Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.135800657T>A | CA348592605 | LCT | c.4816A>T (p.Arg1606Ter) c.2960-2519A>T (n.2960-2519A>T) | |
2 | g.135800657T>C | CA348592608 | LCT | c.4816A>G (p.Arg1606Gly) c.2960-2519A>G (n.2960-2519A>G) | |
2 | g.135800657T>G | CA429086354 | LCT | c.4816A>C (p.Arg1606=) c.2960-2519A>C (n.2960-2519A>C) | |
2 | g.135800658G>A | CA429086356 | LCT | c.4815C>T (p.Pro1605=) c.2960-2520C>T (n.2960-2520C>T) | dbSNP |
2 | g.135800658G>C | CA429086358 | LCT | c.4815C>G (p.Pro1605=) c.2960-2520C>G (n.2960-2520C>G) | |
2 | g.135800658G= | CA1290827608 | LCT | c.4815C= (p.Pro1605=) c.2960-2520C= (n.2960-2520C=) | |
2 | g.135800658G>T | CA429086359 | LCT | c.4815C>A (p.Pro1605=) c.2960-2520C>A (n.2960-2520C>A) | |
2 | g.135800659G>A | CA348592612 | LCT | c.4814C>T (p.Pro1605Leu) c.2960-2521C>T (n.2960-2521C>T) | gnomAD v4 |
2 | g.135800659G>C | CA348592619 | LCT | c.4814C>G (p.Pro1605Arg) c.2960-2521C>G (n.2960-2521C>G) | |
2 | g.135800659G>T | CA348592622 | LCT | c.4814C>A (p.Pro1605His) c.2960-2521C>A (n.2960-2521C>A) | |
2 | g.135800660G>A | CA348592624 | LCT | c.4813C>T (p.Pro1605Ser) c.2960-2522C>T (n.2960-2522C>T) | dbSNP |
2 | g.135800660G>C | CA348592631 | LCT | c.4813C>G (p.Pro1605Ala) c.2960-2522C>G (n.2960-2522C>G) | |
2 | g.135800660G= | CA1290827609 | LCT | c.4813C= (p.Pro1605=) c.2960-2522C= (n.2960-2522C=) | |
2 | g.135800660G>T | CA348592628 | LCT | c.4813C>A (p.Pro1605Thr) c.2960-2522C>A (n.2960-2522C>A) | |
2 | g.135800661T>A | CA348592633 | LCT | c.4812A>T (p.Glu1604Asp) c.2960-2523A>T (n.2960-2523A>T) | COSMIC |
2 | g.135800661T>C | CA429086361 | LCT | c.4812A>G (p.Glu1604=) c.2960-2523A>G (n.2960-2523A>G) | dbSNP |
2 | g.135800661T>G | CA348592635 | LCT | c.4812A>C (p.Glu1604Asp) c.2960-2523A>C (n.2960-2523A>C) | |
2 | g.135800661T= | CA1290827610 | LCT | c.4812A= (p.Glu1604=) c.2960-2523A= (n.2960-2523A=) | |
2 | g.135800662T>A | CA348592640 | LCT | c.4811A>T (p.Glu1604Val) c.2960-2524A>T (n.2960-2524A>T) | |
2 | g.135800662T>C | CA348592646 | LCT | c.4811A>G (p.Glu1604Gly) c.2960-2524A>G (n.2960-2524A>G) | |
2 | g.135800662T>G | CA348592644 | LCT | c.4811A>C (p.Glu1604Ala) c.2960-2524A>C (n.2960-2524A>C) | |
2 | g.135800663C>A | CA348592649 | LCT | c.4810G>T (p.Glu1604Ter) c.2960-2525G>T (n.2960-2525G>T) | |
2 | g.135800663C>G | CA348592653 | LCT | c.4810G>C (p.Glu1604Gln) c.2960-2525G>C (n.2960-2525G>C) | |
2 | g.135800663C>T | CA348592655 | LCT | c.4810G>A (p.Glu1604Lys) c.2960-2525G>A (n.2960-2525G>A) | gnomAD v4 |
2 | g.135800664A>C | CA429086368 | LCT | c.4809T>G (p.Ala1603=) c.2960-2526T>G (n.2960-2526T>G) | |
2 | g.135800664A>G | CA429086364 | LCT | c.4809T>C (p.Ala1603=) c.2960-2526T>C (n.2960-2526T>C) | ClinVar |
2 | g.135800664A>T | CA429086366 | LCT | c.4809T>A (p.Ala1603=) c.2960-2526T>A (n.2960-2526T>A) | |
2 | g.135800665G>A | CA348592659 | LCT | c.4808C>T (p.Ala1603Val) c.2960-2527C>T (n.2960-2527C>T) | |
2 | g.135800665G>C | CA348592663 | LCT | c.4808C>G (p.Ala1603Gly) c.2960-2527C>G (n.2960-2527C>G) | COSMIC |
2 | g.135800665G>T | CA348592666 | LCT | c.4808C>A (p.Ala1603Asp) c.2960-2527C>A (n.2960-2527C>A) | |
2 | g.135800666C>A | CA348592670 | LCT | c.4807G>T (p.Ala1603Ser) c.2960-2528G>T (n.2960-2528G>T) | |
2 | g.135800666C>G | CA348592673 | LCT | c.4807G>C (p.Ala1603Pro) c.2960-2528G>C (n.2960-2528G>C) | |
2 | g.135800666C>T | CA348592675 | LCT | c.4807G>A (p.Ala1603Thr) c.2960-2528G>A (n.2960-2528G>A) | |
2 | g.135800667C>A | CA348592683 | LCT | c.4806G>T (p.Trp1602Cys) c.2960-2529G>T (n.2960-2529G>T) | |
2 | g.135800667C>G | CA348592680 | LCT | c.4806G>C (p.Trp1602Cys) c.2960-2529G>C (n.2960-2529G>C) | |
2 | g.135800667C>T | CA348592678 | LCT | c.4806G>A (p.Trp1602Ter) c.2960-2529G>A (n.2960-2529G>A) | |
2 | g.135800668C>A | CA348592688 | LCT | c.4805G>T (p.Trp1602Leu) c.2960-2530G>T (n.2960-2530G>T) | COSMIC |
2 | g.135800668C>G | CA348592690 | LCT | c.4805G>C (p.Trp1602Ser) c.2960-2530G>C (n.2960-2530G>C) | |
2 | g.135800668C>T | CA348592691 | LCT | c.4805G>A (p.Trp1602Ter) c.2960-2530G>A (n.2960-2530G>A) | |
2 | g.135800669A>C | CA348592694 | LCT | c.4804T>G (p.Trp1602Gly) c.2960-2531T>G (n.2960-2531T>G) | |
2 | g.135800669A>G | CA348592697 | LCT | c.4804T>C (p.Trp1602Arg) c.2960-2531T>C (n.2960-2531T>C) | |
2 | g.135800669A>T | CA348592700 | LCT | c.4804T>A (p.Trp1602Arg) c.2960-2531T>A (n.2960-2531T>A) | |
2 | g.135800670G>A | CA429086374 | LCT | c.4803C>T (p.Asp1601=) c.2960-2532C>T (n.2960-2532C>T) | |
2 | g.135800670G>C | CA348592703 | LCT | c.4803C>G (p.Asp1601Glu) c.2960-2532C>G (n.2960-2532C>G) | |
2 | g.135800670G>T | CA348592705 | LCT | c.4803C>A (p.Asp1601Glu) c.2960-2532C>A (n.2960-2532C>A) | |
2 | g.135800671T>A | CA348592708 | LCT | c.4802A>T (p.Asp1601Val) c.2960-2533A>T (n.2960-2533A>T) | |
2 | g.135800671T>C | CA348592711 | LCT | c.4802A>G (p.Asp1601Gly) c.2960-2533A>G (n.2960-2533A>G) | |
2 | g.135800671T>G | CA348592713 | LCT | c.4802A>C (p.Asp1601Ala) c.2960-2533A>C (n.2960-2533A>C) | |
2 | g.135800672C>A | CA348592719 | LCT | c.4801G>T (p.Asp1601Tyr) c.2960-2534G>T (n.2960-2534G>T) | gnomAD v4 |
2 | g.135800672C>G | CA348592722 | LCT | c.4801G>C (p.Asp1601His) c.2960-2534G>C (n.2960-2534G>C) | |
2 | g.135800672C>T | CA348592716 | LCT | c.4801G>A (p.Asp1601Asn) c.2960-2534G>A (n.2960-2534G>A) | |
2 | g.135800673A= | CA1290827611 | LCT | c.4800T= (p.Ser1600=) c.2960-2535T= (n.2960-2535T=) | |
2 | g.135800673A>C | CA348592724 | LCT | c.4800T>G (p.Ser1600Arg) c.2960-2535T>G (n.2960-2535T>G) | |
2 | g.135800673A>G | CA1887771 | LCT | c.4800T>C (p.Ser1600=) c.2960-2535T>C (n.2960-2535T>C) | dbSNP ExAC gnomAD v2 |
2 | g.135800673A>T | CA348592729 | LCT | c.4800T>A (p.Ser1600Arg) c.2960-2535T>A (n.2960-2535T>A) | |
2 | g.135800674C>A | CA348592734 | LCT | c.4799G>T (p.Ser1600Ile) c.2960-2536G>T (n.2960-2536G>T) | |
2 | g.135800674C>G | CA348592736 | LCT | c.4799G>C (p.Ser1600Thr) c.2960-2536G>C (n.2960-2536G>C) | |
2 | g.135800674C>T | CA348592739 | LCT | c.4799G>A (p.Ser1600Asn) c.2960-2536G>A (n.2960-2536G>A) | gnomAD v4 |
2 | g.135800675T>A | CA348592741 | LCT | c.4798A>T (p.Ser1600Cys) c.2960-2537A>T (n.2960-2537A>T) | dbSNP |
2 | g.135800675T>C | CA348592743 | LCT | c.4798A>G (p.Ser1600Gly) c.2960-2537A>G (n.2960-2537A>G) | gnomAD v4 |
2 | g.135800675T>G | CA348592746 | LCT | c.4798A>C (p.Ser1600Arg) c.2960-2537A>C (n.2960-2537A>C) | |
2 | g.135800675T= | CA1290827612 | LCT | c.4798A= (p.Ser1600=) c.2960-2537A= (n.2960-2537A=) | |
2 | g.135800676G>A | CA429086379 | LCT | c.4797C>T (p.Ser1599=) c.2960-2538C>T (n.2960-2538C>T) | |
2 | g.135800676G>C | CA348592749 | LCT | c.4797C>G (p.Ser1599Arg) c.2960-2538C>G (n.2960-2538C>G) | |
2 | g.135800676G>T | CA348592753 | LCT | c.4797C>A (p.Ser1599Arg) c.2960-2538C>A (n.2960-2538C>A) | |
2 | g.135800677C>A | CA348592760 | LCT | c.4796G>T (p.Ser1599Ile) c.2960-2539G>T (n.2960-2539G>T) | gnomAD v4 |
2 | g.135800677C= | CA1290827613 | LCT | c.4796G= (p.Ser1599=) c.2960-2539G= (n.2960-2539G=) | |
2 | g.135800677C>G | CA348592763 | LCT | c.4796G>C (p.Ser1599Thr) c.2960-2539G>C (n.2960-2539G>C) | |
2 | g.135800677C>T | CA348592756 | LCT | c.4796G>A (p.Ser1599Asn) c.2960-2539G>A (n.2960-2539G>A) | dbSNP |
2 | g.135800678T>A | CA348592767 | LCT | c.4795A>T (p.Ser1599Cys) c.2960-2540A>T (n.2960-2540A>T) | |
2 | g.135800678T>C | CA348592771 | LCT | c.4795A>G (p.Ser1599Gly) c.2960-2540A>G (n.2960-2540A>G) | gnomAD v4 |
2 | g.135800678T>G | CA348592773 | LCT | c.4795A>C (p.Ser1599Arg) c.2960-2540A>C (n.2960-2540A>C) | |
2 | g.135800679G>A | CA429086381 | LCT | c.4794C>T (p.Ile1598=) c.2960-2541C>T (n.2960-2541C>T) | |
2 | g.135800679G>C | CA348592775 | LCT | c.4794C>G (p.Ile1598Met) c.2960-2541C>G (n.2960-2541C>G) | |
2 | g.135800679G= | CA1290827614 | LCT | c.4794C= (p.Ile1598=) c.2960-2541C= (n.2960-2541C=) | |
2 | g.135800679G>T | CA56606891 | LCT | c.4794C>A (p.Ile1598=) c.2960-2541C>A (n.2960-2541C>A) | dbSNP |
2 | g.135800680A>C | CA348592786 | LCT | c.4793T>G (p.Ile1598Ser) c.2960-2542T>G (n.2960-2542T>G) | |
2 | g.135800680A>G | CA348592783 | LCT | c.4793T>C (p.Ile1598Thr) c.2960-2542T>C (n.2960-2542T>C) | |
2 | g.135800680A>T | CA348592779 | LCT | c.4793T>A (p.Ile1598Asn) c.2960-2542T>A (n.2960-2542T>A) | |
2 | g.135800681T>A | CA348592791 | LCT | c.4792A>T (p.Ile1598Phe) c.2960-2543A>T (n.2960-2543A>T) | |
2 | g.135800681T>C | CA348592793 | LCT | c.4792A>G (p.Ile1598Val) c.2960-2543A>G (n.2960-2543A>G) | |
2 | g.135800681T>G | CA348592795 | LCT | c.4792A>C (p.Ile1598Leu) c.2960-2543A>C (n.2960-2543A>C) | |
2 | g.135800682G>A | CA429086382 | LCT | c.4791C>T (p.Thr1597=) c.2960-2544C>T (n.2960-2544C>T) | dbSNP |
2 | g.135800682G>C | CA1887772 | LCT | c.4791C>G (p.Thr1597=) c.2960-2544C>G (n.2960-2544C>G) | dbSNP ExAC gnomAD v2 |
2 | g.135800682G= | CA1290827615 | LCT | c.4791C= (p.Thr1597=) c.2960-2544C= (n.2960-2544C=) | |
2 | g.135800682G>T | CA429086383 | LCT | c.4791C>A (p.Thr1597=) c.2960-2544C>A (n.2960-2544C>A) | |
2 | g.135800683G>A | CA348592801 | LCT | c.4790C>T (p.Thr1597Ile) c.2960-2545C>T (n.2960-2545C>T) | |
2 | g.135800683G>C | CA348592804 | LCT | c.4790C>G (p.Thr1597Ser) c.2960-2545C>G (n.2960-2545C>G) | gnomAD v4 |
2 | g.135800683G>T | CA348592806 | LCT | c.4790C>A (p.Thr1597Asn) c.2960-2545C>A (n.2960-2545C>A) | |
2 | g.135800684T>A | CA1887773 | LCT | c.4789A>T (p.Thr1597Ser) c.2960-2546A>T (n.2960-2546A>T) | dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.135800684T>C | CA348592816 | LCT | c.4789A>G (p.Thr1597Ala) c.2960-2546A>G (n.2960-2546A>G) | dbSNP gnomAD v4 |
2 | g.135800684T>G | CA348592810 | LCT | c.4789A>C (p.Thr1597Pro) c.2960-2546A>C (n.2960-2546A>C) | |
2 | g.135800684T= | CA1290827616 | LCT | c.4789A= (p.Thr1597=) c.2960-2546A= (n.2960-2546A=) | |
2 | g.135800685G>A | CA429086384 | LCT | c.4788C>T (p.Ile1596=) c.2960-2547C>T (n.2960-2547C>T) | gnomAD v4 |
2 | g.135800685G>C | CA348592818 | LCT | c.4788C>G (p.Ile1596Met) c.2960-2547C>G (n.2960-2547C>G) | |
2 | g.135800685G>T | CA429086385 | LCT | c.4788C>A (p.Ile1596=) c.2960-2547C>A (n.2960-2547C>A) | |
2 | g.135800686A>C | CA348592820 | LCT | c.4787T>G (p.Ile1596Ser) c.2960-2548T>G (n.2960-2548T>G) | |
2 | g.135800686A>G | CA348592824 | LCT | c.4787T>C (p.Ile1596Thr) c.2960-2548T>C (n.2960-2548T>C) | |
2 | g.135800686A>T | CA348592827 | LCT | c.4787T>A (p.Ile1596Asn) c.2960-2548T>A (n.2960-2548T>A) | |
2 | g.135800687T>A | CA348592831 | LCT | c.4786A>T (p.Ile1596Phe) c.2960-2549A>T (n.2960-2549A>T) | |
2 | g.135800687T>C | CA348592833 | LCT | c.4786A>G (p.Ile1596Val) c.2960-2549A>G (n.2960-2549A>G) | gnomAD v4 |
2 | g.135800687T>G | CA348592837 | LCT | c.4786A>C (p.Ile1596Leu) c.2960-2549A>C (n.2960-2549A>C) | |
2 | g.135800688G>A | CA429086388 | LCT | c.4785C>T (p.Ser1595=) c.2960-2550C>T (n.2960-2550C>T) | dbSNP gnomAD v4 |
2 | g.135800688G>C | CA429086389 | LCT | c.4785C>G (p.Ser1595=) c.2960-2550C>G (n.2960-2550C>G) | |
2 | g.135800688G= | CA1290827617 | LCT | c.4785C= (p.Ser1595=) c.2960-2550C= (n.2960-2550C=) | |
2 | g.135800688G>T | CA429086390 | LCT | c.4785C>A (p.Ser1595=) c.2960-2550C>A (n.2960-2550C>A) | |
2 | g.135800689G>A | CA348592839 | LCT | c.4784C>T (p.Ser1595Phe) c.2960-2551C>T (n.2960-2551C>T) | |
2 | g.135800689G>C | CA348592846 | LCT | c.4784C>G (p.Ser1595Cys) c.2960-2551C>G (n.2960-2551C>G) | |
2 | g.135800689G>T | CA348592843 | LCT | c.4784C>A (p.Ser1595Tyr) c.2960-2551C>A (n.2960-2551C>A) | |
2 | g.135800690A>C | CA348592849 | LCT | c.4783T>G (p.Ser1595Ala) c.2960-2552T>G (n.2960-2552T>G) | |
2 | g.135800690A>G | CA348592852 | LCT | c.4783T>C (p.Ser1595Pro) c.2960-2552T>C (n.2960-2552T>C) | |
2 | g.135800690A>T | CA348592856 | LCT | c.4783T>A (p.Ser1595Thr) c.2960-2552T>A (n.2960-2552T>A) | |
2 | g.135800691A>C | CA348592859 | LCT | c.4782T>G (p.Ile1594Met) c.2960-2553T>G (n.2960-2553T>G) | |
2 | g.135800691A>G | CA429086392 | LCT | c.4782T>C (p.Ile1594=) c.2960-2553T>C (n.2960-2553T>C) | |
2 | g.135800691A>T | CA429086393 | LCT | c.4782T>A (p.Ile1594=) c.2960-2553T>A (n.2960-2553T>A) | |
2 | g.135800692A>C | CA348592869 | LCT | c.4781T>G (p.Ile1594Ser) c.2960-2554T>G (n.2960-2554T>G) | |
2 | g.135800692A>G | CA348592862 | LCT | c.4781T>C (p.Ile1594Thr) c.2960-2554T>C (n.2960-2554T>C) | gnomAD v4 |
2 | g.135800692A>T | CA348592865 | LCT | c.4781T>A (p.Ile1594Asn) c.2960-2554T>A (n.2960-2554T>A) | |
2 | g.135800693T>A | CA348592870 | LCT | c.4780A>T (p.Ile1594Phe) c.2960-2555A>T (n.2960-2555A>T) | |
2 | g.135800693T>C | CA348592876 | LCT | c.4780A>G (p.Ile1594Val) c.2960-2555A>G (n.2960-2555A>G) | |
2 | g.135800693T>G | CA348592878 | LCT | c.4780A>C (p.Ile1594Leu) c.2960-2555A>C (n.2960-2555A>C) | |
2 | g.135800694C>A | CA429086394 | LCT | c.4779G>T (p.Val1593=) c.2960-2556G>T (n.2960-2556G>T) | |
2 | g.135800694C>G | CA429086395 | LCT | c.4779G>C (p.Val1593=) c.2960-2556G>C (n.2960-2556G>C) | |
2 | g.135800694C>T | CA429086396 | LCT | c.4779G>A (p.Val1593=) c.2960-2556G>A (n.2960-2556G>A) | |
2 | g.135800695A>C | CA348592882 | LCT | c.4778T>G (p.Val1593Gly) c.2960-2557T>G (n.2960-2557T>G) | |
2 | g.135800695A>G | CA348592884 | LCT | c.4778T>C (p.Val1593Ala) c.2960-2557T>C (n.2960-2557T>C) | |
2 | g.135800695A>T | CA348592888 | LCT | c.4778T>A (p.Val1593Glu) c.2960-2557T>A (n.2960-2557T>A) | |
2 | g.135800696C>A | CA348592890 | LCT | c.4777G>T (p.Val1593Leu) c.2960-2558G>T (n.2960-2558G>T) | |
2 | g.135800696C= | CA1290827618 | LCT | c.4777G= (p.Val1593=) c.2960-2558G= (n.2960-2558G=) | |
2 | g.135800696C>G | CA348592894 | LCT | c.4777G>C (p.Val1593Leu) c.2960-2558G>C (n.2960-2558G>C) | dbSNP gnomAD v3 gnomAD v4 |
2 | g.135800696C>T | CA1887774 | LCT | c.4777G>A (p.Val1593Met) c.2960-2558G>A (n.2960-2558G>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135800697G>A | CA1887775 | LCT | c.4776C>T (p.Gly1592=) c.2960-2559C>T (n.2960-2559C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135800697G>C | CA429086397 | LCT | c.4776C>G (p.Gly1592=) c.2960-2559C>G (n.2960-2559C>G) | COSMIC |
2 | g.135800697G= | CA1290827619 | LCT | c.4776C= (p.Gly1592=) c.2960-2559C= (n.2960-2559C=) | |
2 | g.135800697G>T | CA429086398 | LCT | c.4776C>A (p.Gly1592=) c.2960-2559C>A (n.2960-2559C>A) | dbSNP gnomAD v2 gnomAD v4 |
2 | g.135800698C>A | CA348592900 | LCT | c.4775G>T (p.Gly1592Val) c.2960-2560G>T (n.2960-2560G>T) | COSMIC |
2 | g.135800698C>G | CA348592908 | LCT | c.4775G>C (p.Gly1592Ala) c.2960-2560G>C (n.2960-2560G>C) | |
2 | g.135800698C>T | CA348592910 | LCT | c.4775G>A (p.Gly1592Asp) c.2960-2560G>A (n.2960-2560G>A) | |
2 | g.135800699C>A | CA348592914 | LCT | c.4774G>T (p.Gly1592Cys) c.2960-2561G>T (n.2960-2561G>T) | |
2 | g.135800699C>G | CA348592918 | LCT | c.4774G>C (p.Gly1592Arg) c.2960-2561G>C (n.2960-2561G>C) | |
2 | g.135800699C>T | CA348592915 | LCT | c.4774G>A (p.Gly1592Ser) c.2960-2561G>A (n.2960-2561G>A) | |
2 | g.135800700A>C | CA429086399 | LCT | c.4773T>G (p.Gly1591=) c.2960-2562T>G (n.2960-2562T>G) | |
2 | g.135800700A>G | CA429086400 | LCT | c.4773T>C (p.Gly1591=) c.2960-2562T>C (n.2960-2562T>C) | |
2 | g.135800700A>T | CA429086401 | LCT | c.4773T>A (p.Gly1591=) c.2960-2562T>A (n.2960-2562T>A) | |
2 | g.135800701C>A | CA348592920 | LCT | c.4772G>T (p.Gly1591Val) c.2960-2563G>T (n.2960-2563G>T) | gnomAD v4 |
2 | g.135800701C= | CA1290827620 | LCT | c.4772G= (p.Gly1591=) c.2960-2563G= (n.2960-2563G=) | |
2 | g.135800701C>G | CA348592924 | LCT | c.4772G>C (p.Gly1591Ala) c.2960-2563G>C (n.2960-2563G>C) | |
2 | g.135800701C>T | CA348592927 | LCT | c.4772G>A (p.Gly1591Asp) c.2960-2563G>A (n.2960-2563G>A) | dbSNP gnomAD v3 gnomAD v4 |
2 | g.135800702C>A | CA348592928 | LCT | c.4771G>T (p.Gly1591Cys) c.2960-2564G>T (n.2960-2564G>T) | |
2 | g.135800702C>G | CA348592930 | LCT | c.4771G>C (p.Gly1591Arg) c.2960-2564G>C (n.2960-2564G>C) | COSMIC |
2 | g.135800702C>T | CA348592934 | LCT | c.4771G>A (p.Gly1591Ser) c.2960-2564G>A (n.2960-2564G>A) | |
2 | g.135800703T>A | CA348592938 | LCT | c.4770A>T (p.Gln1590His) c.2960-2565A>T (n.2960-2565A>T) | |
2 | g.135800703T>C | CA429086404 | LCT | c.4770A>G (p.Gln1590=) c.2960-2565A>G (n.2960-2565A>G) | |
2 | g.135800703T>G | CA348592940 | LCT | c.4770A>C (p.Gln1590His) c.2960-2565A>C (n.2960-2565A>C) | |
2 | g.135800704T>A | CA348592942 | LCT | c.4769A>T (p.Gln1590Leu) c.2960-2566A>T (n.2960-2566A>T) | |
2 | g.135800704T>C | CA348592945 | LCT | c.4769A>G (p.Gln1590Arg) c.2960-2566A>G (n.2960-2566A>G) | |
2 | g.135800704T>G | CA348592948 | LCT | c.4769A>C (p.Gln1590Pro) c.2960-2566A>C (n.2960-2566A>C) | |
2 | g.135800705G>A | CA348592951 | LCT | c.4768C>T (p.Gln1590Ter) c.2960-2567C>T (n.2960-2567C>T) | |
2 | g.135800705G>C | CA348592954 | LCT | c.4768C>G (p.Gln1590Glu) c.2960-2567C>G (n.2960-2567C>G) | |
2 | g.135800705G>T | CA348592956 | LCT | c.4768C>A (p.Gln1590Lys) c.2960-2567C>A (n.2960-2567C>A) | gnomAD v4 |
2 | g.135800706A>C | CA348592958 | LCT | c.4767T>G (p.Ser1589Arg) c.2960-2568T>G (n.2960-2568T>G) | |
2 | g.135800706A>G | CA429086408 | LCT | c.4767T>C (p.Ser1589=) c.2960-2568T>C (n.2960-2568T>C) | |
2 | g.135800706A>T | CA348592961 | LCT | c.4767T>A (p.Ser1589Arg) c.2960-2568T>A (n.2960-2568T>A) | |
2 | g.135800707C>A | CA348592963 | LCT | c.4766G>T (p.Ser1589Ile) c.2960-2569G>T (n.2960-2569G>T) | |
2 | g.135800707C>G | CA348592965 | LCT | c.4766G>C (p.Ser1589Thr) c.2960-2569G>C (n.2960-2569G>C) | |
2 | g.135800707C>T | CA348592967 | LCT | c.4766G>A (p.Ser1589Asn) c.2960-2569G>A (n.2960-2569G>A) | |
2 | g.135800708T>A | CA348592968 | LCT | c.4765A>T (p.Ser1589Cys) c.2960-2570A>T (n.2960-2570A>T) | |
2 | g.135800708T>C | CA348592970 | LCT | c.4765A>G (p.Ser1589Gly) c.2960-2570A>G (n.2960-2570A>G) | gnomAD v4 |
2 | g.135800708T>G | CA348592971 | LCT | c.4765A>C (p.Ser1589Arg) c.2960-2570A>C (n.2960-2570A>C) | dbSNP gnomAD v4 |
2 | g.135800708T= | CA1290827621 | LCT | c.4765A= (p.Ser1589=) c.2960-2570A= (n.2960-2570A=) | |
2 | g.135800709G>A | CA429086436 | LCT | c.4764C>T (p.Ala1588=) c.2960-2571C>T (n.2960-2571C>T) | |
2 | g.135800709G>C | CA429086437 | LCT | c.4764C>G (p.Ala1588=) c.2960-2571C>G (n.2960-2571C>G) | |
2 | g.135800709G>T | CA429086435 | LCT | c.4764C>A (p.Ala1588=) c.2960-2571C>A (n.2960-2571C>A) | |
2 | g.135800710G>A | CA348592973 | LCT | c.4763C>T (p.Ala1588Val) c.2960-2572C>T (n.2960-2572C>T) | |
2 | g.135800710G>C | CA348592975 | LCT | c.4763C>G (p.Ala1588Gly) c.2960-2572C>G (n.2960-2572C>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135800710G= | CA1290827622 | LCT | c.4763C= (p.Ala1588=) c.2960-2572C= (n.2960-2572C=) | |
2 | g.135800710G>T | CA56606905 | LCT | c.4763C>A (p.Ala1588Asp) c.2960-2572C>A (n.2960-2572C>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135800711C>A | CA348592978 | LCT | c.4762G>T (p.Ala1588Ser) c.2960-2573G>T (n.2960-2573G>T) | ClinVar |
2 | g.135800711C= | CA1290827623 | LCT | c.4762G= (p.Ala1588=) c.2960-2573G= (n.2960-2573G=) | |
2 | g.135800711C>G | CA348592979 | LCT | c.4762G>C (p.Ala1588Pro) c.2960-2573G>C (n.2960-2573G>C) | |
2 | g.135800711C>T | CA1887776 | LCT | c.4762G>A (p.Ala1588Thr) c.2960-2573G>A (n.2960-2573G>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
2 | g.135800712G>A | CA1887777 | LCT | c.4761C>T (p.Arg1587=) c.2960-2574C>T (n.2960-2574C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
2 | g.135800712G>C | CA429086438 | LCT | c.4761C>G (p.Arg1587=) c.2960-2574C>G (n.2960-2574C>G) | |
2 | g.135800712G= | CA1290827624 | LCT | c.4761C= (p.Arg1587=) c.2960-2574C= (n.2960-2574C=) | |
2 | g.135800712G>T | CA429086439 | LCT | c.4761C>A (p.Arg1587=) c.2960-2574C>A (n.2960-2574C>A) | COSMIC |
2 | g.135800713C>A | CA348592983 | LCT | c.4760G>T (p.Arg1587Leu) c.2960-2575G>T (n.2960-2575G>T) | gnomAD v4 |
2 | g.135800713C= | CA1290827625 | LCT | c.4760G= (p.Arg1587=) c.2960-2575G= (n.2960-2575G=) | |
2 | g.135800713C>G | CA348592982 | LCT | c.4760G>C (p.Arg1587Pro) c.2960-2575G>C (n.2960-2575G>C) | |
2 | g.135800713C>T | CA1887778 | LCT | c.4760G>A (p.Arg1587His) c.2960-2575G>A (n.2960-2575G>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
2 | g.135800714G>A | CA1887779 | LCT | c.4759C>T (p.Arg1587Cys) c.2960-2576C>T (n.2960-2576C>T) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
2 | g.135800714G>C | CA348592990 | LCT | c.4759C>G (p.Arg1587Gly) c.2960-2576C>G (n.2960-2576C>G) | |
2 | g.135800714G= | CA1290827626 | LCT | c.4759C= (p.Arg1587=) c.2960-2576C= (n.2960-2576C=) | |
2 | g.135800714G>T | CA348592987 | LCT | c.4759C>A (p.Arg1587Ser) c.2960-2576C>A (n.2960-2576C>A) | gnomAD v4 |
2 | g.135800715G>A | CA56606910 | LCT | c.4758C>T (p.Tyr1586=) c.2960-2577C>T (n.2960-2577C>T) | dbSNP gnomAD v3 gnomAD v4 |
2 | g.135800715G>C | CA348592994 | LCT | c.4758C>G (p.Tyr1586Ter) c.2960-2577C>G (n.2960-2577C>G) | |
2 | g.135800715G= | CA1290827627 | LCT | c.4758C= (p.Tyr1586=) c.2960-2577C= (n.2960-2577C=) | |
2 | g.135800715G>T | CA348592992 | LCT | c.4758C>A (p.Tyr1586Ter) c.2960-2577C>A (n.2960-2577C>A) | dbSNP |
2 | g.135800716T>A | CA348592996 | LCT | c.4757A>T (p.Tyr1586Phe) c.2960-2578A>T (n.2960-2578A>T) | |
2 | g.135800716T>C | CA348592998 | LCT | c.4757A>G (p.Tyr1586Cys) c.2960-2578A>G (n.2960-2578A>G) | |
2 | g.135800716T>G | CA348593001 | LCT | c.4757A>C (p.Tyr1586Ser) c.2960-2578A>C (n.2960-2578A>C) | |
2 | g.135800717A>C | CA348593007 | LCT | c.4756T>G (p.Tyr1586Asp) c.2960-2579T>G (n.2960-2579T>G) | |
2 | g.135800717A>G | CA348593008 | LCT | c.4756T>C (p.Tyr1586His) c.2960-2579T>C (n.2960-2579T>C) | COSMIC |
2 | g.135800717A>T | CA348593009 | LCT | c.4756T>A (p.Tyr1586Asn) c.2960-2579T>A (n.2960-2579T>A) | |
2 | g.135800718C>A | CA429086440 | LCT | c.4755G>T (p.Val1585=) c.2960-2580G>T (n.2960-2580G>T) | |
2 | g.135800718C= | CA1290827628 | LCT | c.4755G= (p.Val1585=) c.2960-2580G= (n.2960-2580G=) | |
2 | g.135800718C>G | CA429086441 | LCT | c.4755G>C (p.Val1585=) c.2960-2580G>C (n.2960-2580G>C) | |
2 | g.135800718C>T | CA429086442 | LCT | c.4755G>A (p.Val1585=) c.2960-2580G>A (n.2960-2580G>A) | dbSNP |
2 | g.135800719A>C | CA348593015 | LCT | c.4754T>G (p.Val1585Gly) c.2960-2581T>G (n.2960-2581T>G) | |
2 | g.135800719A>G | CA348593018 | LCT | c.4754T>C (p.Val1585Ala) c.2960-2581T>C (n.2960-2581T>C) | gnomAD v4 |
2 | g.135800719A>T | CA348593021 | LCT | c.4754T>A (p.Val1585Glu) c.2960-2581T>A (n.2960-2581T>A) | |
2 | g.135800720C>A | CA348593023 | LCT | c.4753G>T (p.Val1585Leu) c.2960-2582G>T (n.2960-2582G>T) | |
2 | g.135800720C= | CA1290827629 | LCT | c.4753G= (p.Val1585=) c.2960-2582G= (n.2960-2582G=) | |
2 | g.135800720C>G | CA348593026 | LCT | c.4753G>C (p.Val1585Leu) c.2960-2582G>C (n.2960-2582G>C) | |
2 | g.135800720C>T | CA348593028 | LCT | c.4753G>A (p.Val1585Met) c.2960-2582G>A (n.2960-2582G>A) | dbSNP gnomAD v2 gnomAD v4 |
2 | g.135800721A= | CA1290827630 | LCT | c.4752T= (p.Asp1584=) c.2960-2583T= (n.2960-2583T=) | |
2 | g.135800721A>C | CA348593033 | LCT | c.4752T>G (p.Asp1584Glu) c.2960-2583T>G (n.2960-2583T>G) | |
2 | g.135800721A>G | CA429086443 | LCT | c.4752T>C (p.Asp1584=) c.2960-2583T>C (n.2960-2583T>C) | dbSNP gnomAD v2 gnomAD v4 |
2 | g.135800721A>T | CA348593031 | LCT | c.4752T>A (p.Asp1584Glu) c.2960-2583T>A (n.2960-2583T>A) | |
2 | g.135800722T>A | CA348593036 | LCT | c.4751A>T (p.Asp1584Val) c.2960-2584A>T (n.2960-2584A>T) | |
2 | g.135800722T>C | CA348593039 | LCT | c.4751A>G (p.Asp1584Gly) c.2960-2584A>G (n.2960-2584A>G) | |
2 | g.135800722T>G | CA348593041 | LCT | c.4751A>C (p.Asp1584Ala) c.2960-2584A>C (n.2960-2584A>C) | |
2 | g.135800723C>A | CA348593042 | LCT | c.4750G>T (p.Asp1584Tyr) c.2960-2585G>T (n.2960-2585G>T) | COSMIC |
2 | g.135800723C= | CA1290827631 | LCT | c.4750G= (p.Asp1584=) c.2960-2585G= (n.2960-2585G=) | |
2 | g.135800723C>G | CA348593044 | LCT | c.4750G>C (p.Asp1584His) c.2960-2585G>C (n.2960-2585G>C) | |
2 | g.135800723C>T | CA1887780 | LCT | c.4750G>A (p.Asp1584Asn) c.2960-2585G>A (n.2960-2585G>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
2 | g.135800724G>A | CA1887781 | LCT | c.4749C>T (p.Asn1583=) c.2960-2586C>T (n.2960-2586C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
2 | g.135800724G>C | CA348593047 | LCT | c.4749C>G (p.Asn1583Lys) c.2960-2586C>G (n.2960-2586C>G) | |
2 | g.135800724G= | CA1290827632 | LCT | c.4749C= (p.Asn1583=) c.2960-2586C= (n.2960-2586C=) | |
2 | g.135800724G>T | CA348593049 | LCT | c.4749C>A (p.Asn1583Lys) c.2960-2586C>A (n.2960-2586C>A) | |
2 | g.135800725T>A | CA348593051 | LCT | c.4748A>T (p.Asn1583Ile) c.2960-2587A>T (n.2960-2587A>T) | gnomAD v4 |
2 | g.135800725T>C | CA348593053 | LCT | c.4748A>G (p.Asn1583Ser) c.2960-2587A>G (n.2960-2587A>G) | |
2 | g.135800725T>G | CA348593054 | LCT | c.4748A>C (p.Asn1583Thr) c.2960-2587A>C (n.2960-2587A>C) | |
2 | g.135800726T>A | CA348593062 | LCT | c.4747A>T (p.Asn1583Tyr) c.2960-2588A>T (n.2960-2588A>T) | |
2 | g.135800726T>C | CA348593060 | LCT | c.4747A>G (p.Asn1583Asp) c.2960-2588A>G (n.2960-2588A>G) | |
2 | g.135800726T>G | CA348593057 | LCT | c.4747A>C (p.Asn1583His) c.2960-2588A>C (n.2960-2588A>C) | |
2 | g.135800727G>A | CA429086444 | LCT | c.4746C>T (p.Tyr1582=) c.2960-2589C>T (n.2960-2589C>T) | ClinVar dbSNP gnomAD v4 |
2 | g.135800727G>C | CA348593070 | LCT | c.4746C>G (p.Tyr1582Ter) c.2960-2589C>G (n.2960-2589C>G) | |
2 | g.135800727G= | CA1290827633 | LCT | c.4746C= (p.Tyr1582=) c.2960-2589C= (n.2960-2589C=) | |
2 | g.135800727G>T | CA348593066 | LCT | c.4746C>A (p.Tyr1582Ter) c.2960-2589C>A (n.2960-2589C>A) | |
2 | g.135800728T>A | CA348593072 | LCT | c.4745A>T (p.Tyr1582Phe) c.2960-2590A>T (n.2960-2590A>T) | |
2 | g.135800728T>C | CA348593073 | LCT | c.4745A>G (p.Tyr1582Cys) c.2960-2590A>G (n.2960-2590A>G) | |
2 | g.135800728T>G | CA348593076 | LCT | c.4745A>C (p.Tyr1582Ser) c.2960-2590A>C (n.2960-2590A>C) | |
2 | g.135800729A>C | CA348593078 | LCT | c.4744T>G (p.Tyr1582Asp) c.2960-2591T>G (n.2960-2591T>G) | |
2 | g.135800729A>G | CA348593080 | LCT | c.4744T>C (p.Tyr1582His) c.2960-2591T>C (n.2960-2591T>C) | |
2 | g.135800729A>T | CA348593083 | LCT | c.4744T>A (p.Tyr1582Asn) c.2960-2591T>A (n.2960-2591T>A) | |
2 | g.135800730C>A | CA429086445 | LCT | c.4743G>T (p.Leu1581=) c.2960-2592G>T (n.2960-2592G>T) | |
2 | g.135800730C>G | CA429086446 | LCT | c.4743G>C (p.Leu1581=) c.2960-2592G>C (n.2960-2592G>C) | |
2 | g.135800730C>T | CA429086447 | LCT | c.4743G>A (p.Leu1581=) c.2960-2592G>A (n.2960-2592G>A) | gnomAD v4 |
2 | g.135800731A>C | CA348593085 | LCT | c.4742T>G (p.Leu1581Arg) c.2960-2593T>G (n.2960-2593T>G) | |
2 | g.135800731A>G | CA348593087 | LCT | c.4742T>C (p.Leu1581Pro) c.2960-2593T>C (n.2960-2593T>C) | gnomAD v4 |
2 | g.135800731A>T | CA348593086 | LCT | c.4742T>A (p.Leu1581Gln) c.2960-2593T>A (n.2960-2593T>A) | |
2 | g.135800731_135800734dup | CA2661274838 | LCT | c.4739_4742dup (p.Tyr1582SerfsTer21) c.2960-2596_2960-2593dup (n.2960-2596_2960-2593dup) | gnomAD v4 |
2 | g.135800732G>A | CA429086448 | LCT | c.4741C>T (p.Leu1581=) c.2960-2594C>T (n.2960-2594C>T) | |
2 | g.135800732G>C | CA348593090 | LCT | c.4741C>G (p.Leu1581Val) c.2960-2594C>G (n.2960-2594C>G) | |
2 | g.135800732G>T | CA348593093 | LCT | c.4741C>A (p.Leu1581Met) c.2960-2594C>A (n.2960-2594C>A) | |
2 | g.135800733A>C | CA348593095 | LCT | c.4740T>G (p.His1580Gln) c.2960-2595T>G (n.2960-2595T>G) | |
2 | g.135800733A>G | CA429086449 | LCT | c.4740T>C (p.His1580=) c.2960-2595T>C (n.2960-2595T>C) | |
2 | g.135800733A>T | CA348593098 | LCT | c.4740T>A (p.His1580Gln) c.2960-2595T>A (n.2960-2595T>A) | |
2 | g.135800734T>A | CA348593099 | LCT | c.4739A>T (p.His1580Leu) c.2960-2596A>T (n.2960-2596A>T) | |
2 | g.135800734T>C | CA348593104 | LCT | c.4739A>G (p.His1580Arg) c.2960-2596A>G (n.2960-2596A>G) | gnomAD v4 |
2 | g.135800734T>G | CA348593101 | LCT | c.4739A>C (p.His1580Pro) c.2960-2596A>C (n.2960-2596A>C) | |
2 | g.135800735G>A | CA348593106 | LCT | c.4738C>T (p.His1580Tyr) c.2960-2597C>T (n.2960-2597C>T) | |
2 | g.135800735G>C | CA348593107 | LCT | c.4738C>G (p.His1580Asp) c.2960-2597C>G (n.2960-2597C>G) | |
2 | g.135800735G>T | CA348593109 | LCT | c.4738C>A (p.His1580Asn) c.2960-2597C>A (n.2960-2597C>A) | gnomAD v4 |
2 | g.135800736C>A | CA348593110 | LCT | c.4737G>T (p.Trp1579Cys) c.2960-2598G>T (n.2960-2598G>T) | |
2 | g.135800736C>G | CA348593112 | LCT | c.4737G>C (p.Trp1579Cys) c.2960-2598G>C (n.2960-2598G>C) | |
2 | g.135800736C>T | CA348593113 | LCT | c.4737G>A (p.Trp1579Ter) c.2960-2598G>A (n.2960-2598G>A) | |
2 | g.135800737C>A | CA348593115 | LCT | c.4736G>T (p.Trp1579Leu) c.2960-2599G>T (n.2960-2599G>T) | |
2 | g.135800737C>G | CA348593118 | LCT | c.4736G>C (p.Trp1579Ser) c.2960-2599G>C (n.2960-2599G>C) | |
2 | g.135800737C>T | CA348593121 | LCT | c.4736G>A (p.Trp1579Ter) c.2960-2599G>A (n.2960-2599G>A) | |
2 | g.135800738A>C | CA348593127 | LCT | c.4735T>G (p.Trp1579Gly) c.2960-2600T>G (n.2960-2600T>G) | |
2 | g.135800738A>G | CA348593129 | LCT | c.4735T>C (p.Trp1579Arg) c.2960-2600T>C (n.2960-2600T>C) | |
2 | g.135800738A>T | CA348593131 | LCT | c.4735T>A (p.Trp1579Arg) c.2960-2600T>A (n.2960-2600T>A) | |
2 | g.135800739G>A | CA429086450 | LCT | c.4734C>T (p.Ala1578=) c.2960-2601C>T (n.2960-2601C>T) | dbSNP |
2 | g.135800739G>C | CA429086451 | LCT | c.4734C>G (p.Ala1578=) c.2960-2601C>G (n.2960-2601C>G) | gnomAD v4 |
2 | g.135800739G= | CA1290827634 | LCT | c.4734C= (p.Ala1578=) c.2960-2601C= (n.2960-2601C=) | |
2 | g.135800739G>T | CA429086452 | LCT | c.4734C>A (p.Ala1578=) c.2960-2601C>A (n.2960-2601C>A) | |
2 | g.135800740G>A | CA1887782 | LCT | c.4733C>T (p.Ala1578Val) c.2960-2602C>T (n.2960-2602C>T) | dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.135800740G>C | CA348593136 | LCT | c.4733C>G (p.Ala1578Gly) c.2960-2602C>G (n.2960-2602C>G) | gnomAD v4 |
2 | g.135800740G= | CA1290827635 | LCT | c.4733C= (p.Ala1578=) c.2960-2602C= (n.2960-2602C=) | |
2 | g.135800740G>T | CA348593133 | LCT | c.4733C>A (p.Ala1578Asp) c.2960-2602C>A (n.2960-2602C>A) | gnomAD v4 |
2 | g.135800741C>A | CA348593139 | LCT | c.4732G>T (p.Ala1578Ser) c.2960-2603G>T (n.2960-2603G>T) | |
2 | g.135800741C>G | CA348593144 | LCT | c.4732G>C (p.Ala1578Pro) c.2960-2603G>C (n.2960-2603G>C) | |
2 | g.135800741C>T | CA348593142 | LCT | c.4732G>A (p.Ala1578Thr) c.2960-2603G>A (n.2960-2603G>A) | gnomAD v4 |
2 | g.135800742C>A | CA348593147 | LCT | c.4731G>T (p.Glu1577Asp) c.2960-2604G>T (n.2960-2604G>T) | |
2 | g.135800742C>G | CA348593150 | LCT | c.4731G>C (p.Glu1577Asp) c.2960-2604G>C (n.2960-2604G>C) | |
2 | g.135800742C>T | CA429086453 | LCT | c.4731G>A (p.Glu1577=) c.2960-2604G>A (n.2960-2604G>A) | |
2 | g.135800743T>A | CA348593153 | LCT | c.4730A>T (p.Glu1577Val) c.2960-2605A>T (n.2960-2605A>T) | |
2 | g.135800743T>C | CA348593155 | LCT | c.4730A>G (p.Glu1577Gly) c.2960-2605A>G (n.2960-2605A>G) | |
2 | g.135800743T>G | CA348593156 | LCT | c.4730A>C (p.Glu1577Ala) c.2960-2605A>C (n.2960-2605A>C) | |
2 | g.135800744C>A | CA348593160 | LCT | c.4729G>T (p.Glu1577Ter) c.2960-2606G>T (n.2960-2606G>T) | |
2 | g.135800744C= | CA1290827636 | LCT | c.4729G= (p.Glu1577=) c.2960-2606G= (n.2960-2606G=) | |
2 | g.135800744C>G | CA348593163 | LCT | c.4729G>C (p.Glu1577Gln) c.2960-2606G>C (n.2960-2606G>C) | dbSNP |
2 | g.135800744C>T | CA348593165 | LCT | c.4729G>A (p.Glu1577Lys) c.2960-2606G>A (n.2960-2606G>A) | |
2 | g.135800745A= | CA1290827637 | LCT | c.4728T= (p.Ala1576=) c.2960-2607T= (n.2960-2607T=) | |
2 | g.135800745A>C | CA429086454 | LCT | c.4728T>G (p.Ala1576=) c.2960-2607T>G (n.2960-2607T>G) | |
2 | g.135800745A>G | CA429086455 | LCT | c.4728T>C (p.Ala1576=) c.2960-2607T>C (n.2960-2607T>C) | |
2 | g.135800745A>T | CA429086456 | LCT | c.4728T>A (p.Ala1576=) c.2960-2607T>A (n.2960-2607T>A) | |
2 | g.135800746G>A | CA348593168 | LCT | c.4727C>T (p.Ala1576Val) c.2960-2608C>T (n.2960-2608C>T) | gnomAD v4 COSMIC |
2 | g.135800746G>C | CA348593170 | LCT | c.4727C>G (p.Ala1576Gly) c.2960-2608C>G (n.2960-2608C>G) | |
2 | g.135800746G>T | CA348593173 | LCT | c.4727C>A (p.Ala1576Asp) c.2960-2608C>A (n.2960-2608C>A) | |
2 | g.135800747_135800784dup | CA536394701 | LCT | c.4690_4727dup (p.Glu1577ProfsTer8) c.2960-2645_2960-2608dup (n.2960-2645_2960-2608dup) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135800747C>A | CA348593176 | LCT | c.4726G>T (p.Ala1576Ser) c.2960-2609G>T (n.2960-2609G>T) | |
2 | g.135800747C>G | CA348593178 | LCT | c.4726G>C (p.Ala1576Pro) c.2960-2609G>C (n.2960-2609G>C) | |
2 | g.135800747C>T | CA348593179 | LCT | c.4726G>A (p.Ala1576Thr) c.2960-2609G>A (n.2960-2609G>A) | |
2 | g.135800748A>C | CA348593183 | LCT | c.4725T>G (p.His1575Gln) c.2960-2610T>G (n.2960-2610T>G) | |
2 | g.135800748A>G | CA429086457 | LCT | c.4725T>C (p.His1575=) c.2960-2610T>C (n.2960-2610T>C) | gnomAD v4 |
2 | g.135800748A>T | CA348593185 | LCT | c.4725T>A (p.His1575Gln) c.2960-2610T>A (n.2960-2610T>A) | |
2 | g.135800749T>A | CA348593187 | LCT | c.4724A>T (p.His1575Leu) c.2960-2611A>T (n.2960-2611A>T) | |
2 | g.135800749T>C | CA348593189 | LCT | c.4724A>G (p.His1575Arg) c.2960-2611A>G (n.2960-2611A>G) | |
2 | g.135800749T>G | CA348593192 | LCT | c.4724A>C (p.His1575Pro) c.2960-2611A>C (n.2960-2611A>C) | |
2 | g.135800750G>A | CA1887783 | LCT | c.4723C>T (p.His1575Tyr) c.2960-2612C>T (n.2960-2612C>T) | dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.135800750G>C | CA348593195 | LCT | c.4723C>G (p.His1575Asp) c.2960-2612C>G (n.2960-2612C>G) | |
2 | g.135800750G= | CA1290827638 | LCT | c.4723C= (p.His1575=) c.2960-2612C= (n.2960-2612C=) | |
2 | g.135800750G>T | CA348593198 | LCT | c.4723C>A (p.His1575Asn) c.2960-2612C>A (n.2960-2612C>A) | |
2 | g.135800751A>C | CA429086460 | LCT | c.4722T>G (p.Ala1574=) c.2960-2613T>G (n.2960-2613T>G) | |
2 | g.135800751A>G | CA429086458 | LCT | c.4722T>C (p.Ala1574=) c.2960-2613T>C (n.2960-2613T>C) | |
2 | g.135800751A>T | CA429086459 | LCT | c.4722T>A (p.Ala1574=) c.2960-2613T>A (n.2960-2613T>A) | |
2 | g.135800752G>A | CA348593200 | LCT | c.4721C>T (p.Ala1574Val) c.2960-2614C>T (n.2960-2614C>T) | gnomAD v4 |
2 | g.135800752G>C | CA348593204 | LCT | c.4721C>G (p.Ala1574Gly) c.2960-2614C>G (n.2960-2614C>G) | |
2 | g.135800752G>T | CA348593210 | LCT | c.4721C>A (p.Ala1574Asp) c.2960-2614C>A (n.2960-2614C>A) | |
2 | g.135800753C>A | CA348593213 | LCT | c.4720G>T (p.Ala1574Ser) c.2960-2615G>T (n.2960-2615G>T) | gnomAD v4 |
2 | g.135800753C>G | CA348593214 | LCT | c.4720G>C (p.Ala1574Pro) c.2960-2615G>C (n.2960-2615G>C) | gnomAD v4 |
2 | g.135800753C>T | CA348593217 | LCT | c.4720G>A (p.Ala1574Thr) c.2960-2615G>A (n.2960-2615G>A) | |
2 | g.135800754C>A | CA348593220 | LCT | c.4719G>T (p.Lys1573Asn) c.2960-2616G>T (n.2960-2616G>T) | |
2 | g.135800754C>G | CA348593222 | LCT | c.4719G>C (p.Lys1573Asn) c.2960-2616G>C (n.2960-2616G>C) | |
2 | g.135800754C>T | CA429086461 | LCT | c.4719G>A (p.Lys1573=) c.2960-2616G>A (n.2960-2616G>A) | |
2 | g.135800755T>A | CA348593225 | LCT | c.4718A>T (p.Lys1573Met) c.2960-2617A>T (n.2960-2617A>T) | |
2 | g.135800755T>C | CA348593228 | LCT | c.4718A>G (p.Lys1573Arg) c.2960-2617A>G (n.2960-2617A>G) | |
2 | g.135800755T>G | CA348593229 | LCT | c.4718A>C (p.Lys1573Thr) c.2960-2617A>C (n.2960-2617A>C) | |
2 | g.135800756T>A | CA348593232 | LCT | c.4717A>T (p.Lys1573Ter) c.2960-2618A>T (n.2960-2618A>T) | |
2 | g.135800756T>C | CA348593234 | LCT | c.4717A>G (p.Lys1573Glu) c.2960-2618A>G (n.2960-2618A>G) | |
2 | g.135800756T>G | CA348593237 | LCT | c.4717A>C (p.Lys1573Gln) c.2960-2618A>C (n.2960-2618A>C) | |
2 | g.135800757T>A | CA429086463 | LCT | c.4716A>T (p.Ile1572=) c.2960-2619A>T (n.2960-2619A>T) | |
2 | g.135800757T>C | CA348593239 | LCT | c.4716A>G (p.Ile1572Met) c.2960-2619A>G (n.2960-2619A>G) | dbSNP gnomAD v2 gnomAD v4 |
2 | g.135800757T>G | CA429086462 | LCT | c.4716A>C (p.Ile1572=) c.2960-2619A>C (n.2960-2619A>C) | dbSNP gnomAD v4 |
2 | g.135800757T= | CA1290827639 | LCT | c.4716A= (p.Ile1572=) c.2960-2619A= (n.2960-2619A=) |