| 15196376 | CV761907 | single nucleotide variant | NM_005955.3(MTF1):c.204A>C (p.Gly68=) | not provided [RCV000934202] | benign | 1 | 37857455 | 37857455 | Human | | name |
| 15106051 | CV761906 | single nucleotide variant | NM_005955.3(MTF1):c.684G>A (p.Thr228=) | not provided [RCV000937711] | likely benign | 1 | 37838720 | 37838720 | Human | | name |
| 155980529 | CV2223037 | single nucleotide variant | NM_005955.3(MTF1):c.250A>G (p.Ile84Val) | not specified [RCV004103618] | uncertain significance | 1 | 37857409 | 37857409 | Human | | name |
| 156168374 | CV2399136 | single nucleotide variant | NM_005955.3(MTF1):c.251T>C (p.Ile84Thr) | not specified [RCV004246569] | uncertain significance | 1 | 37857408 | 37857408 | Human | | name |
| 401887773 | CV2770430 | single nucleotide variant | NM_005955.3(MTF1):c.170C>A (p.Thr57Asn) | not specified [RCV004358072] | uncertain significance | 1 | 37857489 | 37857489 | Human | | name |
| 401872156 | CV2792996 | single nucleotide variant | NM_005955.3(MTF1):c.244C>T (p.His82Tyr) | not specified [RCV004360335] | uncertain significance | 1 | 37857415 | 37857415 | Human | | name |
| 598214946 | CV3989943 | single nucleotide variant | NM_005955.3(MTF1):c.179A>T (p.Asp60Val) | not specified [RCV005378659] | uncertain significance | 1 | 37857480 | 37857480 | Human | | name |
| 15191655 | CV696718 | single nucleotide variant | NM_005955.3(MTF1):c.189C>A (p.Asp63Glu) | not provided [RCV000954839] | benign | 1 | 37857470 | 37857470 | Human | | name |
| 15168928 | CV732427 | single nucleotide variant | NM_005955.3(MTF1):c.1224G>A (p.Pro408=) | not provided [RCV000904956] | likely benign | 1 | 37822664 | 37822664 | Human | | name |
| 15138521 | CV746463 | single nucleotide variant | NM_005955.3(MTF1):c.2163A>G (p.Leu721=) | not provided [RCV000921348] | likely benign | 1 | 37815235 | 37815235 | Human | | name |
| 8629527 | CV84674 | single nucleotide variant | NM_005955.2(MTF1):c.2046T>A (p.Pro682=) | Malignant melanoma [RCV000064756] | not provided | 1 | 37815352 | 37815352 | Human | | name |
| 156127043 | CV2283760 | single nucleotide variant | NM_005955.3(MTF1):c.620G>T (p.Cys207Phe) | not specified [RCV004142281] | uncertain significance | 1 | 37839947 | 37839947 | Human | | name |
| 156196536 | CV2306732 | single nucleotide variant | NM_005955.3(MTF1):c.784G>A (p.Asp262Asn) | not specified [RCV004159317] | uncertain significance | 1 | 37835740 | 37835740 | Human | | name |
| 405664901 | CV3372932 | single nucleotide variant | NM_005955.3(MTF1):c.962A>G (p.Asn321Ser) | not specified [RCV004513946] | likely benign | 1 | 37835107 | 37835107 | Human | | name |
| 597638949 | CV3564447 | single nucleotide variant | NM_005955.3(MTF1):c.305A>G (p.Gln102Arg) | not specified [RCV004825024] | uncertain significance | 1 | 37857354 | 37857354 | Human | | name |
| 156097498 | CV2206820 | single nucleotide variant | NM_005955.3(MTF1):c.2053G>A (p.Gly685Arg) | not specified [RCV004083496] | uncertain significance | 1 | 37815345 | 37815345 | Human | | name |
| 156329680 | CV2216472 | single nucleotide variant | NM_005955.3(MTF1):c.1568A>C (p.Gln523Pro) | not specified [RCV004097281] | uncertain significance | 1 | 37822320 | 37822320 | Human | | name |
| 156264436 | CV2282661 | single nucleotide variant | NM_005955.3(MTF1):c.1251A>C (p.Leu417Phe) | not specified [RCV004135213] | uncertain significance | 1 | 37822637 | 37822637 | Human | | name |
| 156297287 | CV2297663 | single nucleotide variant | NM_005955.3(MTF1):c.1471G>A (p.Ala491Thr) | not specified [RCV004155349] | uncertain significance | 1 | 37822417 | 37822417 | Human | | name |
| 156270645 | CV2312213 | single nucleotide variant | NM_005955.3(MTF1):c.2063C>T (p.Ser688Phe) | not specified [RCV004165108] | uncertain significance | 1 | 37815335 | 37815335 | Human | | name |
| 156035933 | CV2373945 | single nucleotide variant | NM_005955.3(MTF1):c.1972C>G (p.Pro658Ala) | not specified [RCV004227080] | uncertain significance | 1 | 37815426 | 37815426 | Human | | name |
| 156084129 | CV2381960 | single nucleotide variant | NM_005955.3(MTF1):c.1327C>T (p.Pro443Ser) | not specified [RCV004225892] | uncertain significance | 1 | 37822561 | 37822561 | Human | | name |
| 156051465 | CV2386352 | single nucleotide variant | NM_005955.3(MTF1):c.1475C>T (p.Pro492Leu) | not specified [RCV004228687] | uncertain significance | 1 | 37822413 | 37822413 | Human | | name |
| 155968933 | CV2391517 | single nucleotide variant | NM_005955.3(MTF1):c.2096G>A (p.Arg699Gln) | not specified [RCV004239902] | uncertain significance | 1 | 37815302 | 37815302 | Human | | name |
| 156435139 | CV2403398 | single nucleotide variant | NM_005955.3(MTF1):c.1051C>T (p.Arg351Ter) | Autism spectrum disorder [RCV003127334] | uncertain significance | 1 | 37832262 | 37832262 | Human | 2 | name |
| 329356543 | CV2430801 | single nucleotide variant | NM_005955.3(MTF1):c.2204T>C (p.Ile735Thr) | not specified [RCV004253977] | uncertain significance | 1 | 37815194 | 37815194 | Human | | name |
| 401747628 | CV2688965 | single nucleotide variant | NM_005955.3(MTF1):c.1525G>A (p.Ala509Thr) | not specified [RCV004305751] | uncertain significance | 1 | 37822363 | 37822363 | Human | | name |
| 401763952 | CV2725373 | single nucleotide variant | NM_005955.3(MTF1):c.1573A>G (p.Thr525Ala) | not specified [RCV004320020] | uncertain significance | 1 | 37822315 | 37822315 | Human | | name |
| 401862898 | CV2758822 | single nucleotide variant | NM_005955.3(MTF1):c.2222G>T (p.Gly741Val) | not specified [RCV004337871] | uncertain significance | 1 | 37815176 | 37815176 | Human | | name |
| 401885188 | CV2771008 | single nucleotide variant | NM_005955.3(MTF1):c.1288C>A (p.Pro430Thr) | not specified [RCV004344024] | uncertain significance | 1 | 37822600 | 37822600 | Human | | name |
| 405657883 | CV3372858 | single nucleotide variant | NM_005955.3(MTF1):c.1063A>G (p.Ser355Gly) | not specified [RCV004511893] | uncertain significance | 1 | 37832250 | 37832250 | Human | | name |
| 405657889 | CV3372860 | single nucleotide variant | NM_005955.3(MTF1):c.1246T>C (p.Ser416Pro) | not specified [RCV004511895] | uncertain significance | 1 | 37822642 | 37822642 | Human | | name |
| 405657926 | CV3372873 | single nucleotide variant | NM_005955.3(MTF1):c.1460C>T (p.Pro487Leu) | not specified [RCV004511908] | uncertain significance | 1 | 37822428 | 37822428 | Human | | name |
| 405664703 | CV3372891 | single nucleotide variant | NM_005955.3(MTF1):c.1643C>G (p.Pro548Arg) | not specified [RCV004513905] | uncertain significance | 1 | 37822245 | 37822245 | Human | | name |
| 405664737 | CV3372898 | single nucleotide variant | NM_005955.3(MTF1):c.2024C>A (p.Ala675Glu) | not specified [RCV004513912] | uncertain significance | 1 | 37815374 | 37815374 | Human | | name |
| 405664748 | CV3372900 | single nucleotide variant | NM_005955.3(MTF1):c.2033T>C (p.Phe678Ser) | not specified [RCV004513914] | uncertain significance | 1 | 37815365 | 37815365 | Human | | name |
| 407507174 | CV3447418 | single nucleotide variant | NM_005955.3(MTF1):c.1529C>T (p.Ala510Val) | not specified [RCV004646717] | uncertain significance | 1 | 37822359 | 37822359 | Human | | name |
| 407475945 | CV3447419 | single nucleotide variant | NM_005955.3(MTF1):c.1285G>A (p.Glu429Lys) | not specified [RCV004638469] | uncertain significance | 1 | 37822603 | 37822603 | Human | | name |
| 407507176 | CV3447420 | single nucleotide variant | NM_005955.3(MTF1):c.1219G>T (p.Val407Phe) | not specified [RCV004646718] | uncertain significance | 1 | 37822669 | 37822669 | Human | | name |
| 407475950 | CV3447422 | single nucleotide variant | NM_005955.3(MTF1):c.1067C>T (p.Thr356Met) | not specified [RCV004638470] | uncertain significance | 1 | 37832246 | 37832246 | Human | | name |
| 407507182 | CV3447423 | single nucleotide variant | NM_005955.3(MTF1):c.2236G>A (p.Gly746Ser) | not specified [RCV004646720] | uncertain significance | 1 | 37815162 | 37815162 | Human | | name |
| 407507183 | CV3447424 | single nucleotide variant | NM_005955.3(MTF1):c.1370C>T (p.Ala457Val) | not specified [RCV004646721] | uncertain significance | 1 | 37822518 | 37822518 | Human | | name |
| 407507186 | CV3447425 | single nucleotide variant | NM_005955.3(MTF1):c.1315G>C (p.Ala439Pro) | not specified [RCV004646722] | uncertain significance | 1 | 37822573 | 37822573 | Human | | name |
| 597638945 | CV3564444 | single nucleotide variant | NM_005955.3(MTF1):c.1933C>T (p.Arg645Trp) | not specified [RCV004825023] | uncertain significance | 1 | 37815465 | 37815465 | Human | | name |
| 597648877 | CV3564445 | single nucleotide variant | NM_005955.3(MTF1):c.1725A>G (p.Ile575Met) | not specified [RCV004833432] | uncertain significance | 1 | 37822163 | 37822163 | Human | | name |
| 597648886 | CV3564446 | single nucleotide variant | NM_005955.3(MTF1):c.1546G>T (p.Val516Leu) | not specified [RCV004833433] | uncertain significance | 1 | 37822342 | 37822342 | Human | | name |
| 597638956 | CV3564448 | single nucleotide variant | NM_005955.3(MTF1):c.2140G>T (p.Ala714Ser) | not specified [RCV004825025] | uncertain significance | 1 | 37815258 | 37815258 | Human | | name |
| 598180963 | CV3989939 | single nucleotide variant | NM_005955.3(MTF1):c.1222C>G (p.Pro408Ala) | not specified [RCV005372205] | uncertain significance | 1 | 37822666 | 37822666 | Human | | name |
| 598214934 | CV3989940 | single nucleotide variant | NM_005955.3(MTF1):c.1479G>T (p.Gln493His) | not specified [RCV005378657] | uncertain significance | 1 | 37822409 | 37822409 | Human | | name |
| 598180969 | CV3989941 | single nucleotide variant | NM_005955.3(MTF1):c.1934G>A (p.Arg645Gln) | not specified [RCV005372206] | uncertain significance | 1 | 37815464 | 37815464 | Human | | name |
| 598214940 | CV3989942 | single nucleotide variant | NM_005955.3(MTF1):c.2204T>A (p.Ile735Asn) | not specified [RCV005378658] | uncertain significance | 1 | 37815194 | 37815194 | Human | | name |
| 598180974 | CV3989944 | single nucleotide variant | NM_005955.3(MTF1):c.1822A>G (p.Ser608Gly) | not specified [RCV005372207] | uncertain significance | 1 | 37817428 | 37817428 | Human | | name |
| 15163966 | CV696717 | single nucleotide variant | NM_005955.3(MTF1):c.1318C>T (p.Pro440Ser) | not provided [RCV000948221] | benign | 1 | 37822570 | 37822570 | Human | | name |
| 15104510 | CV718954 | single nucleotide variant | NM_005955.3(MTF1):c.1333C>T (p.Pro445Ser) | not provided [RCV000892899] | likely benign | 1 | 37822555 | 37822555 | Human | | name |
| 15189899 | CV718955 | single nucleotide variant | NM_005955.3(MTF1):c.1091C>T (p.Thr364Ile) | not provided [RCV000887952] | likely benign | 1 | 37823790 | 37823790 | Human | | name |
