ClinVar Miner

List of variants in gene combination MTHFD1, ZBTB25 studied for not provided

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Total variants: 81
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HGVS dbSNP gnomAD frequency
NM_005956.4(MTHFD1):c.2305C>T (p.Leu769Phe) rs17857382 0.03087
NM_005956.4(MTHFD1):c.2282C>T (p.Thr761Met) rs10813 0.02775
NM_005956.4(MTHFD1):c.2315G>A (p.Arg772His) rs149899012 0.00691
NM_005956.4(MTHFD1):c.2566-4C>T rs143887854 0.00237
NM_005956.4(MTHFD1):c.2408A>G (p.Gln803Arg) rs149791016 0.00057
NM_005956.4(MTHFD1):c.2628G>A (p.Glu876=) rs145762961 0.00047
NM_005956.4(MTHFD1):c.2458-7G>A rs200935483 0.00029
NM_005956.4(MTHFD1):c.2280-16A>G rs773893134 0.00020
NM_005956.4(MTHFD1):c.2412A>G (p.Arg804=) rs368053637 0.00013
NM_005956.4(MTHFD1):c.2565+17T>C rs200582437 0.00006
NM_005956.4(MTHFD1):c.2283G>A (p.Thr761=) rs777230520 0.00005
NM_005956.4(MTHFD1):c.2530G>A (p.Glu844Lys) rs777892594 0.00005
NM_005956.4(MTHFD1):c.2682C>T (p.Ser894=) rs565206627 0.00005
NM_005956.4(MTHFD1):c.2718+18G>A rs200629267 0.00005
NM_005956.4(MTHFD1):c.2558C>T (p.Thr853Met) rs201204855 0.00004
NM_005956.4(MTHFD1):c.2307C>T (p.Leu769=) rs773683051 0.00003
NM_005956.4(MTHFD1):c.2314C>T (p.Arg772Cys) rs372827157 0.00003
NM_005956.4(MTHFD1):c.2349G>C (p.Val783=) rs61985661 0.00003
NM_005956.4(MTHFD1):c.2619C>T (p.His873=) rs914153061 0.00003
NM_005956.4(MTHFD1):c.2665C>T (p.Arg889Cys) rs767011731 0.00003
NM_005956.4(MTHFD1):c.2666G>A (p.Arg889His) rs760130182 0.00003
NM_005956.4(MTHFD1):c.2667C>T (p.Arg889=) rs763646367 0.00003
NM_005956.4(MTHFD1):c.2675G>A (p.Arg892His) rs758973638 0.00003
NM_005956.4(MTHFD1):c.2679C>G (p.Ala893=) rs371245049 0.00003
NM_005956.4(MTHFD1):c.2280-20A>G rs748890709 0.00002
NM_005956.4(MTHFD1):c.2404G>A (p.Val802Ile) rs771687911 0.00002
NM_005956.4(MTHFD1):c.2584A>G (p.Ile862Val) rs746400551 0.00002
NM_005956.4(MTHFD1):c.2668G>A (p.Asp890Asn) rs750902671 0.00002
NM_005956.4(MTHFD1):c.2676C>T (p.Arg892=) rs780386825 0.00002
NM_005956.4(MTHFD1):c.2718+19G>T rs903176404 0.00002
NM_005956.4(MTHFD1):c.2288C>T (p.Thr763Ile) rs369285610 0.00001
NM_005956.4(MTHFD1):c.2299C>G (p.Leu767Val) rs2550506858 0.00001
NM_005956.4(MTHFD1):c.2463A>T (p.Pro821=) rs1034316320 0.00001
NM_005956.4(MTHFD1):c.2482A>G (p.Ile828Val) rs758271489 0.00001
NM_005956.4(MTHFD1):c.2529C>T (p.Pro843=) rs1369613607 0.00001
NM_005956.4(MTHFD1):c.2555del (p.Tyr852fs) rs1326829113 0.00001
NM_005956.4(MTHFD1):c.2590A>G (p.Met864Val) rs1368736054 0.00001
NM_005956.4(MTHFD1):c.2648G>A (p.Gly883Asp) rs1287071530 0.00001
NM_005956.4(MTHFD1):c.2655T>C (p.Ile885=) rs1177823217 0.00001
NM_005956.4(MTHFD1):c.2661C>T (p.Pro887=) rs759391345 0.00001
NM_005956.4(MTHFD1):c.2674C>T (p.Arg892Cys) rs1038153439 0.00001
NM_005956.4(MTHFD1):c.2684T>C (p.Val895Ala) rs991768162 0.00001
NM_005956.4(MTHFD1):c.2717C>T (p.Thr906Met) rs371285981 0.00001
NM_005956.4(MTHFD1):c.2718+17A>G rs560869064 0.00001
NM_005956.4(MTHFD1):c.2719-17G>A rs374229822 0.00001
NM_005956.4(MTHFD1):c.2747G>A (p.Arg916Gln) rs563992464 0.00001
NM_005956.4(MTHFD1):c.2280-19T>C
NM_005956.4(MTHFD1):c.2280-4A>C rs2550506840
NM_005956.4(MTHFD1):c.2280-8C>A rs2550506835
NM_005956.4(MTHFD1):c.2303A>T (p.Asp768Val)
NM_005956.4(MTHFD1):c.2311A>G (p.Ser771Gly) rs763240378
NM_005956.4(MTHFD1):c.2312G>C (p.Ser771Thr) rs766552980
NM_005956.4(MTHFD1):c.2318T>A (p.Leu773His) rs2550506880
NM_005956.4(MTHFD1):c.2347G>A (p.Val783Met) rs1029133044
NM_005956.4(MTHFD1):c.2353T>C (p.Cys785Arg) rs2140982417
NM_005956.4(MTHFD1):c.2392C>A (p.Leu798Met) rs200744141
NM_005956.4(MTHFD1):c.2400G>A (p.Gln800=) rs2550506930
NM_005956.4(MTHFD1):c.2403C>G (p.Ala801=)
NM_005956.4(MTHFD1):c.2427C>T (p.Pro809=) rs2140982488
NM_005956.4(MTHFD1):c.2457+4G>C rs2078338046
NM_005956.4(MTHFD1):c.2460C>T (p.Leu820=)
NM_005956.4(MTHFD1):c.2479_2480insTTGCACA (p.Arg827fs)
NM_005956.4(MTHFD1):c.2535T>G (p.Ala845=) rs775641356
NM_005956.4(MTHFD1):c.2548G>T (p.Glu850Ter) rs2140987898
NM_005956.4(MTHFD1):c.2565+13T>G rs2140987935
NM_005956.4(MTHFD1):c.2566-15C>G
NM_005956.4(MTHFD1):c.2576A>G (p.Asn859Ser) rs2140988995
NM_005956.4(MTHFD1):c.2595T>C (p.Ala865=) rs780440085
NM_005956.4(MTHFD1):c.2605T>C (p.Leu869=)
NM_005956.4(MTHFD1):c.2640C>G (p.Val880=) rs2078438814
NM_005956.4(MTHFD1):c.2718+20G>T rs1430285060
NM_005956.4(MTHFD1):c.2718+9A>C rs2078441021
NM_005956.4(MTHFD1):c.2718G>A (p.Thr906=) rs2550508505
NM_005956.4(MTHFD1):c.2719-6T>A rs2078506200
NM_005956.4(MTHFD1):c.2721G>A (p.Met907Ile)
NM_005956.4(MTHFD1):c.2739C>G (p.Leu913=) rs1354264402
NM_005956.4(MTHFD1):c.2751C>G (p.Pro917=)
NM_005956.4(MTHFD1):c.2755T>A (p.Phe919Ile) rs2140993701
NM_005956.4(MTHFD1):c.2766T>C (p.Ile922=)
NM_005956.4(MTHFD1):c.2787A>G (p.Glu929=)
NM_005956.4(MTHFD1):c.2801T>C (p.Leu934Ser) rs2140993732

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