44270512-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 45860555-A-T

44270524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 45860543-G-A

44270524-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 45860543-G-C

44270524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 45860543-G-T

http://identifiers.org/hco/6/GRCh38#44270570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#45860491-C-A

http://identifiers.org/hco/6/GRCh38#44270571-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#45860490-A-C

http://identifiers.org/hco/6/GRCh38#44270590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#45860476-C-A

44270722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 45860344-T-C

44270722-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 45860344-T-G

http://identifiers.org/hco/6/GRCh38#44270831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#45860238-C-A

44270831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, missense_variant
orthologous variants: 45860238-C-T

http://identifiers.org/hco/6/GRCh38#44270896-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#45860188-C-A

44270896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45860188-C-T

44270899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45860185-T-C

44270899-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45860185-T-G

http://identifiers.org/hco/6/GRCh38#44270934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#45860149-C-A

44270934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: 45860149-C-T

44271056-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: 45860026-C-G

44271056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: 45860026-C-T

44271086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45859996-T-C

44271163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45859919-T-C

44271265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45859837-T-C

44271348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45859751-G-T

44271488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45859557-A-G

44271627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45859424-G-A

44271914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45859131-G-A

44272346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45858797-C-T

44272550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45858592-G-T

44272825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45858334-C-T

44272866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45858296-C-T

http://identifiers.org/hco/6/GRCh38#44272935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#45858232-C-A

44272935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45858232-C-T

44272959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45858219-T-C

44272969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45858209-G-A

44272969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45858209-G-T

http://identifiers.org/hco/6/GRCh38#44272999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#45858180-C-A

44272999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45858180-C-T

http://identifiers.org/hco/6/GRCh38#44273010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#45858169-C-A

44273010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45858169-C-T

http://identifiers.org/hco/6/GRCh38#44273069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#45858122-C-A

44273069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, missense_variant
orthologous variants: 45858122-C-T

http://identifiers.org/hco/6/GRCh38#44273078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#45858113-C-A

44273078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, stop_gained
orthologous variants: 45858113-C-T

44273240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, missense_variant
orthologous variants: 45857951-C-T

http://identifiers.org/hco/6/GRCh38#44273291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#45857900-C-A

44273291-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, missense_variant
orthologous variants: 45857900-C-G

44273291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, missense_variant
orthologous variants: 45857900-C-T

44273303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, missense_variant
orthologous variants: 45857888-G-A

44273303-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, missense_variant
orthologous variants: 45857888-G-C

http://identifiers.org/hco/6/GRCh38#44273411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#45857780-C-A

44273511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45857680-G-A

44273549-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45857640-T-A

44273549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45857640-T-C

44273549-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45857640-T-G

44273554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45857635-C-T

44273578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45857611-C-T

http://identifiers.org/hco/6/GRCh38#44273626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#45857581-C-A

44273626-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45857581-C-G

44273720-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45857522-C-G

44273720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45857522-C-T

44275335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45856933-T-C

44275335-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45856933-T-G

44275347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45856921-A-G

44275484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, missense_variant
orthologous variants: 45856797-A-G

44275598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, missense_variant
orthologous variants: 45856683-G-T

44275736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, missense_variant
orthologous variants: 45856545-G-A

44275805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, missense_variant
orthologous variants: 45856476-T-C

44276132-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, missense_variant
orthologous variants: 45856149-T-A

44276132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, missense_variant
orthologous variants: 45856149-T-C

44276220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, missense_variant
orthologous variants: 45856061-G-A

44276220-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, missense_variant
orthologous variants: 45856061-G-C

44276220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, missense_variant
orthologous variants: 45856061-G-T

44276225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, missense_variant
orthologous variants: 45856056-G-A

44276225-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, missense_variant
orthologous variants: 45856056-G-C

44276225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, missense_variant
orthologous variants: 45856056-G-T

http://identifiers.org/hco/6/GRCh38#44276531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#45855747-C-A

44276531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45855747-C-T

44276595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45855678-A-G

44276633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45855640-G-A

44276634-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45855639-G-C

44276634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45855639-G-T

44276659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45855611-G-A

44276659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45855611-G-T

http://identifiers.org/hco/6/GRCh38#44276767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#45855501-C-A

http://identifiers.org/hco/6/GRCh38#44276775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#45855493-C-A

44276775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45855493-C-T

44276893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45855357-T-C

44276893-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45855357-T-G

44276938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45855327-G-A

44276938-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45855327-G-C

http://identifiers.org/hco/6/GRCh38#44276963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#45855305-C-A

44276963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45855305-C-T

http://identifiers.org/hco/6/GRCh38#44276967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#45855301-C-A

44276967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45855301-C-T

44276980-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45855293-T-A

44276980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45855293-T-C

44277031-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45855237-T-G

44277042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45855227-G-A

44277042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45855227-G-T

http://identifiers.org/hco/6/GRCh38#44277060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#45855209-C-A

44277060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45855209-C-T

44277075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45855196-A-G

44277337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45854941-T-C

44277455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45854820-G-T

44277505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45854789-A-G

44277590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45854709-G-T

44277598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45854702-G-A

44277598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45854702-G-T

http://identifiers.org/hco/6/GRCh38#44277602-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#45854698-A-C

44277602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45854698-A-G

44277604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45854696-T-C

44277607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45854693-G-A

44277607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45854693-G-T

44277703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45854592-T-C

http://identifiers.org/hco/6/GRCh38#44277738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#45854566-C-A

44277738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45854566-C-T

44277782-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45854535-G-C

44277831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45854486-A-G

44277868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45854458-A-G

http://identifiers.org/hco/6/GRCh38#44277871-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#45854455-A-C

44277871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45854455-A-G

44278113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45854252-G-A

44278113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45854252-G-T

44278190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45854173-G-A

44278206-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45854158-T-G

44278226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45854138-A-G

44278261-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45854102-G-T

http://identifiers.org/hco/6/GRCh38#44278339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#45854024-C-A

http://identifiers.org/hco/6/GRCh38#44278394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#45853969-C-A

44278398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45853965-G-A

44278398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45853965-G-T

44278498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45853855-C-T

44278503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45853850-G-A

44278503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45853850-G-T

44278652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45853697-G-T

http://identifiers.org/hco/6/GRCh38#44279075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#45853227-C-A

44279075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45853227-C-T

44279138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45853180-G-A

44279216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45853106-G-A

44279216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45853106-G-T

44279227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45853095-G-T

44279230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45853092-G-A

44279230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45853092-G-T

http://identifiers.org/hco/6/GRCh38#44279322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#45853001-C-A

44279322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 45853001-C-T

44279336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45852987-G-A

44279336-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45852987-G-T

44279553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45852836-T-C

44279637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 45852799-G-A

44279638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 45852798-G-A

44279701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45852751-G-A

44279701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45852751-G-T

http://identifiers.org/hco/6/GRCh38#44279742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#45852702-C-A

44279742-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45852702-C-G

44279771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45852665-G-A

44279779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45852657-G-A

http://identifiers.org/hco/6/GRCh38#44279855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#45852566-C-A

44279855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45852566-C-T

http://identifiers.org/hco/6/GRCh38#44279895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#45852526-C-A

44279895-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45852526-C-G

44279895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45852526-C-T

44279977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45852463-G-T

44279986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45852462-C-T

http://identifiers.org/hco/6/GRCh38#44280017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#45852437-C-A

http://identifiers.org/hco/6/GRCh38#44280038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#45852415-C-A

44280038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45852415-C-T

44280164-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45852298-A-T

44280186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, missense_variant
orthologous variants: 45852276-C-T

44280275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, missense_variant
orthologous variants: 45852172-T-C

http://identifiers.org/hco/6/GRCh38#44280457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#45851999-C-A

http://identifiers.org/hco/6/GRCh38#44280502-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#45851964-A-C

44280502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45851964-A-G

44280502-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45851964-A-T

44280510-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45851956-T-A

44280510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45851956-T-C

44280510-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45851956-T-G

44282088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45851036-A-G

44282143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 45850980-G-A

44282225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, missense_variant
orthologous variants: 45850898-G-A

44282225-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, missense_variant
orthologous variants: 45850898-G-C

44282580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45850543-T-C

44282584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45850539-G-A

44282584-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45850539-G-C

44282607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45850520-A-G

44282612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45850515-G-T

http://identifiers.org/hco/6/GRCh38#44282616-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#45850510-A-C

44282616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45850510-A-G

44282652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45850477-G-T

44282743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45850394-T-C

http://identifiers.org/hco/6/GRCh38#44285880-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#45846330-C-A

44285880-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: 45846330-C-G

44285880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: 45846330-C-T

44285939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45846260-G-T

44285945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45846254-G-T

44286012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 45846187-A-G

44286012-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 45846187-A-T

44286169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, missense_variant
orthologous variants: 45846030-G-A

44286169-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, stop_gained
orthologous variants: 45846030-G-C

44286232-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, missense_variant
orthologous variants: 45845967-A-T

44286479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, missense_variant
orthologous variants: 45845720-G-A

http://identifiers.org/hco/6/GRCh38#44286584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#45845621-C-A

http://identifiers.org/hco/6/GRCh38#44286597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#45845608-C-A

44286597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45845608-C-T

44286598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45845607-A-G

44286598-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45845607-A-T

http://identifiers.org/hco/6/GRCh38#44286641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#45845578-C-A

44286641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45845578-C-T

44286781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45845334-A-G

44286846-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45845234-C-G

44286924-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45845157-G-C

44287211-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 45844747-G-C

44287413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45844460-G-A

44287413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45844460-G-T

44287433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45844423-G-T

44287441-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45844415-G-C

44287441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45844415-G-T

44287446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45844403-T-C

44287454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45844395-G-A

44287454-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45844395-G-C

44287454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45844395-G-T

44287539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45844303-A-G

44287539-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45844303-A-T

44287836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 45844013-G-A

44287852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 45843997-G-A

44287904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 45843944-G-A

44287904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 45843944-G-T

44287939-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45843904-T-G

44287984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45843877-G-A

44287984-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45843877-G-C

44287987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45843874-G-T

44288042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45843803-T-C

44288042-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45843803-T-G

http://identifiers.org/hco/6/GRCh38#44288068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#45843782-C-A

44288068-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45843782-C-G

44288259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45843610-A-G

44288389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45843500-G-A

44288395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45843494-C-T

http://identifiers.org/hco/6/GRCh38#44289777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#45841495-C-A

44290851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45840771-G-A

http://identifiers.org/hco/6/GRCh38#44291148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#45840544-C-A

44291808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45838328-G-A

44291808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45838328-G-T

http://identifiers.org/hco/6/GRCh38#44291972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#45838200-C-A

44291987-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45838185-G-C

44292061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45838124-C-T

44292103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45838083-T-C

44292177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45838003-C-T

44292187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45837993-C-T

44292194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45837988-T-C

44292216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45837967-A-G

44292297-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45837891-G-C

44292671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 45837606-T-C

44295159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45836596-G-A

http://identifiers.org/hco/6/GRCh38#44295415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#45836340-C-A

44295547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45836242-G-A

44295719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45836080-G-A

44295720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45836079-C-T

44295834-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45835984-T-G

44295868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45835950-T-C

44295950-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45835867-T-G

44296159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45835698-T-C

44296166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45835687-C-T

44296383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 45835536-G-A

http://identifiers.org/hco/6/GRCh38#44296458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#45835448-C-A

44296739-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45835247-C-G

44296799-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45835183-G-C

44296949-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45835023-G-C

44297178-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 45834883-T-A

http://identifiers.org/hco/6/GRCh38#44297227-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#45834852-A-C

44297402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 45834750-G-A

44297402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 45834750-G-T

44297514-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 45834629-A-T

44297592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 45834555-C-T

44297619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 45834534-G-T

44297630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 45834523-G-A

44297630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 45834523-G-T

http://identifiers.org/hco/6/GRCh38#44297640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#45834514-C-A

44297640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 45834514-C-T

44297675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 45834479-G-A

44297675-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 45834479-G-C

44297706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: 45834451-G-A

44297801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: 45834392-G-A

44297801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: 45834392-G-T

44297822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: 45834376-T-C

44298078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45834178-T-C

44298175-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45834091-C-G

44298328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45833995-G-A

44298328-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45833995-G-C

44298366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45833956-G-T

44298523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45833809-G-A

44298589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45833744-C-T

44298632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45833711-T-C

44298965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45832905-A-G

44300387-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45831533-T-A

http://identifiers.org/hco/6/GRCh38#44300411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#45831513-C-A

44300411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45831513-C-T

44300416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45831508-T-C

44300416-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45831508-T-G

44300441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45831483-G-A

44300441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45831483-G-T

44300536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45831384-G-A

44300538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45831382-G-A

44300538-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45831382-G-C

44300542-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45831378-C-G

44300602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 45831319-G-A

44300602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 45831319-G-T

http://identifiers.org/hco/6/GRCh38#44300626-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#45831295-A-C

44300632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 45831289-C-T

http://identifiers.org/hco/6/GRCh38#44300662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#45831259-C-A

44300689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 45831232-G-A

44300689-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 45831232-G-C

44300738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: 45831173-G-A

44300738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: 45831173-G-T

http://identifiers.org/hco/6/GRCh38#44300755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#45831156-C-A

44300755-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: 45831156-C-G

44300794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: 45831117-T-C

http://identifiers.org/hco/6/GRCh38#44300801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#45831110-C-A

http://identifiers.org/hco/6/GRCh38#44300816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#45831095-C-A

44300816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: 45831095-C-T

44300825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: 45831086-G-T

44300835-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: 45831076-G-C

44300835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: 45831076-G-T

http://identifiers.org/hco/6/GRCh38#44300842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#45831067-C-A

44300842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: 45831067-C-T

44300847-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: 45831060-G-C

44300847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: 45831060-G-T

44300862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: 45830998-G-A

44300878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: 45830982-T-C

http://identifiers.org/hco/6/GRCh38#44300910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#45830959-C-A

44300910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: 45830959-C-T

44300930-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: 45830939-T-A

http://identifiers.org/hco/6/GRCh38#44300964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#45830909-C-A

44300982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: 45830891-G-A

44300982-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: 45830891-G-C

44300982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: 45830891-G-T

44300986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: 45830886-A-G

44301012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: 45830856-T-C

44301012-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: 45830856-T-G

http://identifiers.org/hco/6/GRCh38#44301026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#45830842-C-A

44301083-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: 45830795-A-T

44301314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: 45830584-A-G

44301314-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: 45830584-A-T

http://identifiers.org/hco/6/GRCh38#44301420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#45830481-C-A

44301420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 45830481-C-T

http://identifiers.org/hco/6/GRCh38#44301495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#45830398-C-A

44301495-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45830398-C-G

44301495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45830398-C-T

44301606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45830307-G-A

44301888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45830033-A-G

http://identifiers.org/hco/6/GRCh38#44301948-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#45829992-A-C

44301948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45829992-A-G

44302072-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 45829877-C-G

44302186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45829764-G-A

44302235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45829736-A-G

44302315-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45829668-A-T

44302316-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45829667-G-C

44302341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45829642-G-A

44302341-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45829642-G-C

44302359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45829624-G-A

44302380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45829596-G-A

44302392-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 45829583-T-A

44302444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, missense_variant
orthologous variants: 45829531-G-A

44302444-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, missense_variant
orthologous variants: 45829531-G-C

44302464-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, missense_variant
orthologous variants: 45829511-T-A

http://identifiers.org/hco/6/GRCh38#44302500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#45829475-C-A

http://identifiers.org/hco/6/GRCh38#44302522-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#45829454-A-C

44302583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45829393-T-C

http://identifiers.org/hco/6/GRCh38#44302641-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#45829331-A-C

http://identifiers.org/hco/6/GRCh38#44302719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#45829275-C-A

44302719-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45829275-C-G

44302750-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45829246-T-G

44302881-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, missense_variant
orthologous variants: 45829103-T-G

44302934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45829067-A-G

44302959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45829044-G-A

44302967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45829036-C-T

44303018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45828991-G-T

44303102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, missense_variant
orthologous variants: 45828909-G-A

44303184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45828827-A-G

44303274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45828766-T-C

44303277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45828763-C-T

44303417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 45828623-A-G

44303417-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, missense_variant
orthologous variants: 45828623-A-T

44304103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45828473-G-A

44304103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron variant
orthologous variants: 45828473-G-T

44304185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, missense_variant
orthologous variants: 45828373-G-A

http://identifiers.org/hco/6/GRCh38#44304327-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#45828231-A-C

44304410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: 45828149-G-A

44304445-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 45828114-T-A

44304462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 45828097-C-T

44304510-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 45828049-C-G

44304511-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 45828048-C-G

44304511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 45828048-C-T

44304557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: 45827996-T-C

44304623-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: 45827936-C-G

44304715-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 45827847-C-G

44304759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 45827803-C-T

44304763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 45827799-G-A

44304845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: 45827717-G-A

44304980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: 45827592-G-A

44305025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: 45827550-T-C

44305029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: 45827546-G-A

44305036-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: 45827539-C-G

44305037-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: 45827538-T-G

44305182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 45827393-G-A

44305205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 45827370-G-A

44305213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: 45827362-T-C

44305214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: 45827354-G-A

44305214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: 45827354-G-T

44305609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: 45827040-G-A

44305783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 45826872-T-C

44305876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: 45826777-G-A

44305876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: 45826777-G-T

44305943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: 45826740-A-G

44306138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: 45826574-G-T

http://identifiers.org/hco/6/GRCh38#44306148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#45826564-C-A

44306148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: 45826564-C-T

44306157-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: 45826555-A-T

44306169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: 45826541-G-A

44306195-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: 45826518-A-T

44306204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: 45826509-G-A

44306204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: 45826509-G-T

http://identifiers.org/hco/6/GRCh38#44306336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#45826379-C-A

44306336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 45826379-C-T

http://identifiers.org/hco/6/GRCh38#44306396-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#45826319-A-C

44306434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: 45826277-G-A

44306434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: 45826277-G-T

44306458-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: 45826242-C-G

44306458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: 45826242-C-T

44306460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: 45826240-A-G

44306461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: 45826239-T-C

44306495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, missense_variant, splice_region_variant, undefined
orthologous variants: 45826206-T-C

44306545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: 45826156-G-A

44306595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: 45826121-C-T

44306617-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: 45826104-C-G

http://identifiers.org/hco/6/GRCh38#44306776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#45825938-C-A

44306783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: 45825931-A-G

44306894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: intron_variant, undefined
orthologous variants: 45825846-C-T

44307052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 45825688-G-A

44307060-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 45825680-T-A

44307060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 45825680-T-C

44307060-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 45825680-T-G

44307399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant, splice_region_variant, undefined
orthologous variants: 45825411-G-A

44307399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant, splice_region_variant, undefined
orthologous variants: 45825411-G-T

44307421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 45825384-G-A

44307421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21315
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 45825384-G-T