28020861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: 3 prime UTR variant
orthologous variants: 109171853-G-A

http://identifiers.org/hco/11/GRCh38#28021359-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#109171427-A-C

28021396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109171397-C-T

28023251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109169628-T-C

http://identifiers.org/hco/11/GRCh38#28023709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#109169051-C-A

28023709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109169051-C-T

28023842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: stop gained
orthologous variants: 109168918-G-T

28023902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109168866-G-A

28023902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109168866-G-T

http://identifiers.org/hco/11/GRCh38#28023905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#109168863-C-A

http://identifiers.org/hco/11/GRCh38#28023996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#109168776-C-A

28023996-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109168776-C-G

28023996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109168776-C-T

28024027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109168755-T-C

http://identifiers.org/hco/11/GRCh38#28024183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#109168622-C-A

28024183-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109168622-C-G

28026340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109168379-T-C

http://identifiers.org/hco/11/GRCh38#28026699-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#109168022-A-C

28035274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109164873-G-A

28035313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109164841-A-G

28035320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109164834-T-C

28035320-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109164834-T-G

28035362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109164796-C-T

28035447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: missense variant
orthologous variants: 109164711-C-T

28035511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109164647-A-G

28035511-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109164647-A-T

28035721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109164460-T-C

28035721-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109164460-T-G

28035799-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109164394-T-G

28035828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109164365-A-G

28036337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: missense variant
orthologous variants: 109163896-T-C

28036337-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: missense variant
orthologous variants: 109163896-T-G

28036367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: missense variant
orthologous variants: 109163869-C-T

28036392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: missense variant
orthologous variants: 109163844-T-C

28036392-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: missense variant
orthologous variants: 109163844-T-G

28036395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: missense variant
orthologous variants: 109163841-T-C

http://identifiers.org/hco/11/GRCh38#28036431-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#109163826-A-C

28036646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: missense variant
orthologous variants: 109163617-G-A

28036646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: missense variant
orthologous variants: 109163617-G-T

28036712-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109163546-T-G

http://identifiers.org/hco/11/GRCh38#28036791-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#109163480-A-C

28038064-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109163130-C-G

28038341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109162884-T-C

http://identifiers.org/hco/11/GRCh38#28038627-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#109162595-A-C

28038633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109162589-C-T

28038653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109162568-T-C

28039098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109162149-A-G

28039262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109161969-C-T

28039376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109161862-T-C

28039702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109161560-C-T

28040092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109161227-A-G

28040493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109160860-T-C

28045389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109159598-G-A

28045395-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109159592-A-T

28045417-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109159588-T-A

28045483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109159542-G-T

28047402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109158554-T-C

28047769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109158194-T-C

28047960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109157912-G-A

28047996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109157877-G-A

28049352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109156351-T-C

28049650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, undefined
orthologous variants: 109156049-T-C

28049966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109155527-A-G

28049966-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109155527-A-T

http://identifiers.org/hco/11/GRCh38#28050099-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#109155371-A-C

28050129-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109155341-T-G

28050130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109155340-G-T

28050486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109155005-A-G

28050627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109154842-G-A

28050697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109154776-A-G

28051030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109154393-G-A

28051430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109153903-G-T

28051538-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109153765-A-T

28051864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109153531-T-C

http://identifiers.org/hco/11/GRCh38#28051990-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#109153404-A-C

28052276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109153226-C-T

28052310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109153192-G-A

http://identifiers.org/hco/11/GRCh38#28052344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#109153171-C-A

28052739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109152719-G-A

28052791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109152674-G-A

28052795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109152670-G-T

28052888-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109152577-G-C

28054820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109151482-T-C

28054820-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109151482-T-G

28054896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109151419-T-C

28054914-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109151405-T-A

28054914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109151405-T-C

28054955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109151324-G-A

28055079-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109151205-T-A

28055194-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109151058-C-G

28055418-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109150658-A-T

28057728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109149225-G-A

28057804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109149156-C-T

28059113-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: missense variant
orthologous variants: 109148266-T-A

28059113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: synonymous variant
orthologous variants: 109148266-T-C

28059215-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109148167-T-A

28059216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109148166-T-C

http://identifiers.org/hco/11/GRCh38#28062308-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#109141111-A-C

28062308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109141111-A-G

28062382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109141024-T-C

http://identifiers.org/hco/11/GRCh38#28062601-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#109140808-A-C

28062802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109140627-T-C

28063363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109139378-A-G

28063363-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109139378-A-T

28063383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109139357-C-T

28069062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109137585-A-G

28069063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109137584-T-C

28069113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109137541-A-G

28069113-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109137541-A-T

28069129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109137525-T-C

28069129-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109137525-T-G

28069153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109137483-G-A

28069153-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109137483-G-C

28069153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109137483-G-T

28069352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: synonymous variant
orthologous variants: 109137264-C-T

28069518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109137102-G-A

28069518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109137102-G-T

28069998-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109136695-G-C

28070415-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109136169-T-A

28070436-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109136148-T-G

28070497-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109136094-T-A

28071076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109135559-T-C

28071137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109135529-C-T

28071670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109135227-A-G

28071773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109135128-T-C

http://identifiers.org/hco/11/GRCh38#28071869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#109135040-C-A

28071904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron variant
orthologous variants: 109135002-G-T

http://identifiers.org/hco/11/GRCh38#28076962-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#109133353-A-C

28076962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109133353-A-G

28076962-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109133353-A-T

28076965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109133350-T-C

28076965-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109133350-T-G

28076997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109133318-T-C

http://identifiers.org/hco/11/GRCh38#28077014-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#109133301-A-C

28077014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109133301-A-G

28077014-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109133301-A-T

28077040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109133275-T-C

28077044-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109133271-T-A

28077044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109133271-T-C

28077065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109133250-T-C

28077077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109133238-A-G

28077078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109133237-G-A

28077078-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109133237-G-T

28077089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109133226-T-C

http://identifiers.org/hco/11/GRCh38#28077200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#109133115-C-A

28077200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109133115-C-T

28077427-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109132991-G-C

28077599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109132853-G-A

28077612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109132840-C-T

28077667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109132786-G-A

28077961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109132535-C-T

28078645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109131076-C-T

28078945-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109130819-A-T

28079214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109130190-A-G

http://identifiers.org/hco/11/GRCh38#28079249-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#109130160-A-C

http://identifiers.org/hco/11/GRCh38#28082847-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#109128800-A-C

28082847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109128800-A-G

28082847-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109128800-A-T

28082850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109128798-G-A

28082850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109128798-G-T

28082997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109128653-A-G

28082997-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109128653-A-T

28083033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109128607-A-G

28083033-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109128607-A-T

28083123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109128525-A-G

28083283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109128393-A-G

http://identifiers.org/hco/11/GRCh38#28083291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#109128385-C-A

28083291-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109128385-C-G

28083627-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109128045-T-G

28083970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109127737-A-G

28084031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109127678-T-C

28084451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109127304-A-G

28084451-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109127304-A-T

http://identifiers.org/hco/11/GRCh38#28084489-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#109127277-A-C

28084489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109127277-A-G

28084489-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109127277-A-T

http://identifiers.org/hco/11/GRCh38#28084600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#109127171-C-A

28084600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109127171-C-T

28084612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109127159-G-A

28084612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109127159-G-T

28084866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109126908-A-G

http://identifiers.org/hco/11/GRCh38#28084876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#109126898-C-A

28084876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109126898-C-T

28087993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109126055-A-G

28088403-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109125643-A-T

28088792-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109125217-T-A

28088792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109125217-T-C

28089103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109124936-A-G

28089103-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109124936-A-T

28089152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109124909-C-T

28089873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109124302-A-G

28090293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109123872-G-A

28090633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109123408-G-T

28090645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109123396-G-A

28090645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109123396-G-T

28090747-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109123296-A-T

28090814-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109122950-T-A

28090860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109122904-C-T

28090865-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109122899-T-A

28090865-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109122899-T-G

28091186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109122799-G-A

28091220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109122770-G-A

28091220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109122770-G-T

28091323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109122594-G-T

http://identifiers.org/hco/11/GRCh38#28091350-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#109122568-A-C

28091403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109122518-A-G

28091403-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109122518-A-T

28091494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109122427-C-T

28093954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109120873-C-T

28094249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109120559-T-C

28094253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109120553-G-A

28094518-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109120306-A-T

28094519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109120305-T-C

28094546-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109120278-A-T

http://identifiers.org/hco/11/GRCh38#28094822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#109120000-C-A

28094822-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109120000-C-G

28094837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109119982-T-C

28096546-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109119239-T-G

28096779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109119037-T-C

28097351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109118773-G-A

28097351-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109118773-G-C

28097351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109118773-G-T

http://identifiers.org/hco/11/GRCh38#28097469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#109118672-C-A

28097469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109118672-C-T

http://identifiers.org/hco/11/GRCh38#28097490-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#109118652-A-C

28097490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109118652-A-G

28097501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109118643-T-C

28097501-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109118643-T-G

http://identifiers.org/hco/11/GRCh38#28097518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#109118626-C-A

28097518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109118626-C-T

28097581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109118551-G-T

28097655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109118477-A-G

28097955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 109118177-T-C

28097955-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 109118177-T-G

28098436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109117806-T-C

28098436-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109117806-T-G

28098523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109117721-G-A

http://identifiers.org/hco/11/GRCh38#28098531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#109117714-C-A

28098728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109117547-G-T

28098776-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109117524-C-G

28098776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109117524-C-T

28098809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109117491-A-G

28103105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109113306-A-G

28105910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109112509-C-T

28106325-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109112337-C-G

http://identifiers.org/hco/11/GRCh38#28106508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#109112202-C-A

28106508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109112202-C-T

28106618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109112117-T-C

28106619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109112116-G-A

http://identifiers.org/hco/11/GRCh38#28107375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#109111787-C-A

http://identifiers.org/hco/11/GRCh38#28107468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#109111725-C-A

28107468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109111725-C-T

28107487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 109111706-A-G

28107496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109111701-G-A

28107737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29441
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109111513-C-T