Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.135798108A>C | CA348590988 | LCT | c.4897T>G (p.Phe1633Val) c.2990T>G (p.Phe997Cys) | |
2 | g.135798108A>G | CA348590990 | LCT | c.4897T>C (p.Phe1633Leu) c.2990T>C (p.Phe997Ser) | |
2 | g.135798108A>T | CA348590989 | LCT | c.4897T>A (p.Phe1633Ile) c.2990T>A (p.Phe997Tyr) | |
2 | g.135798109A>C | CA348590991 | LCT | c.4896T>G (p.Ile1632Met) c.2989T>G (p.Phe997Val) | |
2 | g.135798109A>G | CA429086220 | LCT | c.4896T>C (p.Ile1632=) c.2989T>C (p.Phe997Leu) | |
2 | g.135798109A>T | CA429086219 | LCT | c.4896T>A (p.Ile1632=) c.2989T>A (p.Phe997Ile) | |
2 | g.135798110A>C | CA348590992 | LCT | c.4895T>G (p.Ile1632Ser) c.2988T>G (p.Tyr996Ter) | |
2 | g.135798110A>G | CA348590993 | LCT | c.4895T>C (p.Ile1632Thr) c.2988T>C (p.Tyr996=) | |
2 | g.135798110A>T | CA348590994 | LCT | c.4895T>A (p.Ile1632Asn) c.2988T>A (p.Tyr996Ter) | |
2 | g.135798111T>A | CA348590995 | LCT | c.4894A>T (p.Ile1632Phe) c.2987A>T (p.Tyr996Phe) | |
2 | g.135798111T>C | CA1887742 | LCT | c.4894A>G (p.Ile1632Val) c.2987A>G (p.Tyr996Cys) | dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.135798111T>G | CA348590996 | LCT | c.4894A>C (p.Ile1632Leu) c.2987A>C (p.Tyr996Ser) | |
2 | g.135798111T= | CA1290826533 | LCT | c.4894A= (p.Ile1632=) c.2987A= (p.Tyr996=) | |
2 | g.135798112A>C | CA429086223 | LCT | c.4893T>G (p.Pro1631=) c.2986T>G (p.Tyr996Asp) | |
2 | g.135798112A>G | CA429086224 | LCT | c.4893T>C (p.Pro1631=) c.2986T>C (p.Tyr996His) | |
2 | g.135798112A>T | CA429086225 | LCT | c.4893T>A (p.Pro1631=) c.2986T>A (p.Tyr996Asn) | |
2 | g.135798113G>A | CA348590997 | LCT | c.4892C>T (p.Pro1631Leu) c.2985C>T (p.Ser995=) | |
2 | g.135798113G>C | CA348590998 | LCT | c.4892C>G (p.Pro1631Arg) c.2985C>G (p.Ser995=) | |
2 | g.135798113G>T | CA348590999 | LCT | c.4892C>A (p.Pro1631His) c.2985C>A (p.Ser995=) | gnomAD v4 |
2 | g.135798114G>A | CA348591001 | LCT | c.4891C>T (p.Pro1631Ser) c.2984C>T (p.Ser995Phe) | |
2 | g.135798114G>C | CA348591002 | LCT | c.4891C>G (p.Pro1631Ala) c.2984C>G (p.Ser995Cys) | |
2 | g.135798114G>T | CA348591003 | LCT | c.4891C>A (p.Pro1631Thr) c.2984C>A (p.Ser995Tyr) | |
2 | g.135798115A>C | CA348591004 | LCT | c.4890T>G (p.His1630Gln) c.2983T>G (p.Ser995Ala) | |
2 | g.135798115A>G | CA429086226 | LCT | c.4890T>C (p.His1630=) c.2983T>C (p.Ser995Pro) | |
2 | g.135798115A>T | CA348591005 | LCT | c.4890T>A (p.His1630Gln) c.2983T>A (p.Ser995Thr) | |
2 | g.135798116T>A | CA348591006 | LCT | c.4889A>T (p.His1630Leu) c.2982A>T (p.Thr994=) | |
2 | g.135798116T>C | CA348591007 | LCT | c.4889A>G (p.His1630Arg) c.2982A>G (p.Thr994=) | |
2 | g.135798116T>G | CA348591008 | LCT | c.4889A>C (p.His1630Pro) c.2982A>C (p.Thr994=) | |
2 | g.135798117del | CA2661274469 | LCT | c.4888del (p.His1630IlefsTer12) c.2981del (p.Thr994AsnfsTer?) | gnomAD v4 |
2 | g.135798117G>A | CA348591009 | LCT | c.4888C>T (p.His1630Tyr) c.2981C>T (p.Thr994Ile) | dbSNP gnomAD v4 |
2 | g.135798117G>C | CA348591011 | LCT | c.4888C>G (p.His1630Asp) c.2981C>G (p.Thr994Arg) | gnomAD v4 |
2 | g.135798117G= | CA1290826534 | LCT | c.4888C= (p.His1630=) c.2981C= (p.Thr994=) | |
2 | g.135798117G>T | CA348591010 | LCT | c.4888C>A (p.His1630Asn) c.2981C>A (p.Thr994Lys) | gnomAD v4 |
2 | g.135798118T>A | CA429086230 | LCT | c.4887A>T (p.Ala1629=) c.2980A>T (p.Thr994Ser) | dbSNP gnomAD v2 gnomAD v4 |
2 | g.135798118T>C | CA429086231 | LCT | c.4887A>G (p.Ala1629=) c.2980A>G (p.Thr994Ala) | gnomAD v4 |
2 | g.135798118T>G | CA1887743 | LCT | c.4887A>C (p.Ala1629=) c.2980A>C (p.Thr994Pro) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.135798118T= | CA1290826535 | LCT | c.4887A= (p.Ala1629=) c.2980A= (p.Thr994=) | |
2 | g.135798119G>A | CA348591012 | LCT | c.4886C>T (p.Ala1629Val) c.2979C>T (p.Cys993=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135798119G>C | CA348591013 | LCT | c.4886C>G (p.Ala1629Gly) c.2979C>G (p.Cys993Trp) | |
2 | g.135798119G= | CA1290826536 | LCT | c.4886C= (p.Ala1629=) c.2979C= (p.Cys993=) | |
2 | g.135798119G>T | CA348591014 | LCT | c.4886C>A (p.Ala1629Glu) c.2979C>A (p.Cys993Ter) | gnomAD v4 |
2 | g.135798120del | CA2577107816 | LCT | c.4885del (p.Ala1629HisfsTer13) c.2978del (p.Cys993SerfsTer?) | |
2 | g.135798120C>A | CA348591015 | LCT | c.4885G>T (p.Ala1629Ser) c.2978G>T (p.Cys993Phe) | |
2 | g.135798120C>G | CA348591016 | LCT | c.4885G>C (p.Ala1629Pro) c.2978G>C (p.Cys993Ser) | |
2 | g.135798120C>T | CA348591017 | LCT | c.4885G>A (p.Ala1629Thr) c.2978G>A (p.Cys993Tyr) | gnomAD v4 |
2 | g.135798121A= | CA1290826537 | LCT | c.4884T= (p.Phe1628=) c.2977T= (p.Cys993=) | |
2 | g.135798121A>C | CA348591019 | LCT | c.4884T>G (p.Phe1628Leu) c.2977T>G (p.Cys993Gly) | |
2 | g.135798121A>G | CA56602756 | LCT | c.4884T>C (p.Phe1628=) c.2977T>C (p.Cys993Arg) | dbSNP |
2 | g.135798121A>T | CA348591018 | LCT | c.4884T>A (p.Phe1628Leu) c.2977T>A (p.Cys993Ser) | |
2 | g.135798122A>C | CA348591020 | LCT | c.4883T>G (p.Phe1628Cys) c.2976T>G (p.Val992=) | |
2 | g.135798122A>G | CA348591021 | LCT | c.4883T>C (p.Phe1628Ser) c.2976T>C (p.Val992=) | gnomAD v4 |
2 | g.135798122A>T | CA348591022 | LCT | c.4883T>A (p.Phe1628Tyr) c.2976T>A (p.Val992=) | |
2 | g.135798123A= | CA1290826538 | LCT | c.4882T= (p.Phe1628=) c.2975T= (p.Val992=) | |
2 | g.135798123A>C | CA348591023 | LCT | c.4882T>G (p.Phe1628Val) c.2975T>G (p.Val992Gly) | |
2 | g.135798123A>G | CA348591024 | LCT | c.4882T>C (p.Phe1628Leu) c.2975T>C (p.Val992Ala) | dbSNP |
2 | g.135798123A>T | CA348591025 | LCT | c.4882T>A (p.Phe1628Ile) c.2975T>A (p.Val992Asp) | |
2 | g.135798124C>A | CA348591026 | LCT | c.4881G>T (p.Trp1627Cys) c.2974G>T (p.Val992Phe) | COSMIC |
2 | g.135798124C>G | CA348591028 | LCT | c.4881G>C (p.Trp1627Cys) c.2974G>C (p.Val992Leu) | |
2 | g.135798124C>T | CA348591027 | LCT | c.4881G>A (p.Trp1627Ter) c.2974G>A (p.Val992Ile) | |
2 | g.135798125del | CA2577107817 | LCT | c.4881del (p.Trp1627CysfsTer15) c.2974del (p.Val992PhefsTer?) | gnomAD v4 |
2 | g.135798125C>A | CA348591029 | LCT | c.4880G>T (p.Trp1627Leu) c.2973G>T (p.Leu991=) | |
2 | g.135798125C>G | CA348591030 | LCT | c.4880G>C (p.Trp1627Ser) c.2973G>C (p.Leu991=) | |
2 | g.135798125C>T | CA348591031 | LCT | c.4880G>A (p.Trp1627Ter) c.2973G>A (p.Leu991=) | |
2 | g.135798126A>C | CA348591032 | LCT | c.4879T>G (p.Trp1627Gly) c.2972T>G (p.Leu991Arg) | |
2 | g.135798126A>G | CA348591033 | LCT | c.4879T>C (p.Trp1627Arg) c.2972T>C (p.Leu991Pro) | gnomAD v4 |
2 | g.135798126A>T | CA348591034 | LCT | c.4879T>A (p.Trp1627Arg) c.2972T>A (p.Leu991Gln) | |
2 | g.135798127G>A | CA429086235 | LCT | c.4878C>T (p.Gly1626=) c.2971C>T (p.Leu991=) | |
2 | g.135798127G>C | CA429086237 | LCT | c.4878C>G (p.Gly1626=) c.2971C>G (p.Leu991Val) | |
2 | g.135798127G>T | CA429086236 | LCT | c.4878C>A (p.Gly1626=) c.2971C>A (p.Leu991Met) | gnomAD v4 |
2 | g.135798128C>A | CA348591035 | LCT | c.4877G>T (p.Gly1626Val) c.2970G>T (p.Arg990Ser) | |
2 | g.135798128C>G | CA348591036 | LCT | c.4877G>C (p.Gly1626Ala) c.2970G>C (p.Arg990Ser) | |
2 | g.135798128C>T | CA348591037 | LCT | c.4877G>A (p.Gly1626Asp) c.2970G>A (p.Arg990=) | |
2 | g.135798129C>A | CA348591038 | LCT | c.4876G>T (p.Gly1626Cys) c.2969G>T (p.Arg990Met) | |
2 | g.135798129C>G | CA348591039 | LCT | c.4876G>C (p.Gly1626Arg) c.2969G>C (p.Arg990Thr) | |
2 | g.135798129C>T | CA348591040 | LCT | c.4876G>A (p.Gly1626Ser) c.2969G>A (p.Arg990Lys) | gnomAD v4 |
2 | g.135798130T>A | CA429086239 | LCT | c.4875A>T (p.Gly1625=) c.2968A>T (p.Arg990Trp) | |
2 | g.135798130T>C | CA56602763 | LCT | c.4875A>G (p.Gly1625=) c.2968A>G (p.Arg990Gly) | dbSNP gnomAD v4 |
2 | g.135798130T>G | CA429086242 | LCT | c.4875A>C (p.Gly1625=) c.2968A>C (p.Arg990=) | |
2 | g.135798130T= | CA1290826539 | LCT | c.4875A= (p.Gly1625=) c.2968A= (p.Arg990=) | |
2 | g.135798131C>A | CA348591041 | LCT | c.4874G>T (p.Gly1625Val) c.2967G>T (p.Gly989=) | |
2 | g.135798131C>G | CA348591043 | LCT | c.4874G>C (p.Gly1625Ala) c.2967G>C (p.Gly989=) | |
2 | g.135798131C>T | CA348591042 | LCT | c.4874G>A (p.Gly1625Glu) c.2967G>A (p.Gly989=) | COSMIC |
2 | g.135798132C>A | CA348591044 | LCT | c.4873G>T (p.Gly1625Ter) c.2966G>T (p.Gly989Val) | |
2 | g.135798132C>G | CA348591045 | LCT | c.4873G>C (p.Gly1625Arg) c.2966G>C (p.Gly989Ala) | |
2 | g.135798132C>T | CA348591046 | LCT | c.4873G>A (p.Gly1625Arg) c.2966G>A (p.Gly989Glu) | |
2 | g.135798133C>A | CA348591047 | LCT | c.4872G>T (p.Met1624Ile) c.2965G>T (p.Gly989Trp) | |
2 | g.135798133C>G | CA348591048 | LCT | c.4872G>C (p.Met1624Ile) c.2965G>C (p.Gly989Arg) | |
2 | g.135798133C>T | CA348591049 | LCT | c.4872G>A (p.Met1624Ile) c.2965G>A (p.Gly989Arg) | gnomAD v4 |
2 | g.135798134A= | CA1290826540 | LCT | c.4871T= (p.Met1624=) c.2964T= (p.His988=) | |
2 | g.135798134A>C | CA348591050 | LCT | c.4871T>G (p.Met1624Arg) c.2964T>G (p.His988Gln) | |
2 | g.135798134A>G | CA1887744 | LCT | c.4871T>C (p.Met1624Thr) c.2964T>C (p.His988=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.135798134A>T | CA348591051 | LCT | c.4871T>A (p.Met1624Lys) c.2964T>A (p.His988Gln) | |
2 | g.135798135T>A | CA348591052 | LCT | c.4870A>T (p.Met1624Leu) c.2963A>T (p.His988Leu) | |
2 | g.135798135T>C | CA348591053 | LCT | c.4870A>G (p.Met1624Val) c.2963A>G (p.His988Arg) | |
2 | g.135798135T>G | CA348591054 | LCT | c.4870A>C (p.Met1624Leu) c.2963A>C (p.His988Pro) | |
2 | g.135798136G>A | CA429086246 | LCT | c.4869C>T (p.Phe1623=) c.2962C>T (p.His988Tyr) | |
2 | g.135798136G>C | CA348591056 | LCT | c.4869C>G (p.Phe1623Leu) c.2962C>G (p.His988Asp) | |
2 | g.135798136G>T | CA348591055 | LCT | c.4869C>A (p.Phe1623Leu) c.2962C>A (p.His988Asn) | gnomAD v4 |
2 | g.135798137A>C | CA348591057 | LCT | c.4868T>G (p.Phe1623Cys) c.2961T>G (p.Val987=) | |
2 | g.135798137A>G | CA348591058 | LCT | c.4868T>C (p.Phe1623Ser) c.2961T>C (p.Val987=) | |
2 | g.135798137A>T | CA348591059 | LCT | c.4868T>A (p.Phe1623Tyr) c.2961T>A (p.Val987=) | |
2 | g.135798138A>C | CA348591060 | LCT | c.4867T>G (p.Phe1623Val) c.2960T>G (p.Val987Gly) | |
2 | g.135798138A>G | CA348591061 | LCT | c.4867T>C (p.Phe1623Leu) c.2960T>C (p.Val987Ala) | |
2 | g.135798138A>T | CA348591062 | LCT | c.4867T>A (p.Phe1623Ile) c.2960T>A (p.Val987Asp) | |
2 | g.135798139C>A | CA348591063 | LCT | c.4867-1G>T (n.4867-1G>T) c.2960-1G>T (n.2960-1G>T) | |
2 | g.135798139C>G | CA348591064 | LCT | c.4867-1G>C (n.4867-1G>C) c.2960-1G>C (n.2960-1G>C) | |
2 | g.135798139C>T | CA348591065 | LCT | c.4867-1G>A (n.4867-1G>A) c.2960-1G>A (n.2960-1G>A) | gnomAD v4 |
2 | g.135798140T>A | CA348591066 | LCT | c.4867-2A>T (n.4867-2A>T) c.2960-2A>T (n.2960-2A>T) | |
2 | g.135798140T>C | CA348591067 | LCT | c.4867-2A>G (n.4867-2A>G) c.2960-2A>G (n.2960-2A>G) | gnomAD v4 |
2 | g.135798140T>G | CA348591068 | LCT | c.4867-2A>C (n.4867-2A>C) c.2960-2A>C (n.2960-2A>C) | |
2 | g.135798141G>T | CA2661274493 | LCT | c.4867-3C>A (n.4867-3C>A) c.2960-3C>A (n.2960-3C>A) | gnomAD v4 |
2 | g.135798142C= | CA1290826541 | LCT | c.4867-4G= (n.4867-4G=) c.2960-4G= (n.2960-4G=) | |
2 | g.135798142C>T | CA1887745 | LCT | c.4867-4G>A (n.4867-4G>A) c.2960-4G>A (n.2960-4G>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135798143G>A | CA536394363 | LCT | c.4867-5C>T (n.4867-5C>T) c.2960-5C>T (n.2960-5C>T) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135798143G>C | CA2661274499 | LCT | c.4867-5C>G (n.4867-5C>G) c.2960-5C>G (n.2960-5C>G) | gnomAD v4 |
2 | g.135798143G= | CA1290826543 | LCT | c.4867-5C= (n.4867-5C=) c.2960-5C= (n.2960-5C=) | |
2 | g.135798143G>T | CA1290826542 | LCT | c.4867-5C>A (n.4867-5C>A) c.2960-5C>A (n.2960-5C>A) | ClinVar dbSNP gnomAD v4 |
2 | g.135798145del | CA2577107818 | LCT | c.4867-5del (n.4867-5del) c.2960-5del (n.2960-5del) | |
2 | g.135798144G>A | CA2661274503 | LCT | c.4867-6C>T (n.4867-6C>T) c.2960-6C>T (n.2960-6C>T) | gnomAD v4 |
2 | g.135798144G= | CA1290826544 | LCT | c.4867-6C= (n.4867-6C=) c.2960-6C= (n.2960-6C=) | |
2 | g.135798144G>T | CA56602775 | LCT | c.4867-6C>A (n.4867-6C>A) c.2960-6C>A (n.2960-6C>A) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135798145G>A | CA1290826546 | LCT | c.4867-7C>T (n.4867-7C>T) c.2960-7C>T (n.2960-7C>T) | dbSNP gnomAD v4 |
2 | g.135798145G= | CA1290826545 | LCT | c.4867-7C= (n.4867-7C=) c.2960-7C= (n.2960-7C=) | |
2 | g.135798145G>T | CA2661274506 | LCT | c.4867-7C>A (n.4867-7C>A) c.2960-7C>A (n.2960-7C>A) | gnomAD v4 |
2 | g.135798147A>G | CA2700693870 | LCT | c.4867-9T>C (n.4867-9T>C) c.2960-9T>C (n.2960-9T>C) | dbSNP |
2 | g.135798148G= | CA1290826547 | LCT | c.4867-10C= (n.4867-10C=) c.2960-10C= (n.2960-10C=) | |
2 | g.135798148G>T | CA1887746 | LCT | c.4867-10C>A (n.4867-10C>A) c.2960-10C>A (n.2960-10C>A) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135798149G>A | CA2661274508 | LCT | c.4867-11C>T (n.4867-11C>T) c.2960-11C>T (n.2960-11C>T) | gnomAD v4 |
2 | g.135798149G>T | CA2661274509 | LCT | c.4867-11C>A (n.4867-11C>A) c.2960-11C>A (n.2960-11C>A) | gnomAD v4 |
2 | g.135798150G>A | CA1290826549 | LCT | c.4867-12C>T (n.4867-12C>T) c.2960-12C>T (n.2960-12C>T) | dbSNP gnomAD v4 |
2 | g.135798150G>C | CA2661274513 | LCT | c.4867-12C>G (n.4867-12C>G) c.2960-12C>G (n.2960-12C>G) | gnomAD v4 |
2 | g.135798150G= | CA1290826548 | LCT | c.4867-12C= (n.4867-12C=) c.2960-12C= (n.2960-12C=) | |
2 | g.135798150G>T | CA2661274515 | LCT | c.4867-12C>A (n.4867-12C>A) c.2960-12C>A (n.2960-12C>A) | gnomAD v4 |
2 | g.135798151T>A | CA2661274517 | LCT | c.4867-13A>T (n.4867-13A>T) c.2960-13A>T (n.2960-13A>T) | gnomAD v4 |
2 | g.135798151T>G | CA2577107820 | LCT | c.4867-13A>C (n.4867-13A>C) c.2960-13A>C (n.2960-13A>C) | |
2 | g.135798152G>A | CA2661274518 | LCT | c.4867-14C>T (n.4867-14C>T) c.2960-14C>T (n.2960-14C>T) | gnomAD v4 |
2 | g.135798152G>C | CA1887747 | LCT | c.4867-14C>G (n.4867-14C>G) c.2960-14C>G (n.2960-14C>G) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.135798152G= | CA1290826550 | LCT | c.4867-14C= (n.4867-14C=) c.2960-14C= (n.2960-14C=) | |
2 | g.135798152G>T | CA1290826551 | LCT | c.4867-14C>A (n.4867-14C>A) c.2960-14C>A (n.2960-14C>A) | dbSNP gnomAD v4 |
2 | g.135798156del | CA2577107822 | LCT | c.4867-14del (n.4867-14del) c.2960-14del (n.2960-14del) | gnomAD v4 |
2 | g.135798153G>T | CA2661274521 | LCT | c.4867-15C>A (n.4867-15C>A) c.2960-15C>A (n.2960-15C>A) | gnomAD v4 |
2 | g.135798154G>A | CA536394543 | LCT | c.4867-16C>T (n.4867-16C>T) c.2960-16C>T (n.2960-16C>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135798154G= | CA1290826552 | LCT | c.4867-16C= (n.4867-16C=) c.2960-16C= (n.2960-16C=) | |
2 | g.135798154G>T | CA2661274523 | LCT | c.4867-16C>A (n.4867-16C>A) c.2960-16C>A (n.2960-16C>A) | gnomAD v4 |
2 | g.135798155G>A | CA1887748 | LCT | c.4867-17C>T (n.4867-17C>T) c.2960-17C>T (n.2960-17C>T) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135798155G= | CA1290826553 | LCT | c.4867-17C= (n.4867-17C=) c.2960-17C= (n.2960-17C=) | |
2 | g.135798155G>T | CA2661274528 | LCT | c.4867-17C>A (n.4867-17C>A) c.2960-17C>A (n.2960-17C>A) | gnomAD v4 |
2 | g.135798156G>A | CA2661274529 | LCT | c.4867-18C>T (n.4867-18C>T) c.2960-18C>T (n.2960-18C>T) | ClinVar gnomAD v4 |
2 | g.135798156G>T | CA2661274530 | LCT | c.4867-18C>A (n.4867-18C>A) c.2960-18C>A (n.2960-18C>A) | gnomAD v4 |
2 | g.135798158G>A | CA2661274531 | LCT | c.4867-20C>T (n.4867-20C>T) c.2960-20C>T (n.2960-20C>T) | gnomAD v4 |
2 | g.135798158G>T | CA2661274533 | LCT | c.4867-20C>A (n.4867-20C>A) c.2960-20C>A (n.2960-20C>A) | gnomAD v4 |
2 | g.135798159A= | CA1290826554 | LCT | c.4867-21T= (n.4867-21T=) c.2960-21T= (n.2960-21T=) | |
2 | g.135798159A>G | CA536394545 | LCT | c.4867-21T>C (n.4867-21T>C) c.2960-21T>C (n.2960-21T>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135798160C= | CA1290826555 | LCT | c.4867-22G= (n.4867-22G=) c.2960-22G= (n.2960-22G=) | |
2 | g.135798160C>G | CA2577107825 | LCT | c.4867-22G>C (n.4867-22G>C) c.2960-22G>C (n.2960-22G>C) | gnomAD v4 |
2 | g.135798160C>T | CA56602808 | LCT | c.4867-22G>A (n.4867-22G>A) c.2960-22G>A (n.2960-22G>A) | dbSNP gnomAD v4 |
2 | g.135798162G>A | CA2661274542 | LCT | c.4867-24C>T (n.4867-24C>T) c.2960-24C>T (n.2960-24C>T) | gnomAD v4 |
2 | g.135798162G>C | CA1290826557 | LCT | c.4867-24C>G (n.4867-24C>G) c.2960-24C>G (n.2960-24C>G) | dbSNP gnomAD v4 |
2 | g.135798162G= | CA1290826556 | LCT | c.4867-24C= (n.4867-24C=) c.2960-24C= (n.2960-24C=) | |
2 | g.135798162G>T | CA536394547 | LCT | c.4867-24C>A (n.4867-24C>A) c.2960-24C>A (n.2960-24C>A) | dbSNP gnomAD v2 gnomAD v4 |
2 | g.135798163C>T | CA2577107830 | LCT | c.4867-25G>A (n.4867-25G>A) c.2960-25G>A (n.2960-25G>A) | gnomAD v4 |
2 | g.135798165del | CA2661274544 | LCT | c.4867-25del (n.4867-25del) c.2960-25del (n.2960-25del) | gnomAD v4 |
2 | g.135798164C>A | CA2661274546 | LCT | c.4867-26G>T (n.4867-26G>T) c.2960-26G>T (n.2960-26G>T) | gnomAD v4 |
2 | g.135798164C>T | CA2661274547 | LCT | c.4867-26G>A (n.4867-26G>A) c.2960-26G>A (n.2960-26G>A) | gnomAD v4 |
2 | g.135798165C= | CA1290826558 | LCT | c.4867-27G= (n.4867-27G=) c.2960-27G= (n.2960-27G=) | |
2 | g.135798165C>T | CA1887749 | LCT | c.4867-27G>A (n.4867-27G>A) c.2960-27G>A (n.2960-27G>A) | dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.135798166A>G | CA2661274551 | LCT | c.4867-28T>C (n.4867-28T>C) c.2960-28T>C (n.2960-28T>C) | gnomAD v4 |
2 | g.135798166_135798167insCCTGTAACGCCTGGGCT | CA2661274555 | LCT | c.4867-29_4867-28insAGCCCAGGCGTTACAGG (n.4867-29_4867-28insAGCCCAGGCGTTACAGG) c.2960-29_2960-28insAGCCCAGGCGTTACAGG (n.2960-29_2960-28insAGCCCAGGCGTTACAGG) | gnomAD v4 |
2 | g.135798167G>A | CA1290826560 | LCT | c.4867-29C>T (n.4867-29C>T) c.2960-29C>T (n.2960-29C>T) | dbSNP |
2 | g.135798167G>C | CA2661274556 | LCT | c.4867-29C>G (n.4867-29C>G) c.2960-29C>G (n.2960-29C>G) | gnomAD v4 |
2 | g.135798167G= | CA1290826559 | LCT | c.4867-29C= (n.4867-29C=) c.2960-29C= (n.2960-29C=) | |
2 | g.135798168G>T | CA2577107833 | LCT | c.4867-30C>A (n.4867-30C>A) c.2960-30C>A (n.2960-30C>A) | gnomAD v4 |
2 | g.135798169C>A | CA2577107834 | LCT | c.4867-31G>T (n.4867-31G>T) c.2960-31G>T (n.2960-31G>T) | gnomAD v4 |
2 | g.135798169C= | CA1290826561 | LCT | c.4867-31G= (n.4867-31G=) c.2960-31G= (n.2960-31G=) | |
2 | g.135798169C>G | CA2752308374 | LCT | c.4867-31G>C (n.4867-31G>C) c.2960-31G>C (n.2960-31G>C) | |
2 | g.135798169C>T | CA1887750 | LCT | c.4867-31G>A (n.4867-31G>A) c.2960-31G>A (n.2960-31G>A) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135798170G>A | CA1887751 | LCT | c.4867-32C>T (n.4867-32C>T) c.2960-32C>T (n.2960-32C>T) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135798170G>C | CA2547246595 | LCT | c.4867-32C>G (n.4867-32C>G) c.2960-32C>G (n.2960-32C>G) | gnomAD v4 |
2 | g.135798170G= | CA1290826562 | LCT | c.4867-32C= (n.4867-32C=) c.2960-32C= (n.2960-32C=) | |
2 | g.135798170G>T | CA2577107836 | LCT | c.4867-32C>A (n.4867-32C>A) c.2960-32C>A (n.2960-32C>A) | gnomAD v4 |
2 | g.135798171T>G | CA2661274561 | LCT | c.4867-33A>C (n.4867-33A>C) c.2960-33A>C (n.2960-33A>C) | gnomAD v4 |
2 | g.135798173A= | CA1290826563 | LCT | c.4867-35T= (n.4867-35T=) c.2960-35T= (n.2960-35T=) | |
2 | g.135798173A>T | CA1887752 | LCT | c.4867-35T>A (n.4867-35T>A) c.2960-35T>A (n.2960-35T>A) | dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.135798177_135798186del | CA2661274562 | LCT | c.4867-44_4867-35del (n.4867-44_4867-35del) c.2960-44_2960-35del (n.2960-44_2960-35del) | gnomAD v4 |
2 | g.135798174C>T | CA2661274565 | LCT | c.4867-36G>A (n.4867-36G>A) c.2960-36G>A (n.2960-36G>A) | gnomAD v4 |
2 | g.135798175A>G | CA2661274567 | LCT | c.4867-37T>C (n.4867-37T>C) c.2960-37T>C (n.2960-37T>C) | gnomAD v4 |
2 | g.135798176G>A | CA2661274568 | LCT | c.4867-38C>T (n.4867-38C>T) c.2960-38C>T (n.2960-38C>T) | gnomAD v4 |
2 | g.135798176G>T | CA2661274569 | LCT | c.4867-38C>A (n.4867-38C>A) c.2960-38C>A (n.2960-38C>A) | gnomAD v4 |
2 | g.135798177G>C | CA1290826566 | LCT | c.4867-39C>G (n.4867-39C>G) c.2960-39C>G (n.2960-39C>G) | dbSNP |
2 | g.135798177G= | CA1290826564 | LCT | c.4867-39C= (n.4867-39C=) c.2960-39C= (n.2960-39C=) | |
2 | g.135798177G>T | CA1290826565 | LCT | c.4867-39C>A (n.4867-39C>A) c.2960-39C>A (n.2960-39C>A) | dbSNP gnomAD v4 |
2 | g.135798179G= | CA1290826567 | LCT | c.4867-41C= (n.4867-41C=) c.2960-41C= (n.2960-41C=) | |
2 | g.135798179G>T | CA1887753 | LCT | c.4867-41C>A (n.4867-41C>A) c.2960-41C>A (n.2960-41C>A) | dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.135798181dup | CA2661274573 | LCT | c.4867-41dup (n.4867-41dup) c.2960-41dup (n.2960-41dup) | gnomAD v4 |
2 | g.135798181del | CA2661274574 | LCT | c.4867-41del (n.4867-41del) c.2960-41del (n.2960-41del) | gnomAD v4 |
2 | g.135798180G>A | CA1887754 | LCT | c.4867-42C>T (n.4867-42C>T) c.2960-42C>T (n.2960-42C>T) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135798180G>C | CA2661274576 | LCT | c.4867-42C>G (n.4867-42C>G) c.2960-42C>G (n.2960-42C>G) | gnomAD v4 |
2 | g.135798180G= | CA1290826568 | LCT | c.4867-42C= (n.4867-42C=) c.2960-42C= (n.2960-42C=) | |
2 | g.135798180G>T | CA2577107837 | LCT | c.4867-42C>A (n.4867-42C>A) c.2960-42C>A (n.2960-42C>A) | gnomAD v4 |
2 | g.135798181G>A | CA2661274577 | LCT | c.4867-43C>T (n.4867-43C>T) c.2960-43C>T (n.2960-43C>T) | gnomAD v4 |
2 | g.135798181G>C | CA536394551 | LCT | c.4867-43C>G (n.4867-43C>G) c.2960-43C>G (n.2960-43C>G) | dbSNP gnomAD v2 gnomAD v4 |
2 | g.135798181G= | CA1290826569 | LCT | c.4867-43C= (n.4867-43C=) c.2960-43C= (n.2960-43C=) | |
2 | g.135798181G>T | CA1887755 | LCT | c.4867-43C>A (n.4867-43C>A) c.2960-43C>A (n.2960-43C>A) | dbSNP ExAC gnomAD v2 |
2 | g.135798182C>A | CA2661274579 | LCT | c.4867-44G>T (n.4867-44G>T) c.2960-44G>T (n.2960-44G>T) | gnomAD v4 |
2 | g.135798182C>T | CA2661274578 | LCT | c.4867-44G>A (n.4867-44G>A) c.2960-44G>A (n.2960-44G>A) | gnomAD v4 |
2 | g.135798183A= | CA1290826570 | LCT | c.4867-45T= (n.4867-45T=) c.2960-45T= (n.2960-45T=) | |
2 | g.135798183A>C | CA1887756 | LCT | c.4867-45T>G (n.4867-45T>G) c.2960-45T>G (n.2960-45T>G) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135798183A>T | CA2661274582 | LCT | c.4867-45T>A (n.4867-45T>A) c.2960-45T>A (n.2960-45T>A) | gnomAD v4 |
2 | g.135798184C>T | CA2661274584 | LCT | c.4867-46G>A (n.4867-46G>A) c.2960-46G>A (n.2960-46G>A) | gnomAD v4 |
2 | g.135798186G>A | CA2577107838 | LCT | c.4867-48C>T (n.4867-48C>T) c.2960-48C>T (n.2960-48C>T) | gnomAD v4 |
2 | g.135798186G>C | CA2752308375 | LCT | c.4867-48C>G (n.4867-48C>G) c.2960-48C>G (n.2960-48C>G) | |
2 | g.135798186G= | CA1290826571 | LCT | c.4867-48C= (n.4867-48C=) c.2960-48C= (n.2960-48C=) | |
2 | g.135798186G>T | CA536394553 | LCT | c.4867-48C>A (n.4867-48C>A) c.2960-48C>A (n.2960-48C>A) | dbSNP gnomAD v2 gnomAD v4 |
2 | g.135798187C>A | CA1290826573 | LCT | c.4867-49G>T (n.4867-49G>T) c.2960-49G>T (n.2960-49G>T) | dbSNP gnomAD v4 |
2 | g.135798187C= | CA1290826572 | LCT | c.4867-49G= (n.4867-49G=) c.2960-49G= (n.2960-49G=) | |
2 | g.135798189_135798190insAACACCAAACACACCC | CA2752308376 | LCT | c.4867-52_4867-51insGGGTGTGTTTGGTGTT (n.4867-52_4867-51insGGGTGTGTTTGGTGTT) c.2960-52_2960-51insGGGTGTGTTTGGTGTT (n.2960-52_2960-51insGGGTGTGTTTGGTGTT) | |
2 | g.135798190G>A | CA536394554 | LCT | c.4867-52C>T (n.4867-52C>T) c.2960-52C>T (n.2960-52C>T) | dbSNP gnomAD v2 gnomAD v4 |
2 | g.135798190G= | CA1290826574 | LCT | c.4867-52C= (n.4867-52C=) c.2960-52C= (n.2960-52C=) | |
2 | g.135798190G>T | CA2661274591 | LCT | c.4867-52C>A (n.4867-52C>A) c.2960-52C>A (n.2960-52C>A) | gnomAD v4 |
2 | g.135798192G>A | CA2661274592 | LCT | c.4867-54C>T (n.4867-54C>T) c.2960-54C>T (n.2960-54C>T) | gnomAD v4 |
2 | g.135798192G>C | CA2752308377 | LCT | c.4867-54C>G (n.4867-54C>G) c.2960-54C>G (n.2960-54C>G) | |
2 | g.135798193A= | CA1290826577 | LCT | c.4867-55T= (n.4867-55T=) c.2960-55T= (n.2960-55T=) | |
2 | g.135798193A>G | CA1290826576 | LCT | c.4867-55T>C (n.4867-55T>C) c.2960-55T>C (n.2960-55T>C) | dbSNP |
2 | g.135798193_135798196delinsACAG | CA1290826575 | LCT | c.4867-58_4867-55delinsCTGT (n.4867-58_4867-55delinsCTGT) c.2960-58_2960-55delinsCTGT (n.2960-58_2960-55delinsCTGT) | |
2 | g.135798196_135798198del | CA1290826578 | LCT | c.4867-58_4867-56del (n.4867-58_4867-56del) c.2960-58_2960-56del (n.2960-58_2960-56del) | dbSNP |
2 | g.135798196G>A | CA536394555 | LCT | c.4867-58C>T (n.4867-58C>T) c.2960-58C>T (n.2960-58C>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135798196G= | CA1290826579 | LCT | c.4867-58C= (n.4867-58C=) c.2960-58C= (n.2960-58C=) | |
2 | g.135798196G>T | CA2661274596 | LCT | c.4867-58C>A (n.4867-58C>A) c.2960-58C>A (n.2960-58C>A) | gnomAD v4 |
2 | g.135798197C>A | CA2661274600 | LCT | c.4867-59G>T (n.4867-59G>T) c.2960-59G>T (n.2960-59G>T) | gnomAD v4 |
2 | g.135798197C>T | CA2577107839 | LCT | c.4867-59G>A (n.4867-59G>A) c.2960-59G>A (n.2960-59G>A) | gnomAD v4 |
2 | g.135798200C>A | CA2577107840 | LCT | c.4867-62G>T (n.4867-62G>T) c.2960-62G>T (n.2960-62G>T) | |
2 | g.135798200C>T | CA2577107841 | LCT | c.4867-62G>A (n.4867-62G>A) c.2960-62G>A (n.2960-62G>A) | gnomAD v4 |
2 | g.135798201G>A | CA757423795 | LCT | c.4867-63C>T (n.4867-63C>T) c.2960-63C>T (n.2960-63C>T) | dbSNP gnomAD v3 gnomAD v4 |
2 | g.135798201G= | CA1290826580 | LCT | c.4867-63C= (n.4867-63C=) c.2960-63C= (n.2960-63C=) | |
2 | g.135798201G>T | CA2661274606 | LCT | c.4867-63C>A (n.4867-63C>A) c.2960-63C>A (n.2960-63C>A) | gnomAD v4 |
2 | g.135798202T>C | CA1290826582 | LCT | c.4867-64A>G (n.4867-64A>G) c.2960-64A>G (n.2960-64A>G) | dbSNP |
2 | g.135798202T= | CA1290826581 | LCT | c.4867-64A= (n.4867-64A=) c.2960-64A= (n.2960-64A=) | |
2 | g.135798202_135798203delinsTC | CA1290826583 | LCT | c.4867-65_4867-64delinsGA (n.4867-65_4867-64delinsGA) c.2960-65_2960-64delinsGA (n.2960-65_2960-64delinsGA) | |
2 | g.135798203C>A | CA1290826584 | LCT | c.4867-65G>T (n.4867-65G>T) c.2960-65G>T (n.2960-65G>T) | dbSNP gnomAD v4 |
2 | g.135798203C= | CA1290826585 | LCT | c.4867-65G= (n.4867-65G=) c.2960-65G= (n.2960-65G=) | |
2 | g.135798203C>T | CA56602853 | LCT | c.4867-65G>A (n.4867-65G>A) c.2960-65G>A (n.2960-65G>A) | dbSNP gnomAD v3 gnomAD v4 |
2 | g.135798206del | CA1036796369 | LCT | c.4867-65del (n.4867-65del) c.2960-65del (n.2960-65del) | dbSNP gnomAD v3 gnomAD v4 |
2 | g.135798205C>T | CA2661274611 | LCT | c.4867-67G>A (n.4867-67G>A) c.2960-67G>A (n.2960-67G>A) | gnomAD v4 |
2 | g.135798206C>A | CA757423800 | LCT | c.4867-68G>T (n.4867-68G>T) c.2960-68G>T (n.2960-68G>T) | dbSNP gnomAD v4 |
2 | g.135798206C= | CA1290826586 | LCT | c.4867-68G= (n.4867-68G=) c.2960-68G= (n.2960-68G=) | |
2 | g.135798206C>T | CA56602861 | LCT | c.4867-68G>A (n.4867-68G>A) c.2960-68G>A (n.2960-68G>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135798207G>A | CA56602862 | LCT | c.4867-69C>T (n.4867-69C>T) c.2960-69C>T (n.2960-69C>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135798207G= | CA1290826587 | LCT | c.4867-69C= (n.4867-69C=) c.2960-69C= (n.2960-69C=) | |
2 | g.135798207G>T | CA2661274613 | LCT | c.4867-69C>A (n.4867-69C>A) c.2960-69C>A (n.2960-69C>A) | gnomAD v4 |
2 | g.135798208C>A | CA2577107849 | LCT | c.4867-70G>T (n.4867-70G>T) c.2960-70G>T (n.2960-70G>T) | gnomAD v4 |