14 | g.49621876A>C | CA389619531 | MGAT2 | c.608A>C (p.Asn203Thr)
| |
14 | g.49621876A>G | CA389619532 | MGAT2 | c.608A>G (p.Asn203Ser)
| |
14 | g.49621876A>T | CA389619533 | MGAT2 | c.608A>T (p.Asn203Ile)
| |
14 | g.49621877T>A | CA389619535 | MGAT2 | c.609T>A (p.Asn203Lys)
| |
14 | g.49621877T>C | CA7172582 | MGAT2 | c.609T>C (p.Asn203=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.49621877T>G | CA389619537 | MGAT2 | c.609T>G (p.Asn203Lys)
| |
14 | g.49621877T= | CA2135804723 | MGAT2 | c.609T= (p.Asn203=)
| |
14 | g.49621878G>A | CA389619539 | MGAT2 | c.610G>A (p.Ala204Thr)
| |
14 | g.49621878G>C | CA389619540 | MGAT2 | c.610G>C (p.Ala204Pro)
| |
14 | g.49621878G>T | CA389619542 | MGAT2 | c.610G>T (p.Ala204Ser)
| |
14 | g.49621879C>A | CA389619543 | MGAT2 | c.611C>A (p.Ala204Asp)
| |
14 | g.49621879C= | CA2135804724 | MGAT2 | c.611C= (p.Ala204=)
| |
14 | g.49621879C>G | CA389619545 | MGAT2 | c.611C>G (p.Ala204Gly)
| gnomAD v4 |
14 | g.49621879C>T | CA389619547 | MGAT2 | c.611C>T (p.Ala204Val)
| dbSNP gnomAD v2 gnomAD v4 |
14 | g.49621880C>A | CA486350331 | MGAT2 | c.612C>A (p.Ala204=)
| COSMIC |
14 | g.49621880C= | CA2135804725 | MGAT2 | c.612C= (p.Ala204=)
| |
14 | g.49621880C>G | CA486350332 | MGAT2 | c.612C>G (p.Ala204=)
| |
14 | g.49621880C>T | CA260660733 | MGAT2 | c.612C>T (p.Ala204=)
| dbSNP gnomAD v4 |
14 | g.49621881G>A | CA389619552 | MGAT2 | c.613G>A (p.Ala205Thr)
| gnomAD v4 |
14 | g.49621881G>C | CA389619550 | MGAT2 | c.613G>C (p.Ala205Pro)
| gnomAD v4 |
14 | g.49621881G>T | CA389619548 | MGAT2 | c.613G>T (p.Ala205Ser)
| |
14 | g.49621882C>A | CA389619554 | MGAT2 | c.614C>A (p.Ala205Asp)
| |
14 | g.49621882C>G | CA389619556 | MGAT2 | c.614C>G (p.Ala205Gly)
| |
14 | g.49621882C>T | CA389619557 | MGAT2 | c.614C>T (p.Ala205Val)
| |
14 | g.49621883T>A | CA486350336 | MGAT2 | c.615T>A (p.Ala205=)
| |
14 | g.49621883T>C | CA486350338 | MGAT2 | c.615T>C (p.Ala205=)
| gnomAD v4 |
14 | g.49621883T>G | CA486350339 | MGAT2 | c.615T>G (p.Ala205=)
| |
14 | g.49621884T>A | CA389619559 | MGAT2 | c.616T>A (p.Leu206Met)
| |
14 | g.49621884T>C | CA486350340 | MGAT2 | c.616T>C (p.Leu206=)
| dbSNP |
14 | g.49621884T>G | CA260660736 | MGAT2 | c.616T>G (p.Leu206Val)
| dbSNP gnomAD v4 |
14 | g.49621884T= | CA2135804726 | MGAT2 | c.616T= (p.Leu206=)
| |
14 | g.49621885T>A | CA389619561 | MGAT2 | c.617T>A (p.Leu206Ter)
| |
14 | g.49621885T>C | CA389619562 | MGAT2 | c.617T>C (p.Leu206Ser)
| |
14 | g.49621885T>G | CA389619564 | MGAT2 | c.617T>G (p.Leu206Trp)
| |
14 | g.49621886G>A | CA486350344 | MGAT2 | c.618G>A (p.Leu206=)
| COSMIC |
14 | g.49621886G>C | CA389619565 | MGAT2 | c.618G>C (p.Leu206Phe)
| |
14 | g.49621886G>T | CA389619567 | MGAT2 | c.618G>T (p.Leu206Phe)
| |
14 | g.49621887A>C | CA389619568 | MGAT2 | c.619A>C (p.Lys207Gln)
| |
14 | g.49621887A>G | CA389619569 | MGAT2 | c.619A>G (p.Lys207Glu)
| |
14 | g.49621887A>T | CA389619570 | MGAT2 | c.619A>T (p.Lys207Ter)
| |
14 | g.49621888A>C | CA389619574 | MGAT2 | c.620A>C (p.Lys207Thr)
| |
14 | g.49621888A>G | CA389619571 | MGAT2 | c.620A>G (p.Lys207Arg)
| |
14 | g.49621888A>T | CA389619572 | MGAT2 | c.620A>T (p.Lys207Ile)
| |
14 | g.49621889A= | CA2135804727 | MGAT2 | c.621A= (p.Lys207=)
| |
14 | g.49621889A>C | CA389619575 | MGAT2 | c.621A>C (p.Lys207Asn)
| |
14 | g.49621889A>G | CA486350345 | MGAT2 | c.621A>G (p.Lys207=)
| dbSNP |
14 | g.49621889A>T | CA389619577 | MGAT2 | c.621A>T (p.Lys207Asn)
| |
14 | g.49621890T>A | CA389619578 | MGAT2 | c.622T>A (p.Leu208Met)
| |
14 | g.49621890T>C | CA7172583 | MGAT2 | c.622T>C (p.Leu208=)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
14 | g.49621890T>G | CA389619581 | MGAT2 | c.622T>G (p.Leu208Val)
| |
14 | g.49621890T= | CA2135804728 | MGAT2 | c.622T= (p.Leu208=)
| |
14 | g.49621891T>A | CA389619582 | MGAT2 | c.623T>A (p.Leu208Ter)
| |
14 | g.49621891T>C | CA389619584 | MGAT2 | c.623T>C (p.Leu208Ser)
| |
14 | g.49621891T>G | CA389619585 | MGAT2 | c.623T>G (p.Leu208Trp)
| |
14 | g.49621891_49621893delinsTGG | CA2135804729 | MGAT2 | c.623_625delinsTGG (p.Leu208=)
| |
14 | g.49621892G>A | CA486350348 | MGAT2 | c.624G>A (p.Leu208=)
| |
14 | g.49621892G>C | CA389619586 | MGAT2 | c.624G>C (p.Leu208Phe)
| |
14 | g.49621892G>T | CA389619588 | MGAT2 | c.624G>T (p.Leu208Phe)
| |
14 | g.49621894_49621895del | CA706480752 | MGAT2 | c.626_627del (p.Gly209ValfsTer5)
| dbSNP gnomAD v3 gnomAD v4 |
14 | g.49621893G>A | CA389619589 | MGAT2 | c.625G>A (p.Gly209Arg)
| gnomAD v4 |
14 | g.49621893G>C | CA389619591 | MGAT2 | c.625G>C (p.Gly209Arg)
| |
14 | g.49621893G= | CA2135804730 | MGAT2 | c.625G= (p.Gly209=)
| |
14 | g.49621893G>T | CA389619593 | MGAT2 | c.625G>T (p.Gly209Trp)
| dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.49621894G>A | CA389619597 | MGAT2 | c.626G>A (p.Gly209Glu)
| |
14 | g.49621894G>C | CA389619596 | MGAT2 | c.626G>C (p.Gly209Ala)
| |
14 | g.49621894G>T | CA389619594 | MGAT2 | c.626G>T (p.Gly209Val)
| gnomAD v4 |
14 | g.49621895G>A | CA486350354 | MGAT2 | c.627G>A (p.Gly209=)
| gnomAD v4 |
14 | g.49621895G>C | CA486350355 | MGAT2 | c.627G>C (p.Gly209=)
| |
14 | g.49621895G>T | CA486350353 | MGAT2 | c.627G>T (p.Gly209=)
| |
14 | g.49621896T>A | CA389619599 | MGAT2 | c.628T>A (p.Cys210Ser)
| |
14 | g.49621896T>C | CA389619600 | MGAT2 | c.628T>C (p.Cys210Arg)
| |
14 | g.49621896T>G | CA389619601 | MGAT2 | c.628T>G (p.Cys210Gly)
| |
14 | g.49621897G>A | CA389619603 | MGAT2 | c.629G>A (p.Cys210Tyr)
| |
14 | g.49621897G>C | CA389619605 | MGAT2 | c.629G>C (p.Cys210Ser)
| gnomAD v4 |
14 | g.49621897G>T | CA389619606 | MGAT2 | c.629G>T (p.Cys210Phe)
| |
14 | g.49621898C>A | CA389619609 | MGAT2 | c.630C>A (p.Cys210Ter)
| |
14 | g.49621898C= | CA2135804731 | MGAT2 | c.630C= (p.Cys210=)
| |
14 | g.49621898C>G | CA389619612 | MGAT2 | c.630C>G (p.Cys210Trp)
| |
14 | g.49621898C>T | CA486350358 | MGAT2 | c.630C>T (p.Cys210=)
| dbSNP gnomAD v2 gnomAD v4 |
14 | g.49621899A= | CA2135804732 | MGAT2 | c.631A= (p.Ile211=)
| |
14 | g.49621899A>C | CA389619613 | MGAT2 | c.631A>C (p.Ile211Leu)
| |
14 | g.49621899A>G | CA389619617 | MGAT2 | c.631A>G (p.Ile211Val)
| dbSNP gnomAD v3 gnomAD v4 |
14 | g.49621899A>T | CA389619616 | MGAT2 | c.631A>T (p.Ile211Phe)
| |
14 | g.49621900T>A | CA389619619 | MGAT2 | c.632T>A (p.Ile211Asn)
| |
14 | g.49621900T>C | CA389619620 | MGAT2 | c.632T>C (p.Ile211Thr)
| |
14 | g.49621900T>G | CA389619622 | MGAT2 | c.632T>G (p.Ile211Ser)
| |
14 | g.49621901C>A | CA486350361 | MGAT2 | c.633C>A (p.Ile211=)
| |
14 | g.49621901C>G | CA389619625 | MGAT2 | c.633C>G (p.Ile211Met)
| gnomAD v4 |
14 | g.49621901C>T | CA486350360 | MGAT2 | c.633C>T (p.Ile211=)
| gnomAD v4 COSMIC |
14 | g.49621902A>C | CA389619626 | MGAT2 | c.634A>C (p.Asn212His)
| |
14 | g.49621902A>G | CA389619632 | MGAT2 | c.634A>G (p.Asn212Asp)
| |
14 | g.49621902A>T | CA389619629 | MGAT2 | c.634A>T (p.Asn212Tyr)
| |
14 | g.49621902_49621903insC | CA2570222421 | MGAT2 | c.634_635insC (p.Asn212ThrfsTer3)
| |
14 | g.49621903A= | CA2135804733 | MGAT2 | c.635A= (p.Asn212=)
| |
14 | g.49621903A>C | CA389619634 | MGAT2 | c.635A>C (p.Asn212Thr)
| |
14 | g.49621903A>G | CA7172584 | MGAT2 | c.635A>G (p.Asn212Ser)
| dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
14 | g.49621903A>T | CA389619636 | MGAT2 | c.635A>T (p.Asn212Ile)
| gnomAD v4 |
14 | g.49621903_49621904insATGAAATGCCTGAACTGGCAGTAGTTTCTGATGATACCTTGATTGAAAAAGTAGTCAAAGCCCAAGATGACCGTCTCTTCTACGTATCAGAAGCTATTCGCCGTGGCTACACACCAGAAGAAAT | CA2563482155 | MGAT2 | c.635_636insATGAAATGCCTGAACTGGCAGTAGTTTCTGATGATACCTTGATTGAAAAAGTAGTCAAAGCCCAAGATGACCGTCTCTTCTACGTATCAGAAGCTATTCGCCGTGGCTACACACCAGAAGAAAT (p.Asn212LysfsTer2)
| |
14 | g.49621904T>A | CA389619639 | MGAT2 | c.636T>A (p.Asn212Lys)
| gnomAD v4 |
14 | g.49621904T>C | CA7172585 | MGAT2 | c.636T>C (p.Asn212=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.49621904T>G | CA389619643 | MGAT2 | c.636T>G (p.Asn212Lys)
| |
14 | g.49621904T= | CA2135804734 | MGAT2 | c.636T= (p.Asn212=)
| |
14 | g.49621905G>A | CA389619645 | MGAT2 | c.637G>A (p.Ala213Thr)
| |
14 | g.49621905G>C | CA389619648 | MGAT2 | c.637G>C (p.Ala213Pro)
| |
14 | g.49621905G>T | CA389619651 | MGAT2 | c.637G>T (p.Ala213Ser)
| |
14 | g.49621906C>A | CA389619652 | MGAT2 | c.638C>A (p.Ala213Asp)
| |
14 | g.49621906C= | CA2135804735 | MGAT2 | c.638C= (p.Ala213=)
| |
14 | g.49621906C>G | CA389619653 | MGAT2 | c.638C>G (p.Ala213Gly)
| dbSNP |
14 | g.49621906C>T | CA389619656 | MGAT2 | c.638C>T (p.Ala213Val)
| |
14 | g.49621907T>A | CA486350364 | MGAT2 | c.639T>A (p.Ala213=)
| gnomAD v4 |
14 | g.49621907T>C | CA486350366 | MGAT2 | c.639T>C (p.Ala213=)
| |
14 | g.49621907T>G | CA486350368 | MGAT2 | c.639T>G (p.Ala213=)
| |
14 | g.49621908G>A | CA389619662 | MGAT2 | c.640G>A (p.Glu214Lys)
| |
14 | g.49621908G>C | CA389619658 | MGAT2 | c.640G>C (p.Glu214Gln)
| |
14 | g.49621908G>T | CA389619661 | MGAT2 | c.640G>T (p.Glu214Ter)
| COSMIC |
14 | g.49621909A>C | CA389619664 | MGAT2 | c.641A>C (p.Glu214Ala)
| |
14 | g.49621909A>G | CA389619667 | MGAT2 | c.641A>G (p.Glu214Gly)
| |
14 | g.49621909A>T | CA389619670 | MGAT2 | c.641A>T (p.Glu214Val)
| |
14 | g.49621910G>A | CA486350370 | MGAT2 | c.642G>A (p.Glu214=)
| |
14 | g.49621910G>C | CA389619672 | MGAT2 | c.642G>C (p.Glu214Asp)
| |
14 | g.49621910G>T | CA389619673 | MGAT2 | c.642G>T (p.Glu214Asp)
| |
14 | g.49621911T>A | CA389619675 | MGAT2 | c.643T>A (p.Tyr215Asn)
| |
14 | g.49621911T>C | CA389619677 | MGAT2 | c.643T>C (p.Tyr215His)
| |
14 | g.49621911T>G | CA389619678 | MGAT2 | c.643T>G (p.Tyr215Asp)
| |
14 | g.49621912A>C | CA389619680 | MGAT2 | c.644A>C (p.Tyr215Ser)
| |
14 | g.49621912A>G | CA389619682 | MGAT2 | c.644A>G (p.Tyr215Cys)
| |
14 | g.49621912A>T | CA389619685 | MGAT2 | c.644A>T (p.Tyr215Phe)
| |
14 | g.49621913T>A | CA389619688 | MGAT2 | c.645T>A (p.Tyr215Ter)
| |
14 | g.49621913T>C | CA486350373 | MGAT2 | c.645T>C (p.Tyr215=)
| |
14 | g.49621913T>G | CA389619690 | MGAT2 | c.645T>G (p.Tyr215Ter)
| |
14 | g.49621914C>A | CA389619697 | MGAT2 | c.646C>A (p.Pro216Thr)
| |
14 | g.49621914C>G | CA389619694 | MGAT2 | c.646C>G (p.Pro216Ala)
| |
14 | g.49621914C>T | CA389619692 | MGAT2 | c.646C>T (p.Pro216Ser)
| |
14 | g.49621915C>A | CA389619700 | MGAT2 | c.647C>A (p.Pro216His)
| |
14 | g.49621915C= | CA2135804736 | MGAT2 | c.647C= (p.Pro216=)
| |
14 | g.49621915C>G | CA389619702 | MGAT2 | c.647C>G (p.Pro216Arg)
| |
14 | g.49621915C>T | CA389619704 | MGAT2 | c.647C>T (p.Pro216Leu)
| dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.49621916C>A | CA486349710 | MGAT2 | c.648C>A (p.Pro216=)
| gnomAD v4 |
14 | g.49621916C= | CA2135804737 | MGAT2 | c.648C= (p.Pro216=)
| |
14 | g.49621916C>G | CA486349709 | MGAT2 | c.648C>G (p.Pro216=)
| |
14 | g.49621916C>T | CA7172586 | MGAT2 | c.648C>T (p.Pro216=)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
14 | g.49621917G>A | CA389619707 | MGAT2 | c.649G>A (p.Asp217Asn)
| |
14 | g.49621917G>C | CA389619710 | MGAT2 | c.649G>C (p.Asp217His)
| |
14 | g.49621917G>T | CA389619712 | MGAT2 | c.649G>T (p.Asp217Tyr)
| gnomAD v4 |
14 | g.49621918A= | CA2135804738 | MGAT2 | c.650A= (p.Asp217=)
| |
14 | g.49621918A>C | CA389619713 | MGAT2 | c.650A>C (p.Asp217Ala)
| |
14 | g.49621918A>G | CA389619714 | MGAT2 | c.650A>G (p.Asp217Gly)
| |
14 | g.49621918A>T | CA389619716 | MGAT2 | c.650A>T (p.Asp217Val)
| dbSNP |
14 | g.49621919C>A | CA389619718 | MGAT2 | c.651C>A (p.Asp217Glu)
| |
14 | g.49621919C= | CA2135804739 | MGAT2 | c.651C= (p.Asp217=)
| |
14 | g.49621919C>G | CA389619719 | MGAT2 | c.651C>G (p.Asp217Glu)
| |
14 | g.49621919C>T | CA7172587 | MGAT2 | c.651C>T (p.Asp217=)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
14 | g.49621920T>A | CA389619727 | MGAT2 | c.652T>A (p.Ser218Thr)
| |
14 | g.49621920T>C | CA389619725 | MGAT2 | c.652T>C (p.Ser218Pro)
| |
14 | g.49621920T>G | CA389619722 | MGAT2 | c.652T>G (p.Ser218Ala)
| |
14 | g.49621921C>A | CA389619728 | MGAT2 | c.653C>A (p.Ser218Tyr)
| |
14 | g.49621921C>G | CA389619731 | MGAT2 | c.653C>G (p.Ser218Cys)
| |
14 | g.49621921C>T | CA389619734 | MGAT2 | c.653C>T (p.Ser218Phe)
| |
14 | g.49621922C>A | CA486349716 | MGAT2 | c.654C>A (p.Ser218=)
| |
14 | g.49621922C>G | CA486349718 | MGAT2 | c.654C>G (p.Ser218=)
| |
14 | g.49621922C>T | CA486349717 | MGAT2 | c.654C>T (p.Ser218=)
| dbSNP |
14 | g.49621923T>A | CA389619735 | MGAT2 | c.655T>A (p.Phe219Ile)
| |
14 | g.49621923T>C | CA7172588 | MGAT2 | c.655T>C (p.Phe219Leu)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.49621923T>G | CA389619737 | MGAT2 | c.655T>G (p.Phe219Val)
| |
14 | g.49621923T= | CA2135804740 | MGAT2 | c.655T= (p.Phe219=)
| |
14 | g.49621924T>A | CA389619744 | MGAT2 | c.656T>A (p.Phe219Tyr)
| |
14 | g.49621924T>C | CA389619739 | MGAT2 | c.656T>C (p.Phe219Ser)
| |
14 | g.49621924T>G | CA389619742 | MGAT2 | c.656T>G (p.Phe219Cys)
| |
14 | g.49621925C>A | CA389619747 | MGAT2 | c.657C>A (p.Phe219Leu)
| |
14 | g.49621925C= | CA2135804741 | MGAT2 | c.657C= (p.Phe219=)
| |
14 | g.49621925C>G | CA389619750 | MGAT2 | c.657C>G (p.Phe219Leu)
| |
14 | g.49621925C>T | CA486349723 | MGAT2 | c.657C>T (p.Phe219=)
| dbSNP gnomAD v4 |
14 | g.49621926G>A | CA389619752 | MGAT2 | c.658G>A (p.Gly220Ser)
| dbSNP |
14 | g.49621926G>C | CA389619754 | MGAT2 | c.658G>C (p.Gly220Arg)
| |
14 | g.49621926G= | CA2135804742 | MGAT2 | c.658G= (p.Gly220=)
| |
14 | g.49621926G>T | CA389619755 | MGAT2 | c.658G>T (p.Gly220Cys)
| gnomAD v4 |
14 | g.49621927G>A | CA389619758 | MGAT2 | c.659G>A (p.Gly220Asp)
| gnomAD v4 |
14 | g.49621927G>C | CA389619761 | MGAT2 | c.659G>C (p.Gly220Ala)
| |
14 | g.49621927G>T | CA389619759 | MGAT2 | c.659G>T (p.Gly220Val)
| |
14 | g.49621927_49621928dup | CA7172589 | MGAT2 | c.659_660dup (p.His221AlafsTer26)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
14 | g.49621928C>A | CA486349725 | MGAT2 | c.660C>A (p.Gly220=)
| |
14 | g.49621928C= | CA2135804743 | MGAT2 | c.660C= (p.Gly220=)
| |
14 | g.49621928C>G | CA486349726 | MGAT2 | c.660C>G (p.Gly220=)
| |
14 | g.49621928C>T | CA7172590 | MGAT2 | c.660C>T (p.Gly220=)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.49621929C>A | CA389619766 | MGAT2 | c.661C>A (p.His221Asn)
| |
14 | g.49621929C>G | CA389619767 | MGAT2 | c.661C>G (p.His221Asp)
| |
14 | g.49621929C>T | CA389619769 | MGAT2 | c.661C>T (p.His221Tyr)
| |
14 | g.49621930A= | CA2135804744 | MGAT2 | c.662A= (p.His221=)
| |
14 | g.49621930A>C | CA389619772 | MGAT2 | c.662A>C (p.His221Pro)
| |
14 | g.49621930A>G | CA7172591 | MGAT2 | c.662A>G (p.His221Arg)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
14 | g.49621930A>T | CA389619775 | MGAT2 | c.662A>T (p.His221Leu)
| gnomAD v4 |
14 | g.49621931T>A | CA389619778 | MGAT2 | c.663T>A (p.His221Gln)
| |
14 | g.49621931T>C | CA486349731 | MGAT2 | c.663T>C (p.His221=)
| dbSNP gnomAD v2 gnomAD v4 |
14 | g.49621931T>G | CA389619781 | MGAT2 | c.663T>G (p.His221Gln)
| |
14 | g.49621931T= | CA2135804745 | MGAT2 | c.663T= (p.His221=)
| |
14 | g.49621932T>A | CA389619782 | MGAT2 | c.664T>A (p.Tyr222Asn)
| |
14 | g.49621932T>C | CA389619784 | MGAT2 | c.664T>C (p.Tyr222His)
| |
14 | g.49621932T>G | CA389619787 | MGAT2 | c.664T>G (p.Tyr222Asp)
| |
14 | g.49621933A>C | CA389619790 | MGAT2 | c.665A>C (p.Tyr222Ser)
| |
14 | g.49621933A>G | CA389619793 | MGAT2 | c.665A>G (p.Tyr222Cys)
| gnomAD v4 |
14 | g.49621933A>T | CA389619791 | MGAT2 | c.665A>T (p.Tyr222Phe)
| |
14 | g.49621934T>A | CA389619795 | MGAT2 | c.666T>A (p.Tyr222Ter)
| |
14 | g.49621934T>C | CA260660756 | MGAT2 | c.666T>C (p.Tyr222=)
| dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.49621934T>G | CA389619798 | MGAT2 | c.666T>G (p.Tyr222Ter)
| |
14 | g.49621934T= | CA2135804746 | MGAT2 | c.666T= (p.Tyr222=)
| |
14 | g.49621935A>C | CA486349737 | MGAT2 | c.667A>C (p.Arg223=)
| |
14 | g.49621935A>G | CA389619801 | MGAT2 | c.667A>G (p.Arg223Gly)
| |
14 | g.49621935A>T | CA389619802 | MGAT2 | c.667A>T (p.Arg223Ter)
| |
14 | g.49621939_49621940del | CA2624726677 | MGAT2 | c.671_672del (p.Glu224GlyfsTer?)
| gnomAD v4 |
14 | g.49621936G>A | CA389619804 | MGAT2 | c.668G>A (p.Arg223Lys)
| |
14 | g.49621936G>C | CA389619807 | MGAT2 | c.668G>C (p.Arg223Thr)
| |
14 | g.49621936G>T | CA389619809 | MGAT2 | c.668G>T (p.Arg223Ile)
| |
14 | g.49621937A>C | CA389619812 | MGAT2 | c.669A>C (p.Arg223Ser)
| |
14 | g.49621937A>G | CA486349738 | MGAT2 | c.669A>G (p.Arg223=)
| |
14 | g.49621937A>T | CA389619813 | MGAT2 | c.669A>T (p.Arg223Ser)
| |
14 | g.49621938G>A | CA389619816 | MGAT2 | c.670G>A (p.Glu224Lys)
| |
14 | g.49621938G>C | CA389619818 | MGAT2 | c.670G>C (p.Glu224Gln)
| |
14 | g.49621938G>T | CA389619820 | MGAT2 | c.670G>T (p.Glu224Ter)
| |
14 | g.49621939A= | CA2135804747 | MGAT2 | c.671A= (p.Glu224=)
| |
14 | g.49621939A>C | CA389619828 | MGAT2 | c.671A>C (p.Glu224Ala)
| |
14 | g.49621939A>G | CA389619822 | MGAT2 | c.671A>G (p.Glu224Gly)
| dbSNP gnomAD v3 gnomAD v4 |
14 | g.49621939A>T | CA389619824 | MGAT2 | c.671A>T (p.Glu224Val)
| |
14 | g.49621940G>A | CA486349742 | MGAT2 | c.672G>A (p.Glu224=)
| dbSNP gnomAD v4 |
14 | g.49621940G>C | CA389619830 | MGAT2 | c.672G>C (p.Glu224Asp)
| |
14 | g.49621940G= | CA2135804748 | MGAT2 | c.672G= (p.Glu224=)
| |
14 | g.49621940G>T | CA389619832 | MGAT2 | c.672G>T (p.Glu224Asp)
| |
14 | g.49621941G>A | CA389619834 | MGAT2 | c.673G>A (p.Ala225Thr)
| dbSNP gnomAD v4 |
14 | g.49621941G>C | CA389619836 | MGAT2 | c.673G>C (p.Ala225Pro)
| |
14 | g.49621941G= | CA2135804749 | MGAT2 | c.673G= (p.Ala225=)
| |
14 | g.49621941G>T | CA389619837 | MGAT2 | c.673G>T (p.Ala225Ser)
| |
14 | g.49621942C>A | CA389619839 | MGAT2 | c.674C>A (p.Ala225Asp)
| |
14 | g.49621942C>G | CA389619841 | MGAT2 | c.674C>G (p.Ala225Gly)
| |
14 | g.49621942C>T | CA389619843 | MGAT2 | c.674C>T (p.Ala225Val)
| |
14 | g.49621943C>A | CA486349745 | MGAT2 | c.675C>A (p.Ala225=)
| gnomAD v4 |
14 | g.49621943C>G | CA486349747 | MGAT2 | c.675C>G (p.Ala225=)
| |
14 | g.49621943C>T | CA486349749 | MGAT2 | c.675C>T (p.Ala225=)
| |
14 | g.49621944A>C | CA389619845 | MGAT2 | c.676A>C (p.Lys226Gln)
| |
14 | g.49621944A>G | CA389619846 | MGAT2 | c.676A>G (p.Lys226Glu)
| gnomAD v4 |
14 | g.49621944A>T | CA389619848 | MGAT2 | c.676A>T (p.Lys226Ter)
| |
14 | g.49621945A= | CA2135804750 | MGAT2 | c.677A= (p.Lys226=)
| |
14 | g.49621945A>C | CA389619852 | MGAT2 | c.677A>C (p.Lys226Thr)
| dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.49621945A>G | CA389619855 | MGAT2 | c.677A>G (p.Lys226Arg)
| dbSNP gnomAD v3 gnomAD v4 |
14 | g.49621945A>T | CA389619853 | MGAT2 | c.677A>T (p.Lys226Ile)
| gnomAD v4 |
14 | g.49621946A>C | CA389619858 | MGAT2 | c.678A>C (p.Lys226Asn)
| |
14 | g.49621946A>G | CA486349750 | MGAT2 | c.678A>G (p.Lys226=)
| |
14 | g.49621946A>T | CA389619860 | MGAT2 | c.678A>T (p.Lys226Asn)
| COSMIC |
14 | g.49621947T>A | CA389619862 | MGAT2 | c.679T>A (p.Phe227Ile)
| |
14 | g.49621947T>C | CA389619867 | MGAT2 | c.679T>C (p.Phe227Leu)
| |
14 | g.49621947T>G | CA389619864 | MGAT2 | c.679T>G (p.Phe227Val)
| |
14 | g.49621948dup | CA2839633243 | MGAT2 | c.680dup (p.Ser228LeufsTer?)
| |
14 | g.49621948T>A | CA389619870 | MGAT2 | c.680T>A (p.Phe227Tyr)
| |
14 | g.49621948T>C | CA389619875 | MGAT2 | c.680T>C (p.Phe227Ser)
| |
14 | g.49621948T>G | CA389619873 | MGAT2 | c.680T>G (p.Phe227Cys)
| |
14 | g.49621949C>A | CA389619877 | MGAT2 | c.681C>A (p.Phe227Leu)
| |
14 | g.49621949C>G | CA389619879 | MGAT2 | c.681C>G (p.Phe227Leu)
| |
14 | g.49621949C>T | CA486349754 | MGAT2 | c.681C>T (p.Phe227=)
| |
14 | g.49621950T>A | CA389619882 | MGAT2 | c.682T>A (p.Ser228Thr)
| |
14 | g.49621950T>C | CA389619885 | MGAT2 | c.682T>C (p.Ser228Pro)
| |
14 | g.49621950T>G | CA389619887 | MGAT2 | c.682T>G (p.Ser228Ala)
| |
14 | g.49621951C>A | CA389619890 | MGAT2 | c.683C>A (p.Ser228Tyr)
| |
14 | g.49621951C= | CA2135804751 | MGAT2 | c.683C= (p.Ser228=)
| |
14 | g.49621951C>G | CA389619892 | MGAT2 | c.683C>G (p.Ser228Cys)
| |
14 | g.49621951C>T | CA260660759 | MGAT2 | c.683C>T (p.Ser228Phe)
| dbSNP |
14 | g.49621953dup | CA2840280173 | MGAT2 | c.685dup (p.Gln229ProfsTer?)
| |
14 | g.49621952C>A | CA486349757 | MGAT2 | c.684C>A (p.Ser228=)
| |
14 | g.49621952C= | CA2135804752 | MGAT2 | c.684C= (p.Ser228=)
| |
14 | g.49621952C>G | CA486349758 | MGAT2 | c.684C>G (p.Ser228=)
| |
14 | g.49621952C>T | CA486349761 | MGAT2 | c.684C>T (p.Ser228=)
| dbSNP gnomAD v2 |
14 | g.49621952_49621956delinsCCAGA | CA2135804753 | MGAT2 | c.684_688delinsCCAGA (p.Ser228=)
| |
14 | g.49621953C>A | CA389619894 | MGAT2 | c.685C>A (p.Gln229Lys)
| |
14 | g.49621953C>G | CA389619897 | MGAT2 | c.685C>G (p.Gln229Glu)
| |
14 | g.49621953C>T | CA389619898 | MGAT2 | c.685C>T (p.Gln229Ter)
| |
14 | g.49621954_49621957del | CA2135804754 | MGAT2 | c.686_689del (p.Gln229ProfsTer16)
| dbSNP |
14 | g.49621954A= | CA2135804755 | MGAT2 | c.686A= (p.Gln229=)
| |
14 | g.49621954A>C | CA389619901 | MGAT2 | c.686A>C (p.Gln229Pro)
| |
14 | g.49621954A>G | CA389619905 | MGAT2 | c.686A>G (p.Gln229Arg)
| dbSNP gnomAD v2 gnomAD v4 |
14 | g.49621954A>T | CA389619903 | MGAT2 | c.686A>T (p.Gln229Leu)
| |
14 | g.49621955G>A | CA486349762 | MGAT2 | c.687G>A (p.Gln229=)
| |
14 | g.49621955G>C | CA389619907 | MGAT2 | c.687G>C (p.Gln229His)
| gnomAD v4 |
14 | g.49621955G= | CA2135804756 | MGAT2 | c.687G= (p.Gln229=)
| |
14 | g.49621955G>T | CA389619910 | MGAT2 | c.687G>T (p.Gln229His)
| dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.49621956A= | CA2135804757 | MGAT2 | c.688A= (p.Thr230=)
| |
14 | g.49621956A>C | CA389619912 | MGAT2 | c.688A>C (p.Thr230Pro)
| ClinVar dbSNP gnomAD v4 |
14 | g.49621956A>G | CA389619914 | MGAT2 | c.688A>G (p.Thr230Ala)
| |
14 | g.49621956A>T | CA389619917 | MGAT2 | c.688A>T (p.Thr230Ser)
| |
14 | g.49621957C>A | CA389619920 | MGAT2 | c.689C>A (p.Thr230Asn)
| |
14 | g.49621957C>G | CA389619922 | MGAT2 | c.689C>G (p.Thr230Ser)
| |
14 | g.49621957C>T | CA389619924 | MGAT2 | c.689C>T (p.Thr230Ile)
| |
14 | g.49621958C>A | CA486349770 | MGAT2 | c.690C>A (p.Thr230=)
| |
14 | g.49621958C>G | CA486349771 | MGAT2 | c.690C>G (p.Thr230=)
| |
14 | g.49621958C>T | CA486349769 | MGAT2 | c.690C>T (p.Thr230=)
| |
14 | g.49621959A>C | CA389619929 | MGAT2 | c.691A>C (p.Lys231Gln)
| |
14 | g.49621959A>G | CA389619931 | MGAT2 | c.691A>G (p.Lys231Glu)
| |
14 | g.49621959A>T | CA389619927 | MGAT2 | c.691A>T (p.Lys231Ter)
| |
14 | g.49621961dup | CA486349772 | MGAT2 | c.693dup (p.His232ThrfsTer?)
| COSMIC |
14 | g.49621960A>C | CA389619934 | MGAT2 | c.692A>C (p.Lys231Thr)
| |
14 | g.49621960A>G | CA389619936 | MGAT2 | c.692A>G (p.Lys231Arg)
| |
14 | g.49621960A>T | CA389619939 | MGAT2 | c.692A>T (p.Lys231Ile)
| |
14 | g.49621961A>C | CA389619941 | MGAT2 | c.693A>C (p.Lys231Asn)
| |
14 | g.49621961A>G | CA486349775 | MGAT2 | c.693A>G (p.Lys231=)
| |
14 | g.49621961A>T | CA389619942 | MGAT2 | c.693A>T (p.Lys231Asn)
| |
14 | g.49621962C>A | CA389619948 | MGAT2 | c.694C>A (p.His232Asn)
| |
14 | g.49621962C>G | CA389619944 | MGAT2 | c.694C>G (p.His232Asp)
| |
14 | g.49621962C>T | CA389619945 | MGAT2 | c.694C>T (p.His232Tyr)
| gnomAD v3 gnomAD v4 |
14 | g.49621963A= | CA2135804758 | MGAT2 | c.695A= (p.His232=)
| |
14 | g.49621963A>C | CA389619950 | MGAT2 | c.695A>C (p.His232Pro)
| COSMIC |
14 | g.49621963A>G | CA389619952 | MGAT2 | c.695A>G (p.His232Arg)
| dbSNP gnomAD v2 |
14 | g.49621963A>T | CA389619953 | MGAT2 | c.695A>T (p.His232Leu)
| |
14 | g.49621964T>A | CA389619954 | MGAT2 | c.696T>A (p.His232Gln)
| |
14 | g.49621964T>C | CA486349779 | MGAT2 | c.696T>C (p.His232=)
| |
14 | g.49621964T>G | CA389619956 | MGAT2 | c.696T>G (p.His232Gln)
| |
14 | g.49621965C>A | CA389619958 | MGAT2 | c.697C>A (p.His233Asn)
| |
14 | g.49621965C>G | CA389619963 | MGAT2 | c.697C>G (p.His233Asp)
| |
14 | g.49621965C>T | CA389619960 | MGAT2 | c.697C>T (p.His233Tyr)
| |
14 | g.49621966A= | CA2135804759 | MGAT2 | c.698A= (p.His233=)
| |
14 | g.49621966A>C | CA389619965 | MGAT2 | c.698A>C (p.His233Pro)
| |
14 | g.49621966A>G | CA260660763 | MGAT2 | c.698A>G (p.His233Arg)
| dbSNP gnomAD v3 gnomAD v4 |
14 | g.49621966A>T | CA389619969 | MGAT2 | c.698A>T (p.His233Leu)
| |
14 | g.49621967C>A | CA389619972 | MGAT2 | c.699C>A (p.His233Gln)
| |
14 | g.49621967C>G | CA389619973 | MGAT2 | c.699C>G (p.His233Gln)
| |
14 | g.49621967C>T | CA486349783 | MGAT2 | c.699C>T (p.His233=)
| gnomAD v4 |
14 | g.49621968T>A | CA389619976 | MGAT2 | c.700T>A (p.Trp234Arg)
| |
14 | g.49621968T>C | CA389619979 | MGAT2 | c.700T>C (p.Trp234Arg)
| |
14 | g.49621968T>G | CA389619980 | MGAT2 | c.700T>G (p.Trp234Gly)
| |
14 | g.49621969G>A | CA389619982 | MGAT2 | c.701G>A (p.Trp234Ter)
| gnomAD v4 |
14 | g.49621969G>C | CA389619984 | MGAT2 | c.701G>C (p.Trp234Ser)
| |
14 | g.49621969G>T | CA389619986 | MGAT2 | c.701G>T (p.Trp234Leu)
| |
14 | g.49621970G>A | CA389619990 | MGAT2 | c.702G>A (p.Trp234Ter)
| |
14 | g.49621970G>C | CA389619991 | MGAT2 | c.702G>C (p.Trp234Cys)
| |
14 | g.49621970G>T | CA389619988 | MGAT2 | c.702G>T (p.Trp234Cys)
| |
14 | g.49621971T>A | CA389619996 | MGAT2 | c.703T>A (p.Trp235Arg)
| |
14 | g.49621971T>C | CA389619993 | MGAT2 | c.703T>C (p.Trp235Arg)
| |
14 | g.49621971T>G | CA389619995 | MGAT2 | c.703T>G (p.Trp235Gly)
| |
14 | g.49621972G>A | CA389619998 | MGAT2 | c.704G>A (p.Trp235Ter)
| COSMIC |
14 | g.49621972G>C | CA389620000 | MGAT2 | c.704G>C (p.Trp235Ser)
| |
14 | g.49621972G>T | CA389620003 | MGAT2 | c.704G>T (p.Trp235Leu)
| |
14 | g.49621973G>A | CA389620013 | MGAT2 | c.705G>A (p.Trp235Ter)
| |
14 | g.49621973G>C | CA389620010 | MGAT2 | c.705G>C (p.Trp235Cys)
| |
14 | g.49621973G>T | CA389620008 | MGAT2 | c.705G>T (p.Trp235Cys)
| |
14 | g.49621974T>A | CA389620015 | MGAT2 | c.706T>A (p.Trp236Arg)
| |
14 | g.49621974T>C | CA389620017 | MGAT2 | c.706T>C (p.Trp236Arg)
| |
14 | g.49621974T>G | CA389620018 | MGAT2 | c.706T>G (p.Trp236Gly)
| |
14 | g.49621975G>A | CA389620020 | MGAT2 | c.707G>A (p.Trp236Ter)
| |
14 | g.49621975G>C | CA389620022 | MGAT2 | c.707G>C (p.Trp236Ser)
| |
14 | g.49621975G>T | CA389620024 | MGAT2 | c.707G>T (p.Trp236Leu)
| |
14 | g.49621976G>A | CA389620026 | MGAT2 | c.708G>A (p.Trp236Ter)
| |
14 | g.49621976G>C | CA389620035 | MGAT2 | c.708G>C (p.Trp236Cys)
| |
14 | g.49621976G>T | CA389620027 | MGAT2 | c.708G>T (p.Trp236Cys)
| |