Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.135789641_135789652dup | CA2577107653 | LCT | c.5484_5495dup (p.Ala1832_Ser1833insLysPheTyrAla) | gnomAD v4 |
2 | g.135789652C>A | CA348586297 | LCT | c.5482G>T (p.Ala1828Ser) | |
2 | g.135789652C= | CA1290822682 | LCT | c.5482G= (p.Ala1828=) | |
2 | g.135789652C>G | CA348586300 | LCT | c.5482G>C (p.Ala1828Pro) | |
2 | g.135789652C>T | CA1887611 | LCT | c.5482G>A (p.Ala1828Thr) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135789653T>A | CA429085055 | LCT | c.5481A>T (p.Ser1827=) | |
2 | g.135789653T>C | CA429085056 | LCT | c.5481A>G (p.Ser1827=) | |
2 | g.135789653T>G | CA429085058 | LCT | c.5481A>C (p.Ser1827=) | |
2 | g.135789654G>A | CA348586306 | LCT | c.5480C>T (p.Ser1827Leu) | |
2 | g.135789654G>C | CA348586308 | LCT | c.5480C>G (p.Ser1827Ter) | |
2 | g.135789654G>T | CA348586310 | LCT | c.5480C>A (p.Ser1827Ter) | |
2 | g.135789655A>C | CA348586314 | LCT | c.5479T>G (p.Ser1827Ala) | |
2 | g.135789655A>G | CA348586317 | LCT | c.5479T>C (p.Ser1827Pro) | |
2 | g.135789655A>T | CA348586319 | LCT | c.5479T>A (p.Ser1827Thr) | |
2 | g.135789656T>A | CA429085059 | LCT | c.5478A>T (p.Ala1826=) | |
2 | g.135789656T>C | CA56595009 | LCT | c.5478A>G (p.Ala1826=) | dbSNP gnomAD v4 |
2 | g.135789656T>G | CA429085060 | LCT | c.5478A>C (p.Ala1826=) | |
2 | g.135789656T= | CA1290822683 | LCT | c.5478A= (p.Ala1826=) | |
2 | g.135789657G>A | CA348586321 | LCT | c.5477C>T (p.Ala1826Val) | |
2 | g.135789657G>C | CA348586324 | LCT | c.5477C>G (p.Ala1826Gly) | |
2 | g.135789657G>T | CA348586326 | LCT | c.5477C>A (p.Ala1826Glu) | |
2 | g.135789658del | CA2661273565 | LCT | c.5476del (p.Ala1826HisfsTer?) | gnomAD v4 |
2 | g.135789658C>A | CA348586336 | LCT | c.5476G>T (p.Ala1826Ser) | |
2 | g.135789658C>G | CA348586333 | LCT | c.5476G>C (p.Ala1826Pro) | |
2 | g.135789658C>T | CA348586331 | LCT | c.5476G>A (p.Ala1826Thr) | |
2 | g.135789659T>A | CA348586340 | LCT | c.5475A>T (p.Lys1825Asn) | |
2 | g.135789659T>C | CA429085061 | LCT | c.5475A>G (p.Lys1825=) | |
2 | g.135789659T>G | CA348586342 | LCT | c.5475A>C (p.Lys1825Asn) | |
2 | g.135789660T>A | CA348586344 | LCT | c.5474A>T (p.Lys1825Ile) | |
2 | g.135789660T>C | CA348586347 | LCT | c.5474A>G (p.Lys1825Arg) | |
2 | g.135789660T>G | CA348586349 | LCT | c.5474A>C (p.Lys1825Thr) | |
2 | g.135789661T>A | CA348586354 | LCT | c.5473A>T (p.Lys1825Ter) | |
2 | g.135789661T>C | CA348586356 | LCT | c.5473A>G (p.Lys1825Glu) | gnomAD v4 |
2 | g.135789661T>G | CA348586359 | LCT | c.5473A>C (p.Lys1825Gln) | |
2 | g.135789662G>A | CA429085064 | LCT | c.5472C>T (p.Pro1824=) | |
2 | g.135789662G>C | CA429085065 | LCT | c.5472C>G (p.Pro1824=) | |
2 | g.135789662G>T | CA429085066 | LCT | c.5472C>A (p.Pro1824=) | gnomAD v4 |
2 | g.135789663G>A | CA348586363 | LCT | c.5471C>T (p.Pro1824Leu) | |
2 | g.135789663G>C | CA348586365 | LCT | c.5471C>G (p.Pro1824Arg) | |
2 | g.135789663G>T | CA348586367 | LCT | c.5471C>A (p.Pro1824His) | |
2 | g.135789664G>A | CA348586370 | LCT | c.5470C>T (p.Pro1824Ser) | |
2 | g.135789664G>C | CA348586372 | LCT | c.5470C>G (p.Pro1824Ala) | |
2 | g.135789664G>T | CA348586374 | LCT | c.5470C>A (p.Pro1824Thr) | |
2 | g.135789665G>A | CA429085067 | LCT | c.5469C>T (p.Ile1823=) | gnomAD v4 |
2 | g.135789665G>C | CA348586377 | LCT | c.5469C>G (p.Ile1823Met) | |
2 | g.135789665G>T | CA429085068 | LCT | c.5469C>A (p.Ile1823=) | COSMIC |
2 | g.135789666A>C | CA348586380 | LCT | c.5468T>G (p.Ile1823Ser) | |
2 | g.135789666A>G | CA348586382 | LCT | c.5468T>C (p.Ile1823Thr) | |
2 | g.135789666A>T | CA348586386 | LCT | c.5468T>A (p.Ile1823Asn) | |
2 | g.135789667T>A | CA348586389 | LCT | c.5467A>T (p.Ile1823Phe) | |
2 | g.135789667T>C | CA348586392 | LCT | c.5467A>G (p.Ile1823Val) | dbSNP |
2 | g.135789667T>G | CA348586393 | LCT | c.5467A>C (p.Ile1823Leu) | |
2 | g.135789667T= | CA1290822684 | LCT | c.5467A= (p.Ile1823=) | |
2 | g.135789668C>A | CA348586397 | LCT | c.5466G>T (p.Arg1822Ser) | |
2 | g.135789668C= | CA1290822685 | LCT | c.5466G= (p.Arg1822=) | |
2 | g.135789668C>G | CA348586400 | LCT | c.5466G>C (p.Arg1822Ser) | |
2 | g.135789668C>T | CA56595012 | LCT | c.5466G>A (p.Arg1822=) | dbSNP |
2 | g.135789669C>A | CA348586404 | LCT | c.5465G>T (p.Arg1822Met) | |
2 | g.135789669C>G | CA348586407 | LCT | c.5465G>C (p.Arg1822Thr) | |
2 | g.135789669C>T | CA348586410 | LCT | c.5465G>A (p.Arg1822Lys) | |
2 | g.135789670T>A | CA348586412 | LCT | c.5464A>T (p.Arg1822Trp) | |
2 | g.135789670T>C | CA348586414 | LCT | c.5464A>G (p.Arg1822Gly) | COSMIC |
2 | g.135789670T>G | CA429085069 | LCT | c.5464A>C (p.Arg1822=) | |
2 | g.135789671T>A | CA429085070 | LCT | c.5463A>T (p.Pro1821=) | |
2 | g.135789671T>C | CA429085071 | LCT | c.5463A>G (p.Pro1821=) | |
2 | g.135789671T>G | CA429085072 | LCT | c.5463A>C (p.Pro1821=) | |
2 | g.135789672G>A | CA348586420 | LCT | c.5462C>T (p.Pro1821Leu) | |
2 | g.135789672G>C | CA348586423 | LCT | c.5462C>G (p.Pro1821Arg) | |
2 | g.135789672G>T | CA348586418 | LCT | c.5462C>A (p.Pro1821Gln) | |
2 | g.135789673G>A | CA348586426 | LCT | c.5461C>T (p.Pro1821Ser) | gnomAD v4 |
2 | g.135789673G>C | CA348586428 | LCT | c.5461C>G (p.Pro1821Ala) | |
2 | g.135789673G>T | CA348586427 | LCT | c.5461C>A (p.Pro1821Thr) | |
2 | g.135789674C>A | CA429085073 | LCT | c.5460G>T (p.Leu1820=) | |
2 | g.135789674C= | CA1290822686 | LCT | c.5460G= (p.Leu1820=) | |
2 | g.135789674C>G | CA429085074 | LCT | c.5460G>C (p.Leu1820=) | |
2 | g.135789674C>T | CA1887612 | LCT | c.5460G>A (p.Leu1820=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135789675A>C | CA348586430 | LCT | c.5459T>G (p.Leu1820Arg) | ClinVar |
2 | g.135789675A>G | CA348586429 | LCT | c.5459T>C (p.Leu1820Pro) | |
2 | g.135789675A>T | CA348586431 | LCT | c.5459T>A (p.Leu1820Gln) | |
2 | g.135789676G>A | CA429085075 | LCT | c.5458C>T (p.Leu1820=) | |
2 | g.135789676G>C | CA348586432 | LCT | c.5458C>G (p.Leu1820Val) | |
2 | g.135789676G>T | CA348586433 | LCT | c.5458C>A (p.Leu1820Met) | |
2 | g.135789677A>C | CA429085076 | LCT | c.5457T>G (p.Ser1819=) | |
2 | g.135789677A>G | CA429085077 | LCT | c.5457T>C (p.Ser1819=) | |
2 | g.135789677A>T | CA429085078 | LCT | c.5457T>A (p.Ser1819=) | |
2 | g.135789678G>A | CA348586434 | LCT | c.5456C>T (p.Ser1819Phe) | dbSNP gnomAD v2 gnomAD v4 |
2 | g.135789678G>C | CA348586435 | LCT | c.5456C>G (p.Ser1819Cys) | |
2 | g.135789678G= | CA1290822687 | LCT | c.5456C= (p.Ser1819=) | |
2 | g.135789678G>T | CA348586436 | LCT | c.5456C>A (p.Ser1819Tyr) | |
2 | g.135789679A>C | CA348586437 | LCT | c.5455T>G (p.Ser1819Ala) | |
2 | g.135789679A>G | CA348586438 | LCT | c.5455T>C (p.Ser1819Pro) | |
2 | g.135789679A>T | CA348586439 | LCT | c.5455T>A (p.Ser1819Thr) | |
2 | g.135789680A= | CA1290822688 | LCT | c.5454T= (p.Pro1818=) | |
2 | g.135789680A>C | CA429085079 | LCT | c.5454T>G (p.Pro1818=) | |
2 | g.135789680A>G | CA56595046 | LCT | c.5454T>C (p.Pro1818=) | dbSNP gnomAD v2 gnomAD v4 |
2 | g.135789680A>T | CA429085080 | LCT | c.5454T>A (p.Pro1818=) | |
2 | g.135789681G>A | CA348586440 | LCT | c.5453C>T (p.Pro1818Leu) | |
2 | g.135789681G>C | CA348586441 | LCT | c.5453C>G (p.Pro1818Arg) | COSMIC |
2 | g.135789681G>T | CA348586442 | LCT | c.5453C>A (p.Pro1818His) | dbSNP |
2 | g.135789682G>A | CA348586445 | LCT | c.5452C>T (p.Pro1818Ser) | dbSNP gnomAD v3 gnomAD v4 |
2 | g.135789682G>C | CA348586443 | LCT | c.5452C>G (p.Pro1818Ala) | |
2 | g.135789682G= | CA1290822689 | LCT | c.5452C= (p.Pro1818=) | |
2 | g.135789682G>T | CA348586444 | LCT | c.5452C>A (p.Pro1818Thr) | |
2 | g.135789683G>A | CA429085081 | LCT | c.5451C>T (p.Asp1817=) | |
2 | g.135789683G>C | CA348586446 | LCT | c.5451C>G (p.Asp1817Glu) | dbSNP |
2 | g.135789683G= | CA1290822690 | LCT | c.5451C= (p.Asp1817=) | |
2 | g.135789683G>T | CA348586447 | LCT | c.5451C>A (p.Asp1817Glu) | dbSNP |
2 | g.135789684T>A | CA348586448 | LCT | c.5450A>T (p.Asp1817Val) | |
2 | g.135789684T>C | CA348586449 | LCT | c.5450A>G (p.Asp1817Gly) | |
2 | g.135789684T>G | CA348586450 | LCT | c.5450A>C (p.Asp1817Ala) | |
2 | g.135789685C>A | CA348586451 | LCT | c.5449G>T (p.Asp1817Tyr) | |
2 | g.135789685C>G | CA348586452 | LCT | c.5449G>C (p.Asp1817His) | gnomAD v4 |
2 | g.135789685C>T | CA348586453 | LCT | c.5449G>A (p.Asp1817Asn) | |
2 | g.135789686A>C | CA348586454 | LCT | c.5448T>G (p.Ser1816Arg) | ClinVar dbSNP |
2 | g.135789686A>G | CA429085082 | LCT | c.5448T>C (p.Ser1816=) | |
2 | g.135789686A>T | CA348586455 | LCT | c.5448T>A (p.Ser1816Arg) | |
2 | g.135789687C>A | CA348586457 | LCT | c.5447G>T (p.Ser1816Ile) | |
2 | g.135789687C= | CA1290822691 | LCT | c.5447G= (p.Ser1816=) | |
2 | g.135789687C>G | CA1887613 | LCT | c.5447G>C (p.Ser1816Thr) | dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.135789687C>T | CA348586456 | LCT | c.5447G>A (p.Ser1816Asn) | gnomAD v4 |
2 | g.135789688T>A | CA348586458 | LCT | c.5446A>T (p.Ser1816Cys) | |
2 | g.135789688T>C | CA348586459 | LCT | c.5446A>G (p.Ser1816Gly) | gnomAD v4 |
2 | g.135789688T>G | CA348586460 | LCT | c.5446A>C (p.Ser1816Arg) | |
2 | g.135789689G>A | CA429085083 | LCT | c.5445C>T (p.Tyr1815=) | |
2 | g.135789689G>C | CA348586461 | LCT | c.5445C>G (p.Tyr1815Ter) | |
2 | g.135789689G>T | CA348586462 | LCT | c.5445C>A (p.Tyr1815Ter) | |
2 | g.135789690T>A | CA348586463 | LCT | c.5444A>T (p.Tyr1815Phe) | |
2 | g.135789690T>C | CA348586464 | LCT | c.5444A>G (p.Tyr1815Cys) | gnomAD v4 |
2 | g.135789690T>G | CA348586465 | LCT | c.5444A>C (p.Tyr1815Ser) | |
2 | g.135789691A>C | CA348586466 | LCT | c.5443T>G (p.Tyr1815Asp) | |
2 | g.135789691A>G | CA348586467 | LCT | c.5443T>C (p.Tyr1815His) | |
2 | g.135789691A>T | CA348586468 | LCT | c.5443T>A (p.Tyr1815Asn) | |
2 | g.135789692G>A | CA429085084 | LCT | c.5442C>T (p.Asn1814=) | |
2 | g.135789692G>C | CA348586469 | LCT | c.5442C>G (p.Asn1814Lys) | |
2 | g.135789692G>T | CA348586470 | LCT | c.5442C>A (p.Asn1814Lys) | |
2 | g.135789693T>A | CA348586471 | LCT | c.5441A>T (p.Asn1814Ile) | |
2 | g.135789693T>C | CA348586473 | LCT | c.5441A>G (p.Asn1814Ser) | |
2 | g.135789693T>G | CA348586472 | LCT | c.5441A>C (p.Asn1814Thr) | |
2 | g.135789694T>A | CA348586474 | LCT | c.5440A>T (p.Asn1814Tyr) | |
2 | g.135789694T>C | CA348586475 | LCT | c.5440A>G (p.Asn1814Asp) | gnomAD v4 |
2 | g.135789694T>G | CA348586476 | LCT | c.5440A>C (p.Asn1814His) | |
2 | g.135789695C>A | CA429085085 | LCT | c.5439G>T (p.Val1813=) | |
2 | g.135789695C= | CA1290822692 | LCT | c.5439G= (p.Val1813=) | |
2 | g.135789695C>G | CA429085087 | LCT | c.5439G>C (p.Val1813=) | dbSNP gnomAD v2 gnomAD v4 |
2 | g.135789695C>T | CA429085086 | LCT | c.5439G>A (p.Val1813=) | |
2 | g.135789696A>C | CA348586477 | LCT | c.5438T>G (p.Val1813Gly) | |
2 | g.135789696A>G | CA348586478 | LCT | c.5438T>C (p.Val1813Ala) | |
2 | g.135789696A>T | CA348586479 | LCT | c.5438T>A (p.Val1813Glu) | |
2 | g.135789697C>A | CA348586480 | LCT | c.5437G>T (p.Val1813Leu) | |
2 | g.135789697C>G | CA348586481 | LCT | c.5437G>C (p.Val1813Leu) | |
2 | g.135789697C>T | CA348586482 | LCT | c.5437G>A (p.Val1813Met) | |
2 | g.135789698A>C | CA348586483 | LCT | c.5436T>G (p.Phe1812Leu) | |
2 | g.135789698A>G | CA429085088 | LCT | c.5436T>C (p.Phe1812=) | gnomAD v4 |
2 | g.135789698A>T | CA348586484 | LCT | c.5436T>A (p.Phe1812Leu) | |
2 | g.135789699A>C | CA348586486 | LCT | c.5435T>G (p.Phe1812Cys) | |
2 | g.135789699A>G | CA348586489 | LCT | c.5435T>C (p.Phe1812Ser) | |
2 | g.135789699A>T | CA348586485 | LCT | c.5435T>A (p.Phe1812Tyr) | |
2 | g.135789700A= | CA1290822693 | LCT | c.5434T= (p.Phe1812=) | |
2 | g.135789700A>C | CA348586498 | LCT | c.5434T>G (p.Phe1812Val) | |
2 | g.135789700A>G | CA348586493 | LCT | c.5434T>C (p.Phe1812Leu) | dbSNP gnomAD v3 gnomAD v4 |
2 | g.135789700A>T | CA56595050 | LCT | c.5434T>A (p.Phe1812Ile) | dbSNP |
2 | g.135789701A= | CA1290822694 | LCT | c.5433T= (p.His1811=) | |
2 | g.135789701A>C | CA1887614 | LCT | c.5433T>G (p.His1811Gln) | dbSNP ExAC gnomAD v2 |
2 | g.135789701A>G | CA56595063 | LCT | c.5433T>C (p.His1811=) | dbSNP gnomAD v2 gnomAD v4 |
2 | g.135789701A>T | CA348586500 | LCT | c.5433T>A (p.His1811Gln) | |
2 | g.135789702T>A | CA348586502 | LCT | c.5432A>T (p.His1811Leu) | |
2 | g.135789702T>C | CA348586504 | LCT | c.5432A>G (p.His1811Arg) | gnomAD v4 |
2 | g.135789702T>G | CA348586505 | LCT | c.5432A>C (p.His1811Pro) | |
2 | g.135789703G>A | CA348586506 | LCT | c.5431C>T (p.His1811Tyr) | gnomAD v4 |
2 | g.135789703G>C | CA348586507 | LCT | c.5431C>G (p.His1811Asp) | |
2 | g.135789703G>T | CA348586509 | LCT | c.5431C>A (p.His1811Asn) | |
2 | g.135789704C>A | CA429085093 | LCT | c.5430G>T (p.Leu1810=) | |
2 | g.135789704C= | CA1290822695 | LCT | c.5430G= (p.Leu1810=) | |
2 | g.135789704C>G | CA429085092 | LCT | c.5430G>C (p.Leu1810=) | |
2 | g.135789704C>T | CA1887615 | LCT | c.5430G>A (p.Leu1810=) | dbSNP ExAC gnomAD v2 |
2 | g.135789705A>C | CA348586514 | LCT | c.5429T>G (p.Leu1810Arg) | |
2 | g.135789705A>G | CA348586512 | LCT | c.5429T>C (p.Leu1810Pro) | |
2 | g.135789705A>T | CA348586511 | LCT | c.5429T>A (p.Leu1810Gln) | |
2 | g.135789706G>A | CA429085094 | LCT | c.5428C>T (p.Leu1810=) | dbSNP |
2 | g.135789706G>C | CA348586518 | LCT | c.5428C>G (p.Leu1810Val) | |
2 | g.135789706G= | CA1290822696 | LCT | c.5428C= (p.Leu1810=) | |
2 | g.135789706G>T | CA348586519 | LCT | c.5428C>A (p.Leu1810Met) | |
2 | g.135789707A>C | CA429085095 | LCT | c.5427T>G (p.Gly1809=) | |
2 | g.135789707A>G | CA429085096 | LCT | c.5427T>C (p.Gly1809=) | |
2 | g.135789707A>T | CA429085097 | LCT | c.5427T>A (p.Gly1809=) | |
2 | g.135789708C>A | CA348586520 | LCT | c.5426G>T (p.Gly1809Val) | |
2 | g.135789708C>G | CA348586522 | LCT | c.5426G>C (p.Gly1809Ala) | |
2 | g.135789708C>T | CA348586525 | LCT | c.5426G>A (p.Gly1809Asp) | gnomAD v4 |
2 | g.135789709C>A | CA348586528 | LCT | c.5425G>T (p.Gly1809Cys) | |
2 | g.135789709C>G | CA348586529 | LCT | c.5425G>C (p.Gly1809Arg) | |
2 | g.135789709C>T | CA348586530 | LCT | c.5425G>A (p.Gly1809Ser) | gnomAD v4 |
2 | g.135789710A>C | CA348586533 | LCT | c.5424T>G (p.Phe1808Leu) | |
2 | g.135789710A>G | CA429085099 | LCT | c.5424T>C (p.Phe1808=) | |
2 | g.135789710A>T | CA348586535 | LCT | c.5424T>A (p.Phe1808Leu) | |
2 | g.135789711A>C | CA348586537 | LCT | c.5423T>G (p.Phe1808Cys) | COSMIC |
2 | g.135789711A>G | CA348586538 | LCT | c.5423T>C (p.Phe1808Ser) | |
2 | g.135789711A>T | CA348586539 | LCT | c.5423T>A (p.Phe1808Tyr) | |
2 | g.135789712A>C | CA348586552 | LCT | c.5422T>G (p.Phe1808Val) | |
2 | g.135789712A>G | CA348586555 | LCT | c.5422T>C (p.Phe1808Leu) | |
2 | g.135789712A>T | CA348586542 | LCT | c.5422T>A (p.Phe1808Ile) | |
2 | g.135789713T>A | CA348586556 | LCT | c.5421A>T (p.Arg1807Ser) | |
2 | g.135789713T>C | CA429085100 | LCT | c.5421A>G (p.Arg1807=) | |
2 | g.135789713T>G | CA348586557 | LCT | c.5421A>C (p.Arg1807Ser) | |
2 | g.135789714C>A | CA348586560 | LCT | c.5420G>T (p.Arg1807Ile) | gnomAD v4 |
2 | g.135789714C>G | CA348586564 | LCT | c.5420G>C (p.Arg1807Thr) | |
2 | g.135789714C>T | CA348586575 | LCT | c.5420G>A (p.Arg1807Lys) | gnomAD v4 |
2 | g.135789715T>A | CA348586580 | LCT | c.5419A>T (p.Arg1807Ter) | |
2 | g.135789715T>C | CA348586594 | LCT | c.5419A>G (p.Arg1807Gly) | |
2 | g.135789715T>G | CA429085102 | LCT | c.5419A>C (p.Arg1807=) | |
2 | g.135789716C>A | CA348586597 | LCT | c.5418G>T (p.Glu1806Asp) | |
2 | g.135789716C>G | CA348586600 | LCT | c.5418G>C (p.Glu1806Asp) | |
2 | g.135789716C>T | CA429085103 | LCT | c.5418G>A (p.Glu1806=) | COSMIC |
2 | g.135789717T>A | CA348586603 | LCT | c.5417A>T (p.Glu1806Val) | |
2 | g.135789717T>C | CA348586606 | LCT | c.5417A>G (p.Glu1806Gly) | gnomAD v4 |
2 | g.135789717T>G | CA348586611 | LCT | c.5417A>C (p.Glu1806Ala) | |
2 | g.135789718C>A | CA348586620 | LCT | c.5416G>T (p.Glu1806Ter) | |
2 | g.135789718C>G | CA348586625 | LCT | c.5416G>C (p.Glu1806Gln) | |
2 | g.135789718C>T | CA348586616 | LCT | c.5416G>A (p.Glu1806Lys) | |
2 | g.135789719T>A | CA429085105 | LCT | c.5415A>T (p.Ser1805=) | |
2 | g.135789719T>C | CA429085108 | LCT | c.5415A>G (p.Ser1805=) | dbSNP gnomAD v4 |
2 | g.135789719T>G | CA429085107 | LCT | c.5415A>C (p.Ser1805=) | |
2 | g.135789720G>A | CA348586629 | LCT | c.5414C>T (p.Ser1805Leu) | |
2 | g.135789720G>C | CA348586639 | LCT | c.5414C>G (p.Ser1805Ter) | |
2 | g.135789720G>T | CA348586641 | LCT | c.5414C>A (p.Ser1805Ter) | dbSNP |
2 | g.135789721A>C | CA348586646 | LCT | c.5413T>G (p.Ser1805Ala) | |
2 | g.135789721A>G | CA348586647 | LCT | c.5413T>C (p.Ser1805Pro) | |
2 | g.135789721A>T | CA348586651 | LCT | c.5413T>A (p.Ser1805Thr) | |
2 | g.135789724del | CA2661273566 | LCT | c.5413del (p.Ser1805GlnfsTer9) | gnomAD v4 |
2 | g.135789722A>C | CA348586654 | LCT | c.5412T>G (p.Phe1804Leu) | |
2 | g.135789722A>G | CA429085109 | LCT | c.5412T>C (p.Phe1804=) | |
2 | g.135789722A>T | CA348586653 | LCT | c.5412T>A (p.Phe1804Leu) | |
2 | g.135789723A>C | CA348586655 | LCT | c.5411T>G (p.Phe1804Cys) | |
2 | g.135789723A>G | CA348586657 | LCT | c.5411T>C (p.Phe1804Ser) | |
2 | g.135789723A>T | CA348586661 | LCT | c.5411T>A (p.Phe1804Tyr) | |
2 | g.135789724A>C | CA348586667 | LCT | c.5410T>G (p.Phe1804Val) | |
2 | g.135789724A>G | CA348586670 | LCT | c.5410T>C (p.Phe1804Leu) | |
2 | g.135789724A>T | CA348586673 | LCT | c.5410T>A (p.Phe1804Ile) | |
2 | g.135789725G>A | CA429085111 | LCT | c.5409C>T (p.Gly1803=) | |
2 | g.135789725G>C | CA429085112 | LCT | c.5409C>G (p.Gly1803=) | |
2 | g.135789725G>T | CA429085113 | LCT | c.5409C>A (p.Gly1803=) | gnomAD v4 |
2 | g.135789726C>A | CA348586688 | LCT | c.5408G>T (p.Gly1803Val) | |
2 | g.135789726C= | CA1290822697 | LCT | c.5408G= (p.Gly1803=) | |
2 | g.135789726C>G | CA1887616 | LCT | c.5408G>C (p.Gly1803Ala) | dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.135789726C>T | CA348586679 | LCT | c.5408G>A (p.Gly1803Asp) | |
2 | g.135789727C>A | CA348586691 | LCT | c.5407G>T (p.Gly1803Cys) | dbSNP gnomAD v4 |
2 | g.135789727C= | CA1290822698 | LCT | c.5407G= (p.Gly1803=) | |
2 | g.135789727C>G | CA348586697 | LCT | c.5407G>C (p.Gly1803Arg) | |
2 | g.135789727C>T | CA348586694 | LCT | c.5407G>A (p.Gly1803Ser) | |
2 | g.135789728T>A | CA429085119 | LCT | c.5406A>T (p.Thr1802=) | |
2 | g.135789728T>C | CA429085120 | LCT | c.5406A>G (p.Thr1802=) | dbSNP gnomAD v3 gnomAD v4 |
2 | g.135789728T>G | CA429085118 | LCT | c.5406A>C (p.Thr1802=) | |
2 | g.135789728T= | CA1290822699 | LCT | c.5406A= (p.Thr1802=) | |
2 | g.135789729G>A | CA348586700 | LCT | c.5405C>T (p.Thr1802Ile) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135789729G>C | CA348586702 | LCT | c.5405C>G (p.Thr1802Arg) | |
2 | g.135789729G= | CA1290822700 | LCT | c.5405C= (p.Thr1802=) | |
2 | g.135789729G>T | CA348586701 | LCT | c.5405C>A (p.Thr1802Lys) | |
2 | g.135789730T>A | CA348586704 | LCT | c.5404A>T (p.Thr1802Ser) | |
2 | g.135789730T>C | CA1887617 | LCT | c.5404A>G (p.Thr1802Ala) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135789730T>G | CA348586715 | LCT | c.5404A>C (p.Thr1802Pro) | |
2 | g.135789730T= | CA1290822701 | LCT | c.5404A= (p.Thr1802=) | |
2 | g.135789731G>A | CA429085121 | LCT | c.5403C>T (p.Ala1801=) | |
2 | g.135789731G>C | CA429085122 | LCT | c.5403C>G (p.Ala1801=) | |
2 | g.135789731G>T | CA429085124 | LCT | c.5403C>A (p.Ala1801=) | |
2 | g.135789732G>A | CA348586719 | LCT | c.5402C>T (p.Ala1801Val) | COSMIC |
2 | g.135789732G>C | CA348586722 | LCT | c.5402C>G (p.Ala1801Gly) | |
2 | g.135789732G>T | CA348586725 | LCT | c.5402C>A (p.Ala1801Asp) | |
2 | g.135789733C>A | CA348586728 | LCT | c.5401G>T (p.Ala1801Ser) | |
2 | g.135789733C>G | CA348586729 | LCT | c.5401G>C (p.Ala1801Pro) | |
2 | g.135789733C>T | CA348586730 | LCT | c.5401G>A (p.Ala1801Thr) | |
2 | g.135789734_135789737dup | CA2661273567 | LCT | c.5398_5401dup (p.Ala1801ValfsTer18) | gnomAD v4 |
2 | g.135789734C>A | CA348586731 | LCT | c.5400G>T (p.Trp1800Cys) | |
2 | g.135789734C>G | CA348586733 | LCT | c.5400G>C (p.Trp1800Cys) | |
2 | g.135789734C>T | CA348586735 | LCT | c.5400G>A (p.Trp1800Ter) | |
2 | g.135789735C>A | CA348586745 | LCT | c.5399G>T (p.Trp1800Leu) | |
2 | g.135789735C>G | CA348586738 | LCT | c.5399G>C (p.Trp1800Ser) | |
2 | g.135789735C>T | CA348586740 | LCT | c.5399G>A (p.Trp1800Ter) | gnomAD v4 |
2 | g.135789736A>C | CA348586748 | LCT | c.5398T>G (p.Trp1800Gly) | |
2 | g.135789736A>G | CA348586752 | LCT | c.5398T>C (p.Trp1800Arg) | gnomAD v4 |
2 | g.135789736A>T | CA348586754 | LCT | c.5398T>A (p.Trp1800Arg) | |
2 | g.135789737C>A | CA348586761 | LCT | c.5397G>T (p.Glu1799Asp) | |
2 | g.135789737C>G | CA348586763 | LCT | c.5397G>C (p.Glu1799Asp) | |
2 | g.135789737C>T | CA429085129 | LCT | c.5397G>A (p.Glu1799=) | |
2 | g.135789738T>A | CA348586768 | LCT | c.5396A>T (p.Glu1799Val) | COSMIC |
2 | g.135789738T>C | CA348586772 | LCT | c.5396A>G (p.Glu1799Gly) | |
2 | g.135789738T>G | CA348586775 | LCT | c.5396A>C (p.Glu1799Ala) | |
2 | g.135789739C>A | CA348586779 | LCT | c.5395G>T (p.Glu1799Ter) | |
2 | g.135789739C= | CA1290822702 | LCT | c.5395G= (p.Glu1799=) | |
2 | g.135789739C>G | CA348586783 | LCT | c.5395G>C (p.Glu1799Gln) | gnomAD v4 |
2 | g.135789739C>T | CA56595076 | LCT | c.5395G>A (p.Glu1799Lys) | dbSNP gnomAD v3 gnomAD v4 |
2 | g.135789740A= | CA1290822703 | LCT | c.5394T= (p.Phe1798=) | |
2 | g.135789740A>C | CA348586792 | LCT | c.5394T>G (p.Phe1798Leu) | |
2 | g.135789740A>G | CA429085131 | LCT | c.5394T>C (p.Phe1798=) | dbSNP gnomAD v3 gnomAD v4 |
2 | g.135789740A>T | CA348586796 | LCT | c.5394T>A (p.Phe1798Leu) | |
2 | g.135789741A= | CA1290822704 | LCT | c.5393T= (p.Phe1798=) | |
2 | g.135789741A>C | CA348586801 | LCT | c.5393T>G (p.Phe1798Cys) | |
2 | g.135789741A>G | CA1887618 | LCT | c.5393T>C (p.Phe1798Ser) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135789741A>T | CA348586806 | LCT | c.5393T>A (p.Phe1798Tyr) | dbSNP |
2 | g.135789742A>C | CA348586817 | LCT | c.5392T>G (p.Phe1798Val) | |
2 | g.135789742A>G | CA348586819 | LCT | c.5392T>C (p.Phe1798Leu) | |
2 | g.135789742A>T | CA348586822 | LCT | c.5392T>A (p.Phe1798Ile) | |
2 | g.135789743A= | CA1290822705 | LCT | c.5391T= (p.Asn1797=) | |
2 | g.135789743A>C | CA348586830 | LCT | c.5391T>G (p.Asn1797Lys) | |
2 | g.135789743A>G | CA1887619 | LCT | c.5391T>C (p.Asn1797=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135789743A>T | CA348586835 | LCT | c.5391T>A (p.Asn1797Lys) | |
2 | g.135789744T>A | CA348586839 | LCT | c.5390A>T (p.Asn1797Ile) | |
2 | g.135789744T>C | CA348586844 | LCT | c.5390A>G (p.Asn1797Ser) | |
2 | g.135789744T>G | CA348586846 | LCT | c.5390A>C (p.Asn1797Thr) | |
2 | g.135789745T>A | CA348586855 | LCT | c.5389A>T (p.Asn1797Tyr) | |
2 | g.135789745T>C | CA348586854 | LCT | c.5389A>G (p.Asn1797Asp) | gnomAD v4 |
2 | g.135789745T>G | CA348586851 | LCT | c.5389A>C (p.Asn1797His) | |
2 | g.135789746G>A | CA429085133 | LCT | c.5388C>T (p.Asp1796=) | |
2 | g.135789746G>C | CA348586856 | LCT | c.5388C>G (p.Asp1796Glu) | |
2 | g.135789746G>T | CA348586858 | LCT | c.5388C>A (p.Asp1796Glu) | |
2 | g.135789746_135789747delinsGT | CA1290822706 | LCT | c.5387_5388delinsAC (p.Asp1796=) | |
2 | g.135789747del | CA144322 | LCT | c.5387del (p.Asp1796AlafsTer18) | ClinVar dbSNP |
2 | g.135789747T>A | CA348586864 | LCT | c.5387A>T (p.Asp1796Val) | |
2 | g.135789747T>C | CA348586867 | LCT | c.5387A>G (p.Asp1796Gly) | |
2 | g.135789747T>G | CA348586877 | LCT | c.5387A>C (p.Asp1796Ala) | |
2 | g.135789748C>A | CA348586883 | LCT | c.5386G>T (p.Asp1796Tyr) | |
2 | g.135789748C>G | CA348586884 | LCT | c.5386G>C (p.Asp1796His) | |
2 | g.135789748C>T | CA348586886 | LCT | c.5386G>A (p.Asp1796Asn) | |
2 | g.135789749del | CA2661273568 | LCT | c.5386del (p.Asp1796ThrfsTer18) | gnomAD v4 |
2 | g.135789749C>A | CA348586889 | LCT | c.5385G>T (p.Met1795Ile) | |
2 | g.135789749C>G | CA348586890 | LCT | c.5385G>C (p.Met1795Ile) | |
2 | g.135789749C>T | CA348586891 | LCT | c.5385G>A (p.Met1795Ile) | |
2 | g.135789750A= | CA1290822707 | LCT | c.5384T= (p.Met1795=) | |
2 | g.135789750A>C | CA348586901 | LCT | c.5384T>G (p.Met1795Arg) | |
2 | g.135789750A>G | CA348586898 | LCT | c.5384T>C (p.Met1795Thr) | dbSNP gnomAD v3 gnomAD v4 |
2 | g.135789750A>T | CA348586894 | LCT | c.5384T>A (p.Met1795Lys) | dbSNP gnomAD v2 gnomAD v4 |
2 | g.135789751T>A | CA348586904 | LCT | c.5383A>T (p.Met1795Leu) | |
2 | g.135789751T>C | CA348586906 | LCT | c.5383A>G (p.Met1795Val) | dbSNP gnomAD v4 |
2 | g.135789751T>G | CA348586905 | LCT | c.5383A>C (p.Met1795Leu) | |
2 | g.135789751T= | CA1290822708 | LCT | c.5383A= (p.Met1795=) | |
2 | g.135789752C>A | CA429085135 | LCT | c.5382G>T (p.Ala1794=) | |
2 | g.135789752C= | CA1290822709 | LCT | c.5382G= (p.Ala1794=) | |
2 | g.135789752C>G | CA429085136 | LCT | c.5382G>C (p.Ala1794=) | |
2 | g.135789752C>T | CA429085137 | LCT | c.5382G>A (p.Ala1794=) | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC |