111602451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 50920311-G-A

111602451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 50920311-G-T

http://identifiers.org/hco/11/GRCh38#111602603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50920134-C-A

111602603-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: missense variant
orthologous variants: 50920134-C-G

111602603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: missense variant
orthologous variants: 50920134-C-T

111602840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron_variant, undefined
orthologous variants: 50919966-G-A

111604669-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron_variant, undefined
orthologous variants: 50918302-C-G

111606065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50916899-G-A

111606569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 50916431-A-G

111606641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 50916373-C-T

111607247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50915942-A-G

111607260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50915929-T-C

111607708-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50915492-T-G

111608645-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50913837-A-T

111608786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50913713-C-T

http://identifiers.org/hco/11/GRCh38#111609119-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50913457-A-C

111609119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50913457-A-G

111609119-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50913457-A-T

111609156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50913417-T-C

111615691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50910536-A-G

111616152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50910002-T-C

http://identifiers.org/hco/11/GRCh38#111616161-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50909991-A-C

111616161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50909991-A-G

111616170-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50909982-A-T

http://identifiers.org/hco/11/GRCh38#111616264-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50909893-A-C

111616436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50909724-T-C

111616704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50909621-G-A

111616854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50909550-A-G

111616993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50909458-A-G

111617591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50908854-C-T

111617761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50908713-A-G

111617784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50908704-G-T

111617832-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50908642-T-A

111617832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50908642-T-C

111619219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50908284-T-C

111620023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50907263-A-G

111620109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50907184-T-C

111620222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50907077-G-T

http://identifiers.org/hco/11/GRCh38#111620291-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50907011-A-C

111620291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50907011-A-G

111620425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50906883-T-C

111620462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50906846-G-T

http://identifiers.org/hco/11/GRCh38#111620482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50906825-C-A

111620482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50906825-C-T

111625771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50904040-A-G

111625829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50903921-G-A

111627802-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50902773-A-T

111627831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50902744-T-C

111627912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50902664-A-G

111628119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50902295-A-G

111628815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50901563-T-C

111629541-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50900757-G-C

111629615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50900686-G-A

111629735-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50900259-A-T

111629756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50900238-A-G

111629963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50900036-G-A

111630217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50899792-A-G

111633070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50899456-A-G

http://identifiers.org/hco/11/GRCh38#111633092-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50899434-A-C

111633441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron_variant, undefined
orthologous variants: 50898240-T-C

111633733-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50897961-G-C

111634317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50897436-G-A

111634323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50897430-T-C

111634720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50897073-C-T

111635963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50896236-C-T

111636242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50895978-G-A

111636356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50895889-C-T

http://identifiers.org/hco/11/GRCh38#111636364-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50895881-C-A

111637869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50894281-T-C

111637879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50894270-G-A

111637938-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50894203-T-G

111637941-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50894200-T-G

111638023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50894120-A-G

111638346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50893791-C-T

111639033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50893091-G-A

111639070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50892982-A-G

111639390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50892690-A-G

111639945-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50891664-C-G

111639952-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50891657-T-A

111639955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50891654-A-G

111640077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50891533-C-T

111640397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50891193-A-G

111640427-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50891163-C-G

111641004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50890861-G-A

111641907-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50888939-A-T

111641933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50888913-T-C

111642192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50888667-A-G

111642340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50888548-A-G

111642393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50888517-G-A

111642499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50888411-T-C

111648150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50887078-T-C

111648207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50887042-T-C

111648365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50886888-C-T

111648595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50886650-C-T

111648601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50886644-G-T

111649174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50886147-G-A

111649243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50886078-A-G

http://identifiers.org/hco/11/GRCh38#111649274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50886047-C-A

111650691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50884641-T-C

111651109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50884237-A-G

111651218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50884135-T-C

111651806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50883356-A-G

111653829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50881650-C-T

111654565-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50880963-T-A

111654878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50880637-G-A

http://identifiers.org/hco/11/GRCh38#111655683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50880064-C-A

111656440-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50879491-G-C

111656709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50879225-T-C

111657256-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50878088-T-G

111657717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50877940-A-G

111657740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50877917-G-A

111657859-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50877803-A-T

111659169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50877218-G-T

111659680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50876820-C-T

111659930-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50876294-T-G

111660282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50875999-G-A

111660745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50872958-A-G

111661157-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50872710-C-G

111663276-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50871161-T-G

111663427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50871041-G-A

111663504-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50870976-G-C

111663925-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50870447-T-A

111663963-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50870400-T-G

http://identifiers.org/hco/11/GRCh38#111664708-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50869970-A-C

111669351-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50865792-G-C

111669519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50865654-C-T

111670170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50865418-T-C

http://identifiers.org/hco/11/GRCh38#111670226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50865381-C-A

111670226-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50865381-C-G

111670232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50865375-G-T

111670467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50865140-T-C

111670545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50865063-A-G

111670624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50864987-G-T

111670654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50864957-A-G

111672993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50863879-G-A

http://identifiers.org/hco/11/GRCh38#111673081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50863801-C-A

111673447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50862605-G-T

111674325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50861871-A-G

111674541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50861655-C-T

111675303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50861237-T-C

111677307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50859966-T-C

111678466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50858803-C-T

111678585-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50858671-T-A

111678606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50858648-T-C

111678788-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50858527-T-G

111679390-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50857826-C-G

111680588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50855129-T-C

111680935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50854807-G-A

http://identifiers.org/hco/11/GRCh38#111681004-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50854745-A-C

111686005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: -T-C

111686068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: -T-C

111686588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50847607-T-C

http://identifiers.org/hco/11/GRCh38#111688232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50846644-C-A

111688232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50846644-C-T

111692802-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50838527-A-T

111692880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50838464-A-G

111692891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50838456-A-G

http://identifiers.org/hco/11/GRCh38#111693597-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50837907-A-C

111693597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50837907-A-G

111693597-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50837907-A-T

111693617-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50837887-A-T

111693655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50837632-C-T

111693746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50837541-G-A

111694057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50837261-A-G

111694132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50837188-C-T

111694476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50836036-C-T

111695023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50835562-T-C

111695045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 50835540-T-C

111695053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 50835532-G-T

111695180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50835403-G-A

111695285-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50834543-A-T

111698221-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50830940-G-C

111698221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50830940-G-T

111698768-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50830706-C-G

111698836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 50830636-A-G

http://identifiers.org/hco/11/GRCh38#111699772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50829818-C-A

111699868-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50829729-T-G

111699923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50829681-C-T

111700256-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50829382-A-T

111700424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50829225-G-T

111700754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50829070-A-G

111701043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50828796-A-G

111701045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50828794-C-T

111701121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50828743-T-C

111701128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50828736-T-C

111701165-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50828699-G-C

http://identifiers.org/hco/11/GRCh38#111701330-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50828551-A-C

111701390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50828493-A-G

111701407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50828478-T-C

111701407-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50828478-T-G

111702132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50827829-G-A

111702807-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50827529-C-G

111702823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50827515-C-T

111702997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50827151-C-T

111703322-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron_variant, missense_variant
orthologous variants: 50826841-T-G

111703416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron_variant, missense_variant
orthologous variants: 50826747-C-T

111703636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50826541-A-G

111703989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50826105-A-G

111704103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50826051-G-A

111704638-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50825523-T-A

111704928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50824893-G-A

111704928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50824893-G-T

111704943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50824878-G-A

111704943-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50824878-G-C

111704943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50824878-G-T

111704944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50824877-G-T

http://identifiers.org/hco/11/GRCh38#111704969-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50824852-A-C

111704969-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50824852-A-T

111705259-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50824560-T-A

http://identifiers.org/hco/11/GRCh38#111705283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50824535-C-A

111705283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50824535-C-T

111707008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50823074-T-C

111707197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron_variant, undefined
orthologous variants: 50822872-G-A

111707248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron_variant, undefined
orthologous variants: 50822836-C-T

111709765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50821080-A-G

111709972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50820717-T-C

111710782-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50819891-T-A

111711684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50819306-G-A

http://identifiers.org/hco/11/GRCh38#111711929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50819110-C-A

http://identifiers.org/hco/11/GRCh38#111712070-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50818963-A-C

111712070-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50818963-A-T

111712169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50818911-G-T

http://identifiers.org/hco/11/GRCh38#111712522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50818582-C-A

111712522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50818582-C-T

111712595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50818534-C-T

111712596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50818533-G-A

111712858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50818272-G-T

111713364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50818088-G-A

111714173-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50817639-G-C

111714339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50817485-T-C

111714592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50817268-T-C

111715102-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50816762-G-C

111715174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50816694-C-T

111715429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50816489-T-C

111718264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50812218-G-A

111718767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50811797-G-A

http://identifiers.org/hco/11/GRCh38#111718780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50811784-C-A

111719204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50811370-T-C

http://identifiers.org/hco/11/GRCh38#111719340-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50811241-A-C

111719340-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50811241-A-T

http://identifiers.org/hco/11/GRCh38#111719342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50811239-C-A

111719342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50811239-C-T

111719348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50811233-G-T

http://identifiers.org/hco/11/GRCh38#111719378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50811217-C-A

111719378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50811217-C-T

111719448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50811152-A-G

111719448-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50811152-A-T

http://identifiers.org/hco/11/GRCh38#111719505-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50811102-A-C

111719505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50811102-A-G

http://identifiers.org/hco/11/GRCh38#111720063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50810560-C-A

111720063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50810560-C-T

111720298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50810345-T-C

111720383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50810161-G-A

111721207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50809365-T-C

111721561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50809041-A-G

111721643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50808950-A-G

111721757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50808847-G-A

111721757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50808847-G-T

http://identifiers.org/hco/11/GRCh38#111721953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50808659-C-A

111721953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50808659-C-T

111721955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50808657-T-C

111722023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50808620-G-A

111722023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50808620-G-T

111722034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50808609-G-T

111722525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50808183-G-A

111722525-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50808183-G-C

111722525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50808183-G-T

111722569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50808143-G-T

http://identifiers.org/hco/11/GRCh38#111722583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50808129-C-A

111722589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50808123-G-A

111722589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50808123-G-T

http://identifiers.org/hco/11/GRCh38#111722635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50808063-C-A

111722635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50808063-C-T

111722688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 50808010-C-T

111722716-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron_variant, missense_variant
orthologous variants: 50807982-G-C

111722766-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50807934-G-C

111722805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50807895-T-C

111722871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50807861-G-T

111723380-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron variant
orthologous variants: 50807356-T-A

111723764-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron_variant, missense_variant
orthologous variants: 50806991-T-A

111723764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron_variant, missense_variant
orthologous variants: 50806991-T-C

http://identifiers.org/hco/11/GRCh38#111723821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50806931-C-A

111724129-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: intron_variant, undefined
orthologous variants: 50806623-G-C

111724144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50806609-T-C

111724151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50806602-G-A

http://identifiers.org/hco/11/GRCh38#111724195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50806558-C-A

111724195-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50806558-C-G

111724245-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50806509-C-G

111724245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50806509-C-T

111724270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50806486-G-T

111724353-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50806407-G-C

111724353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50806407-G-T

111724381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50806379-G-A

111724381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50806379-G-T

111724419-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50806341-T-A

111724419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50806341-T-C

111724419-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50806341-T-G

111724516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50806254-T-C

http://identifiers.org/hco/11/GRCh38#111724538-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50806232-A-C

111724538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50806232-A-G

http://identifiers.org/hco/11/GRCh38#111724563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50806204-C-A

111724563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50806204-C-T

111724681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50806159-A-G

111724743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50806097-A-G

http://identifiers.org/hco/11/GRCh38#111724780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50806071-C-A

111724780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50806071-C-T

http://identifiers.org/hco/11/GRCh38#111724908-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50805951-A-C

111725027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50805866-T-C

111725548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50805414-G-A

111725548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50805414-G-T

111725590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50805373-T-C

http://identifiers.org/hco/11/GRCh38#111725654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50805310-C-A

111725654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50805310-C-T

111725672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50805288-A-G

111725682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50805279-T-C

111725749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50805202-C-T

111725874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50805072-G-T

http://identifiers.org/hco/11/GRCh38#111725887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50805059-C-A

111726004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50804948-G-A

111726004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50804948-G-T

111726274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50804699-G-A

111726401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50804573-G-A

111726488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50804488-G-A

111726488-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50804488-G-C

111726488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50804488-G-T

http://identifiers.org/hco/11/GRCh38#111726576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50804404-C-A

111726576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50804404-C-T

http://identifiers.org/hco/11/GRCh38#111726588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50804392-C-A

111726588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50804392-C-T

http://identifiers.org/hco/11/GRCh38#111726660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50804344-C-A

http://identifiers.org/hco/11/GRCh38#111726689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50804315-C-A

http://identifiers.org/hco/11/GRCh38#111726709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50804296-C-A

111726709-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50804296-C-G

111726709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50804296-C-T

111726747-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50804266-T-A

111727041-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 50803970-A-T

111727092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50803909-G-A

111727092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50803909-G-T

111727351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50803653-G-A

111727351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50803653-G-T

111727389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50803630-G-A

http://identifiers.org/hco/11/GRCh38#111727504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50803548-C-A

111727506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50803546-T-C

http://identifiers.org/hco/11/GRCh38#111727603-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50803464-A-C

111727603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50803464-A-G

111727603-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50803464-A-T

111727644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50803437-A-G

http://identifiers.org/hco/11/GRCh38#111727660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50803421-C-A

111727660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50803421-C-T

111727773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50803360-A-G

111727793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50803341-A-G

111727954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50803195-A-G

111727980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50803171-T-C

111728087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 50803041-T-C

111728259-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50802870-T-G

111728642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50802798-G-T

111729069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50802693-G-A

http://identifiers.org/hco/11/GRCh38#111729230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50802504-C-A

111729230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50802504-C-T

111729423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50802365-C-T

111729435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50802353-A-G

111729436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50802352-T-C

http://identifiers.org/hco/11/GRCh38#111729734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50802176-C-A

111729734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50802176-C-T

111729821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50802105-G-T

111729823-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50802103-G-C

http://identifiers.org/hco/11/GRCh38#111729940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50801971-C-A

111729940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50801971-C-T

111730032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50801882-T-C

111730035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50801879-G-A

111730035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50801879-G-T

111730077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50801665-G-A

http://identifiers.org/hco/11/GRCh38#111730155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50801581-C-A

http://identifiers.org/hco/11/GRCh38#111730559-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50801231-A-C

111730559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50801231-A-G

111730792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21680
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50801005-A-G