.Ile112Thr) | not specified [RCV004663007] | uncertain significance | 7 | 75881985 | 75881985 | Human | | name |
| 597788254 | CV3586465 | single nucleotide variant | NM_001040456.3(RHBDD2):c.334A>G (p.Ile112Val) | not specified [RCV004855449] | uncertain significance | 7 | 75881984 | 75881984 | Human | | name |
| 597776040 | CV3586467 | single nucleotide variant | NM_001040456.3(RHBDD2):c.994C>T (p.Pro332Ser) | not specified [RCV004852411] | uncertain significance | 7 | 75888248 | 75888248 | Human | | name |
| 597788262 | CV3586469 | single nucleotide variant | NM_001040456.3(RHBDD2):c.887C>T (p.Pro296Leu) | not specified [RCV004855451] | uncertain significance | 7 | 75888141 | 75888141 | Human | | name |
| 597788263 | CV3586470 | single nucleotide variant | NM_001040456.3(RHBDD2):c.662G>T (p.Ser221Ile) | not specified [RCV004855452] | uncertain significance | 7 | 75883773 | 75883773 | Human | | name |
| 597776045 | CV3586471 | single nucleotide variant | NM_001040456.3(RHBDD2):c.503C>T (p.Pro168Leu) | not specified [RCV004852412] | uncertain significance | 7 | 75882153 | 75882153 | Human | | name |
| 597776053 | CV3586473 | single nucleotide variant | NM_001040456.3(RHBDD2):c.536C>T (p.Pro179Leu) | not specified [RCV004852414] | uncertain significance | 7 | 75882186 | 75882186 | Human | | name |
| 597788273 | CV3586475 | single nucleotide variant | NM_001040456.3(RHBDD2):c.742A>C (p.Asn248His) | not specified [RCV004855454] | uncertain significance | 7 | 75887996 | 75887996 | Human | | name |
| 597788277 | CV3586476 | single nucleotide variant | NM_001040456.3(RHBDD2):c.743A>C (p.Asn248Thr) | not specified [RCV004855455] | uncertain significance | 7 | 75887997 | 75887997 | Human | | name |
| 598189626 | CV3902645 | single nucleotide variant | NM_001040456.3(RHBDD2):c.815C>T (p.Thr272Met) | not specified [RCV005266739] | likely benign | 7 | 75888069 | 75888069 | Human | | name |
| 598189633 | CV3902646 | single nucleotide variant | NM_001040456.3(RHBDD2):c.446G>A (p.Arg149His) | not specified [RCV005266740] | uncertain significance | 7 | 75882096 | 75882096 | Human | | name |
| 598189649 | CV3902648 | single nucleotide variant | NM_001040456.3(RHBDD2):c.560T>C (p.Val187Ala) | not specified [RCV005266742] | uncertain significance | 7 | 75882210 | 75882210 | Human | | name |
| 598189665 | CV3902650 | single nucleotide variant | NM_001040456.3(RHBDD2):c.683T>A (p.Val228Glu) | not specified [RCV005266744] | uncertain significance | 7 | 75883794 | 75883794 | Human | | name |
| 8632633 | CV87848 | single nucleotide variant | NM_001040456.1(RHBDD2):c.464C>T (p.Ala155Val) | Malignant melanoma [RCV000067940] | not provided | 7 | 75882114 | 75882114 | Human | | name |
| 156247330 | CV2202875 | single nucleotide variant | NM_001040456.3(RHBDD2):c.1010A>C (p.Asn337Thr) | not specified [RCV004069151] | uncertain significance | 7 | 75888264 | 75888264 | Human | | name |
