Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
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=) | |
2 | g.135800758A>C | CA348593241 | LCT | c.4715T>G (p.Ile1572Arg) c.2960-2620T>G (n.2960-2620T>G) | |
2 | g.135800758A>G | CA348593244 | LCT | c.4715T>C (p.Ile1572Thr) c.2960-2620T>C (n.2960-2620T>C) | |
2 | g.135800758A>T | CA348593247 | LCT | c.4715T>A (p.Ile1572Lys) c.2960-2620T>A (n.2960-2620T>A) | |
2 | g.135800759T>A | CA1887784 | LCT | c.4714A>T (p.Ile1572Leu) c.2960-2621A>T (n.2960-2621A>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
2 | g.135800759T>C | CA348593251 | LCT | c.4714A>G (p.Ile1572Val) c.2960-2621A>G (n.2960-2621A>G) | |
2 | g.135800759T>G | CA348593254 | LCT | c.4714A>C (p.Ile1572Leu) c.2960-2621A>C (n.2960-2621A>C) | |
2 | g.135800759T= | CA1290827640 | LCT | c.4714A= (p.Ile1572=) c.2960-2621A= (n.2960-2621A=) | |
2 | g.135800760T>A | CA429086464 | LCT | c.4713A>T (p.Leu1571=) c.2960-2622A>T (n.2960-2622A>T) | |
2 | g.135800760T>C | CA429086465 | LCT | c.4713A>G (p.Leu1571=) c.2960-2622A>G (n.2960-2622A>G) | |
2 | g.135800760T>G | CA429086466 | LCT | c.4713A>C (p.Leu1571=) c.2960-2622A>C (n.2960-2622A>C) | |
2 | g.135800761A>C | CA348593261 | LCT | c.4712T>G (p.Leu1571Arg) c.2960-2623T>G (n.2960-2623T>G) | |
2 | g.135800761A>G | CA348593257 | LCT | c.4712T>C (p.Leu1571Pro) c.2960-2623T>C (n.2960-2623T>C) | |
2 | g.135800761A>T | CA348593260 | LCT | c.4712T>A (p.Leu1571Gln) c.2960-2623T>A (n.2960-2623T>A) | |
2 | g.135800762G>A | CA429086467 | LCT | c.4711C>T (p.Leu1571=) c.2960-2624C>T (n.2960-2624C>T) | |
2 | g.135800762G>C | CA348593263 | LCT | c.4711C>G (p.Leu1571Val) c.2960-2624C>G (n.2960-2624C>G) | |
2 | g.135800762G>T | CA348593265 | LCT | c.4711C>A (p.Leu1571Ile) c.2960-2624C>A (n.2960-2624C>A) | |
2 | g.135800763A= | CA1290827641 | LCT | c.4710T= (p.Asn1570=) c.2960-2625T= (n.2960-2625T=) | |
2 | g.135800763A>C | CA348593268 | LCT | c.4710T>G (p.Asn1570Lys) c.2960-2625T>G (n.2960-2625T>G) | |
2 | g.135800763A>G | CA429086468 | LCT | c.4710T>C (p.Asn1570=) c.2960-2625T>C (n.2960-2625T>C) | dbSNP |
2 | g.135800763A>T | CA348593270 | LCT | c.4710T>A (p.Asn1570Lys) c.2960-2625T>A (n.2960-2625T>A) | |
2 | g.135800764T>A | CA348593274 | LCT | c.4709A>T (p.Asn1570Ile) c.2960-2626A>T (n.2960-2626A>T) | |
2 | g.135800764T>C | CA348593276 | LCT | c.4709A>G (p.Asn1570Ser) c.2960-2626A>G (n.2960-2626A>G) | gnomAD v4 |
2 | g.135800764T>G | CA348593277 | LCT | c.4709A>C (p.Asn1570Thr) c.2960-2626A>C (n.2960-2626A>C) | |
2 | g.135800765T>A | CA348593280 | LCT | c.4708A>T (p.Asn1570Tyr) c.2960-2627A>T (n.2960-2627A>T) | |
2 | g.135800765T>C | CA348593281 | LCT | c.4708A>G (p.Asn1570Asp) c.2960-2627A>G (n.2960-2627A>G) | |
2 | g.135800765T>G | CA348593283 | LCT | c.4708A>C (p.Asn1570His) c.2960-2627A>C (n.2960-2627A>C) | gnomAD v4 |
2 | g.135800766G>A | CA429086469 | LCT | c.4707C>T (p.His1569=) c.2960-2628C>T (n.2960-2628C>T) | gnomAD v4 |
2 | g.135800766G>C | CA348593284 | LCT | c.4707C>G (p.His1569Gln) c.2960-2628C>G (n.2960-2628C>G) | |
2 | g.135800766G>T | CA348593287 | LCT | c.4707C>A (p.His1569Gln) c.2960-2628C>A (n.2960-2628C>A) | |
2 | g.135800767T>A | CA348593290 | LCT | c.4706A>T (p.His1569Leu) c.2960-2629A>T (n.2960-2629A>T) | |
2 | g.135800767T>C | CA348593294 | LCT | c.4706A>G (p.His1569Arg) c.2960-2629A>G (n.2960-2629A>G) | |
2 | g.135800767T>G | CA348593291 | LCT | c.4706A>C (p.His1569Pro) c.2960-2629A>C (n.2960-2629A>C) | |
2 | g.135800768G>A | CA348593296 | LCT | c.4705C>T (p.His1569Tyr) c.2960-2630C>T (n.2960-2630C>T) | gnomAD v4 |
2 | g.135800768G>C | CA348593300 | LCT | c.4705C>G (p.His1569Asp) c.2960-2630C>G (n.2960-2630C>G) | |
2 | g.135800768G>T | CA348593299 | LCT | c.4705C>A (p.His1569Asn) c.2960-2630C>A (n.2960-2630C>A) | gnomAD v4 |
2 | g.135800769G>A | CA429086470 | LCT | c.4704C>T (p.Gly1568=) c.2960-2631C>T (n.2960-2631C>T) | |
2 | g.135800769G>C | CA429086471 | LCT | c.4704C>G (p.Gly1568=) c.2960-2631C>G (n.2960-2631C>G) | |
2 | g.135800769G>T | CA429086472 | LCT | c.4704C>A (p.Gly1568=) c.2960-2631C>A (n.2960-2631C>A) | |
2 | g.135800770C>A | CA348593303 | LCT | c.4703G>T (p.Gly1568Val) c.2960-2632G>T (n.2960-2632G>T) | |
2 | g.135800770C= | CA1290827642 | LCT | c.4703G= (p.Gly1568=) c.2960-2632G= (n.2960-2632G=) | |
2 | g.135800770C>G | CA348593309 | LCT | c.4703G>C (p.Gly1568Ala) c.2960-2632G>C (n.2960-2632G>C) | |
2 | g.135800770C>T | CA348593305 | LCT | c.4703G>A (p.Gly1568Asp) c.2960-2632G>A (n.2960-2632G>A) | dbSNP gnomAD v2 gnomAD v4 |
2 | g.135800771C>A | CA348593310 | LCT | c.4702G>T (p.Gly1568Cys) c.2960-2633G>T (n.2960-2633G>T) | |
2 | g.135800771C= | CA1290827643 | LCT | c.4702G= (p.Gly1568=) c.2960-2633G= (n.2960-2633G=) | |
2 | g.135800771C>G | CA348593312 | LCT | c.4702G>C (p.Gly1568Arg) c.2960-2633G>C (n.2960-2633G>C) | |
2 | g.135800771C>T | CA56606941 | LCT | c.4702G>A (p.Gly1568Ser) c.2960-2633G>A (n.2960-2633G>A) | dbSNP gnomAD v3 gnomAD v4 |
2 | g.135800772A>C | CA429086474 | LCT | c.4701T>G (p.Val1567=) c.2960-2634T>G (n.2960-2634T>G) | gnomAD v4 |
2 | g.135800772A>G | CA429086473 | LCT | c.4701T>C (p.Val1567=) c.2960-2634T>C (n.2960-2634T>C) | |
2 | g.135800772A>T | CA429086475 | LCT | c.4701T>A (p.Val1567=) c.2960-2634T>A (n.2960-2634T>A) | |
2 | g.135800773A= | CA1290827644 | LCT | c.4700T= (p.Val1567=) c.2960-2635T= (n.2960-2635T=) | |
2 | g.135800773A>C | CA348593317 | LCT | c.4700T>G (p.Val1567Gly) c.2960-2635T>G (n.2960-2635T>G) | |
2 | g.135800773A>G | CA56606946 | LCT | c.4700T>C (p.Val1567Ala) c.2960-2635T>C (n.2960-2635T>C) | dbSNP |
2 | g.135800773A>T | CA348593320 | LCT | c.4700T>A (p.Val1567Asp) c.2960-2635T>A (n.2960-2635T>A) | |
2 | g.135800774C>A | CA348593325 | LCT | c.4699G>T (p.Val1567Phe) c.2960-2636G>T (n.2960-2636G>T) | gnomAD v4 |
2 | g.135800774C>G | CA348593327 | LCT | c.4699G>C (p.Val1567Leu) c.2960-2636G>C (n.2960-2636G>C) | |
2 | g.135800774C>T | CA348593329 | LCT | c.4699G>A (p.Val1567Ile) c.2960-2636G>A (n.2960-2636G>A) | |
2 | g.135800775A= | CA1290827645 | LCT | c.4698T= (p.Ile1566=) c.2960-2637T= (n.2960-2637T=) | |
2 | g.135800775A>C | CA1887785 | LCT | c.4698T>G (p.Ile1566Met) c.2960-2637T>G (n.2960-2637T>G) | dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.135800775A>G | CA429086476 | LCT | c.4698T>C (p.Ile1566=) c.2960-2637T>C (n.2960-2637T>C) | |
2 | g.135800775A>T | CA429086477 | LCT | c.4698T>A (p.Ile1566=) c.2960-2637T>A (n.2960-2637T>A) | |
2 | g.135800776A= | CA1290827646 | LCT | c.4697T= (p.Ile1566=) c.2960-2638T= (n.2960-2638T=) | |
2 | g.135800776A>C | CA348593338 | LCT | c.4697T>G (p.Ile1566Ser) c.2960-2638T>G (n.2960-2638T>G) | |
2 | g.135800776A>G | CA348593335 | LCT | c.4697T>C (p.Ile1566Thr) c.2960-2638T>C (n.2960-2638T>C) | dbSNP gnomAD v4 |
2 | g.135800776A>T | CA348593333 | LCT | c.4697T>A (p.Ile1566Asn) c.2960-2638T>A (n.2960-2638T>A) | |
2 | g.135800777T>A | CA348593340 | LCT | c.4696A>T (p.Ile1566Phe) c.2960-2639A>T (n.2960-2639A>T) | |
2 | g.135800777T>C | CA1887786 | LCT | c.4696A>G (p.Ile1566Val) c.2960-2639A>G (n.2960-2639A>G) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135800777T>G | CA348593345 | LCT | c.4696A>C (p.Ile1566Leu) c.2960-2639A>C (n.2960-2639A>C) | dbSNP gnomAD v2 gnomAD v4 |
2 | g.135800777T= | CA1290827647 | LCT | c.4696A= (p.Ile1566=) c.2960-2639A= (n.2960-2639A=) | |
2 | g.135800778G>A | CA10610769 | LCT | c.4695C>T (p.Tyr1565=) c.2960-2640C>T (n.2960-2640C>T) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
2 | g.135800778G>C | CA348593348 | LCT | c.4695C>G (p.Tyr1565Ter) c.2960-2640C>G (n.2960-2640C>G) | |
2 | g.135800778G= | CA1290827648 | LCT | c.4695C= (p.Tyr1565=) c.2960-2640C= (n.2960-2640C=) | |
2 | g.135800778G>T | CA348593350 | LCT | c.4695C>A (p.Tyr1565Ter) c.2960-2640C>A (n.2960-2640C>A) | |
2 | g.135800779T>A | CA348593354 | LCT | c.4694A>T (p.Tyr1565Phe) c.2960-2641A>T (n.2960-2641A>T) | |
2 | g.135800779T>C | CA348593355 | LCT | c.4694A>G (p.Tyr1565Cys) c.2960-2641A>G (n.2960-2641A>G) | |
2 | g.135800779T>G | CA348593357 | LCT | c.4694A>C (p.Tyr1565Ser) c.2960-2641A>C (n.2960-2641A>C) | |
2 | g.135800779_135800780insG | CA645528838 | LCT | c.4693_4694insC (p.Tyr1565SerfsTer13) c.2960-2642_2960-2641insC (n.2960-2642_2960-2641insC) | COSMIC |
2 | g.135800780A= | CA1290827649 | LCT | c.4693T= (p.Tyr1565=) c.2960-2642T= (n.2960-2642T=) | |
2 | g.135800780A>C | CA348593358 | LCT | c.4693T>G (p.Tyr1565Asp) c.2960-2642T>G (n.2960-2642T>G) | |
2 | g.135800780A>G | CA348593361 | LCT | c.4693T>C (p.Tyr1565His) c.2960-2642T>C (n.2960-2642T>C) | |
2 | g.135800780A>T | CA348593364 | LCT | c.4693T>A (p.Tyr1565Asn) c.2960-2642T>A (n.2960-2642T>A) | dbSNP gnomAD v2 gnomAD v4 |
2 | g.135800781G>A | CA429086480 | LCT | c.4692C>T (p.Pro1564=) c.2960-2643C>T (n.2960-2643C>T) | |
2 | g.135800781G>C | CA429086479 | LCT | c.4692C>G (p.Pro1564=) c.2960-2643C>G (n.2960-2643C>G) | dbSNP |
2 | g.135800781G>T | CA429086478 | LCT | c.4692C>A (p.Pro1564=) c.2960-2643C>A (n.2960-2643C>A) | |
2 | g.135800785dup | CA1887787 | LCT | c.4692dup (p.Tyr1565LeufsTer13) c.2960-2643dup (n.2960-2643dup) | dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.135800782G>A | CA348593373 | LCT | c.4691C>T (p.Pro1564Leu) c.2960-2644C>T (n.2960-2644C>T) | gnomAD v4 |
2 | g.135800782G>C | CA348593369 | LCT | c.4691C>G (p.Pro1564Arg) c.2960-2644C>G (n.2960-2644C>G) | |
2 | g.135800782G>T | CA348593371 | LCT | c.4691C>A (p.Pro1564His) c.2960-2644C>A (n.2960-2644C>A) | |
2 | g.135800783G>A | CA348593377 | LCT | c.4690C>T (p.Pro1564Ser) c.2960-2645C>T (n.2960-2645C>T) | |
2 | g.135800783G>C | CA348593378 | LCT | c.4690C>G (p.Pro1564Ala) c.2960-2645C>G (n.2960-2645C>G) | |
2 | g.135800783G>T | CA348593382 | LCT | c.4690C>A (p.Pro1564Thr) c.2960-2645C>A (n.2960-2645C>A) | |
2 | g.135800784G>A | CA429086481 | LCT | c.4689C>T (p.Ala1563=) c.2960-2646C>T (n.2960-2646C>T) | |
2 | g.135800784G>C | CA429086482 | LCT | c.4689C>G (p.Ala1563=) c.2960-2646C>G (n.2960-2646C>G) | |
2 | g.135800784G>T | CA429086483 | LCT | c.4689C>A (p.Ala1563=) c.2960-2646C>A (n.2960-2646C>A) | gnomAD v4 |
2 | g.135800785G>A | CA1887788 | LCT | c.4688C>T (p.Ala1563Val) c.2960-2647C>T (n.2960-2647C>T) | dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.135800785G>C | CA348593386 | LCT | c.4688C>G (p.Ala1563Gly) c.2960-2647C>G (n.2960-2647C>G) | |
2 | g.135800785G= | CA1290827650 | LCT | c.4688C= (p.Ala1563=) c.2960-2647C= (n.2960-2647C=) | |
2 | g.135800785G>T | CA348593387 | LCT | c.4688C>A (p.Ala1563Asp) c.2960-2647C>A (n.2960-2647C>A) | |
2 | g.135800786C>A | CA348593389 | LCT | c.4687G>T (p.Ala1563Ser) c.2960-2648G>T (n.2960-2648G>T) | |
2 | g.135800786C>G | CA348593391 | LCT | c.4687G>C (p.Ala1563Pro) c.2960-2648G>C (n.2960-2648G>C) | |
2 | g.135800786C>T | CA348593394 | LCT | c.4687G>A (p.Ala1563Thr) c.2960-2648G>A (n.2960-2648G>A) |