| 15152765 | CV731012 | single nucleotide variant | NM_032857.5(LACTB):c.616-7C>A | not provided [RCV000879873] | benign | 15 | 63127346 | 63127346 | Human | | name |
| 405808636 | CV3287003 | single nucleotide variant | NM_032857.5(LACTB):c.7C>T (p.Arg3Trp) | not specified [RCV004407153] | uncertain significance | 15 | 63121878 | 63121878 | Human | | name |
| 10411845 | CV205478 | single nucleotide variant | NM_032857.5(LACTB):c.46G>C (p.Gly16Arg) | Abnormality of neuronal migration [RCV000201410] | pathogenic|benign | 15 | 63121917 | 63121917 | Human | 1 | name |
| 156199611 | CV2237575 | single nucleotide variant | NM_032857.5(LACTB):c.50G>C (p.Gly17Ala) | not specified [RCV004106513] | uncertain significance | 15 | 63121921 | 63121921 | Human | | name |
| 597630980 | CV3692760 | single nucleotide variant | NM_032857.5(LACTB):c.43C>A (p.Pro15Thr) | not specified [RCV004939594] | uncertain significance | 15 | 63121914 | 63121914 | Human | | name |
| 15200328 | CV703281 | single nucleotide variant | NM_032857.5(LACTB):c.46G>A (p.Gly16Arg) | not provided [RCV000957298] | benign | 15 | 63121917 | 63121917 | Human | | name |
| 15200332 | CV703282 | single nucleotide variant | NM_032857.5(LACTB):c.73C>T (p.Arg25Cys) | not provided [RCV000957299] | benign | 15 | 63121944 | 63121944 | Human | | name |
| 156076186 | CV2291486 | single nucleotide variant | NM_032857.5(LACTB):c.185G>T (p.Gly62Val) | not specified [RCV004155802] | uncertain significance | 15 | 63122056 | 63122056 | Human | | name |
| 401750655 | CV2715718 | single nucleotide variant | NM_032857.5(LACTB):c.269C>G (p.Pro90Arg) | not specified [RCV004328863] | uncertain significance | 15 | 63122140 | 63122140 | Human | | name |
| 405808624 | CV3286997 | single nucleotide variant | NM_032857.5(LACTB):c.184G>C (p.Gly62Arg) | not specified [RCV004407147] | uncertain significance | 15 | 63122055 | 63122055 | Human | | name |
| 405808626 | CV3286998 | single nucleotide variant | NM_032857.5(LACTB):c.206C>T (p.Pro69Leu) | not specified [RCV004407148] | uncertain significance | 15 | 63122077 | 63122077 | Human | | name |
| 405808628 | CV3286999 | single nucleotide variant | NM_032857.5(LACTB):c.277C>A (p.Pro93Thr) | not specified [RCV004407149] | uncertain significance | 15 | 63122148 | 63122148 | Human | | name |
| 407460729 | CV3456019 | single nucleotide variant | NM_032857.5(LACTB):c.151G>T (p.Ala51Ser) | not specified [RCV004633805] | uncertain significance | 15 | 63122022 | 63122022 | Human | | name |
| 597625082 | CV3692755 | single nucleotide variant | NM_032857.5(LACTB):c.203C>G (p.Ser68Cys) | not specified [RCV004938103] | uncertain significance | 15 | 63122074 | 63122074 | Human | | name |
| 597630976 | CV3692757 | single nucleotide variant | NM_032857.5(LACTB):c.229T>A (p.Ser77Thr) | not specified [RCV004939593] | uncertain significance | 15 | 63122100 | 63122100 | Human | | name |
| 15157819 | CV726174 | single nucleotide variant | NM_032857.5(LACTB):c.1440G>A (p.Arg480=) | not provided [RCV000880890] | benign | 15 | 63141601 | 63141601 | Human | | name |
| 155919518 | CV2254885 | single nucleotide variant | NM_032857.5(LACTB):c.529T>G (p.Leu177Val) | not specified [RCV004117131] | uncertain significance | 15 | 63126963 | 63126963 | Human | | name |
| 155999282 | CV2261073 | single nucleotide variant | NM_032857.5(LACTB):c.471G>C (p.Glu157Asp) | not specified [RCV004127721] | uncertain significance | 15 | 63126905 | 63126905 | Human | | name |
| 155902591 | CV2274714 | single nucleotide variant | NM_032857.5(LACTB):c.921A>T (p.Leu307Phe) | not specified [RCV004139082] | uncertain significance | 15 | 63127658 | 63127658 | Human | | name |
| 155959450 | CV2285277 | single nucleotide variant | NM_032857.5(LACTB):c.827G>A (p.Arg276Gln) | not specified [RCV004137373] | uncertain significance | 15 | 63127564 | 63127564 | Human | | name |
| 156067854 | CV2320313 | single nucleotide variant | NM_032857.5(LACTB):c.440A>T (p.Asp147Val) | not specified [RCV004178475] | uncertain significance | 15 | 63126874 | 63126874 | Human | | name |
| 329352301 | CV2452325 | single nucleotide variant | NM_032857.5(LACTB):c.569A>C (p.Gln190Pro) | not specified [RCV004272658] | uncertain significance | 15 | 63127003 | 63127003 | Human | | name |
| 401746033 | CV2678755 | single nucleotide variant | NM_032857.5(LACTB):c.682A>G (p.Lys228Glu) | not specified [RCV004292748] | uncertain significance | 15 | 63127419 | 63127419 | Human | | name |
| 401744472 | CV2697007 | single nucleotide variant | NM_032857.5(LACTB):c.324C>G (p.Ile108Met) | not specified [RCV004292998] | uncertain significance | 15 | 63122195 | 63122195 | Human | | name |
| 405808630 | CV3287000 | single nucleotide variant | NM_032857.5(LACTB):c.376G>A (p.Gly126Ser) | not specified [RCV004407150] | uncertain significance | 15 | 63122654 | 63122654 | Human | | name |
| 405808634 | CV3287002 | single nucleotide variant | NM_032857.5(LACTB):c.520C>T (p.Leu174Phe) | not specified [RCV004407152] | uncertain significance | 15 | 63126954 | 63126954 | Human | | name |
| 405808638 | CV3287004 | single nucleotide variant | NM_032857.5(LACTB):c.806A>C (p.Gln269Pro) | not specified [RCV004407154] | uncertain significance | 15 | 63127543 | 63127543 | Human | | name |
| 405808640 | CV3287005 | single nucleotide variant | NM_032857.5(LACTB):c.904A>G (p.Ile302Val) | not specified [RCV004407155] | uncertain significance | 15 | 63127641 | 63127641 | Human | | name |
| 405808642 | CV3287006 | single nucleotide variant | NM_032857.5(LACTB):c.904A>T (p.Ile302Phe) | not specified [RCV004407156] | uncertain significance | 15 | 63127641 | 63127641 | Human | | name |
| 407480930 | CV3456020 | single nucleotide variant | NM_032857.5(LACTB):c.810G>C (p.Glu270Asp) | not specified [RCV004639826] | likely benign | 15 | 63127547 | 63127547 | Human | | name |
| 407460724 | CV3456021 | single nucleotide variant | NM_032857.5(LACTB):c.947A>G (p.Lys316Arg) | not specified [RCV004633806] | uncertain significance | 15 | 63127684 | 63127684 | Human | | name |
| 597795225 | CV3692758 | single nucleotide variant | NM_032857.5(LACTB):c.599A>T (p.Glu200Val) | not specified [RCV004934799] | uncertain significance | 15 | 63127033 | 63127033 | Human | | name |
| 597630990 | CV3692763 | single nucleotide variant | NM_032857.5(LACTB):c.373C>G (p.Pro125Ala) | not specified [RCV004939597] | uncertain significance | 15 | 63122651 | 63122651 | Human | | name |
| 598222525 | CV3991483 | single nucleotide variant | NM_032857.5(LACTB):c.347A>T (p.His116Leu) | not specified [RCV005361001] | uncertain significance | 15 | 63122218 | 63122218 | Human | | name |
| 598173679 | CV3991484 | single nucleotide variant | NM_032857.5(LACTB):c.826C>T (p.Arg276Trp) | not specified [RCV005370969] | uncertain significance | 15 | 63127563 | 63127563 | Human | | name |
| 598222533 | CV3991485 | single nucleotide variant | NM_032857.5(LACTB):c.628A>T (p.Thr210Ser) | not specified [RCV005361002] | uncertain significance | 15 | 63127365 | 63127365 | Human | | name |
| 156369345 | CV2193953 | single nucleotide variant | NM_032857.5(LACTB):c.1534G>A (p.Val512Ile) | not specified [RCV004074681] | uncertain significance | 15 | 63141695 | 63141695 | Human | | name |
| 155934577 | CV2225337 | single nucleotide variant | NM_032857.5(LACTB):c.1238C>T (p.Ala413Val) | not specified [RCV004100760] | uncertain significance | 15 | 63141399 | 63141399 | Human | | name |
| 156092252 | CV2256656 | single nucleotide variant | NM_032857.5(LACTB):c.1438C>T (p.Arg480Trp) | not specified [RCV004118838] | uncertain significance | 15 | 63141599 | 63141599 | Human | | name |
| 329401952 | CV2458014 | single nucleotide variant | NM_032857.5(LACTB):c.1522A>G (p.Ile508Val) | not specified [RCV004271584] | uncertain significance | 15 | 63141683 | 63141683 | Human | | name |
| 401742116 | CV2677514 | single nucleotide variant | NM_032857.5(LACTB):c.1343C>T (p.Pro448Leu) | not specified [RCV004291622] | uncertain significance | 15 | 63141504 | 63141504 | Human | | name |
| 405808610 | CV3286990 | single nucleotide variant | NM_032857.5(LACTB):c.1012G>A (p.Ala338Thr) | not specified [RCV004407140] | uncertain significance | 15 | 63129544 | 63129544 | Human | | name |
| 405808612 | CV3286991 | single nucleotide variant | NM_032857.5(LACTB):c.1055A>T (p.His352Leu) | not specified [RCV004407141] | uncertain significance | 15 | 63129587 | 63129587 | Human | | name |
| 405808614 | CV3286992 | single nucleotide variant | NM_032857.5(LACTB):c.1145G>A (p.Arg382His) | not specified [RCV004407142] | uncertain significance | 15 | 63141306 | 63141306 | Human | | name |
| 405808616 | CV3286993 | single nucleotide variant | NM_032857.5(LACTB):c.1259T>C (p.Val420Ala) | not specified [RCV004407143] | uncertain significance | 15 | 63141420 | 63141420 | Human | | name |
| 405808618 | CV3286994 | single nucleotide variant | NM_032857.5(LACTB):c.1415C>T (p.Thr472Met) | not specified [RCV004407144] | uncertain significance | 15 | 63141576 | 63141576 | Human | | name |
| 405808620 | CV3286995 | single nucleotide variant | NM_032857.5(LACTB):c.1427G>A (p.Cys476Tyr) | not specified [RCV004407145] | uncertain significance | 15 | 63141588 | 63141588 | Human | | name |
| 405808622 | CV3286996 | single nucleotide variant | NM_032857.5(LACTB):c.1511A>G (p.Asp504Gly) | not specified [RCV004407146] | uncertain significance | 15 | 63141672 | 63141672 | Human | | name |
| 597630972 | CV3692756 | single nucleotide variant | NM_032857.5(LACTB):c.1510G>A (p.Asp504Asn) | not specified [RCV004939592] | uncertain significance | 15 | 63141671 | 63141671 | Human | | name |
| 597795230 | CV3692759 | single nucleotide variant | NM_032857.5(LACTB):c.1364A>G (p.Asp455Gly) | not specified [RCV004934800] | uncertain significance | 15 | 63141525 | 63141525 | Human | | name |
| 597630987 | CV3692762 | single nucleotide variant | NM_032857.5(LACTB):c.1471G>C (p.Gly491Arg) | not specified [RCV004939596] | uncertain significance | 15 | 63141632 | 63141632 | Human | | name |
| 598222542 | CV3991486 | single nucleotide variant | NM_032857.5(LACTB):c.1534G>T (p.Val512Phe) | not specified [RCV005361003] | uncertain significance | 15 | 63141695 | 63141695 | Human | | name |
| 8575720 | CV110071 | single nucleotide variant | NM_001289974.1(LACTBL1):c.416+433C>A | Lung cancer [RCV000090594] | uncertain significance | 1 | 22959509 | 22959509 | Human | | name |
| 405808646 | CV3287008 | single nucleotide variant | NM_016027.3(LACTB2):c.13C>G (p.Leu5Val) | not specified [RCV004407158] | uncertain significance | 8 | 70669108 | 70669108 | Human | | name |
| 408367858 | CV3517944 | single nucleotide variant | NM_016027.3(LACTB2):c.610C>A (p.His204Asn) | LACTB2-related condition [RCV004759277] | uncertain significance | 8 | 70641033 | 70641033 | Human | | name , trait |
| 597630997 | CV3692766 | single nucleotide variant | NM_016027.3(LACTB2):c.17A>C (p.Gln6Pro) | not specified [RCV004939599] | uncertain significance | 8 | 70669104 | 70669104 | Human | | name |
| 597631004 | CV3692768 | single nucleotide variant | NM_016027.3(LACTB2):c.20G>A (p.Arg7His) | not specified [RCV004939601] | uncertain significance | 8 | 70669101 | 70669101 | Human | | name |
| 407480936 | CV3456022 | single nucleotide variant | NM_016027.3(LACTB2):c.28C>G (p.Arg10Gly) | not specified [RCV004639827] | uncertain significance | 8 | 70669093 | 70669093 | Human | | name |
| 156199243 | CV2312977 | single nucleotide variant | NM_016027.3(LACTB2):c.170G>T (p.Ser57Ile) | not specified [RCV004159482] | uncertain significance | 8 | 70661850 | 70661850 | Human | | name |
| 156065184 | CV2346470 | single nucleotide variant | NM_016027.3(LACTB2):c.296A>G (p.Tyr99Cys) | not specified [RCV004206395] | uncertain significance | 8 | 70657873 | 70657873 | Human | | name |
| 405808644 | CV3287007 | single nucleotide variant | NM_016027.3(LACTB2):c.107T>G (p.Val36Gly) | not specified [RCV004407157] | uncertain significance | 8 | 70669014 | 70669014 | Human | | name |
| 405808648 | CV3287009 | single nucleotide variant | NM_016027.3(LACTB2):c.210C>G (p.Ile70Met) | not specified [RCV004407159] | uncertain significance | 8 | 70661810 | 70661810 | Human | | name |
| 597795233 | CV3692764 | single nucleotide variant | NM_016027.3(LACTB2):c.257T>C (p.Ile86Thr) | not specified [RCV004934801] | uncertain significance | 8 | 70661763 | 70661763 | Human | | name |
| 597630993 | CV3692765 | single nucleotide variant | NM_016027.3(LACTB2):c.157C>G (p.Pro53Ala) | not specified [RCV004939598] | uncertain significance | 8 | 70661863 | 70661863 | Human | | name |
| 155961029 | CV2204422 | single nucleotide variant | NM_016027.3(LACTB2):c.340A>G (p.Ile114Val) | not specified [RCV004079230] | uncertain significance | 8 | 70657829 | 70657829 | Human | | name |
| 156096820 | CV2206682 | single nucleotide variant | NM_016027.3(LACTB2):c.656T>C (p.Ile219Thr) | not specified [RCV004083376] | uncertain significance | 8 | 70640987 | 70640987 | Human | | name |
| 155983467 | CV2371286 | single nucleotide variant | NM_016027.3(LACTB2):c.430G>A (p.Gly144Ser) | not specified [RCV004222889] | uncertain significance | 8 | 70644227 | 70644227 | Human | | name |
| 155990183 | CV2374660 | single nucleotide variant | NM_016027.3(LACTB2):c.571A>C (p.Lys191Gln) | not specified [RCV004225277] | uncertain significance | 8 | 70644086 | 70644086 | Human | | name |
| 156346854 | CV2375326 | single nucleotide variant | NM_016027.3(LACTB2):c.659G>A (p.Arg220Gln) | not specified [RCV004232729] | uncertain significance | 8 | 70640984 | 70640984 | Human | | name |
| 405808650 | CV3287010 | single nucleotide variant | NM_016027.3(LACTB2):c.635A>T (p.Gln212Leu) | not specified [RCV004407160] | uncertain significance | 8 | 70641008 | 70641008 | Human | | name |
| 405808654 | CV3287012 | single nucleotide variant | NM_016027.3(LACTB2):c.686G>A (p.Arg229His) | not specified [RCV004407162] | likely benign | 8 | 70640957 | 70640957 | Human | | name |
| 405808656 | CV3287013 | single nucleotide variant | NM_016027.3(LACTB2):c.859C>T (p.His287Tyr) | not specified [RCV004407163] | uncertain significance | 8 | 70637868 | 70637868 | Human | | name |
| 407480943 | CV3456023 | single nucleotide variant | NM_016027.3(LACTB2):c.760C>T (p.His254Tyr) | not specified [RCV004639828] | uncertain significance | 8 | 70638611 | 70638611 | Human | | name |
| 407460720 | CV3456024 | single nucleotide variant | NM_016027.3(LACTB2):c.686G>C (p.Arg229Pro) | not specified [RCV004633807] | uncertain significance | 8 | 70640957 | 70640957 | Human | | name |
| 597630999 | CV3692767 | single nucleotide variant | NM_016027.3(LACTB2):c.585A>G (p.Ile195Met) | not specified [RCV004939600] | uncertain significance | 8 | 70644072 | 70644072 | Human | | name |
| 598196908 | CV3991487 | single nucleotide variant | NM_016027.3(LACTB2):c.718G>C (p.Glu240Gln) | not specified [RCV005355258] | uncertain significance | 8 | 70640925 | 70640925 | Human | | name |
| 401935526 | CV2812457 | single nucleotide variant | NM_001289974.2(LACTBL1):c.1128C>T (p.Asn376=) | not provided [RCV003412895] | likely benign | 1 | 22953655 | 22953655 | Human | | name |
