http://identifiers.org/hco/10/GRCh38#27673118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#6934741-C-A

27673118-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 3 prime UTR variant
orthologous variants: 6934741-C-G

27673174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 3 prime UTR variant
orthologous variants: 6934791-T-C

http://identifiers.org/hco/10/GRCh38#27673541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#6935128-C-A

27673624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 3 prime UTR variant
orthologous variants: 6935211-T-C

27673840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 3 prime UTR variant
orthologous variants: 6935425-G-A

http://identifiers.org/hco/10/GRCh38#27673858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#6935443-C-A

27673858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 3 prime UTR variant
orthologous variants: 6935443-C-T

27674065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 3 prime UTR variant
orthologous variants: 6935671-T-C

http://identifiers.org/hco/10/GRCh38#27674156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#6935764-C-A

27674156-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 3 prime UTR variant
orthologous variants: 6935764-C-G

27674193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 3 prime UTR variant
orthologous variants: 6935820-A-G

27674443-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 3 prime UTR variant
orthologous variants: 6936077-G-C

27674638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 3 prime UTR variant
orthologous variants: 6936254-T-C

27674726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 3 prime UTR variant
orthologous variants: 6936375-T-C

27674726-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 3 prime UTR variant
orthologous variants: 6936375-T-G

http://identifiers.org/hco/10/GRCh38#27674738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#6936382-C-A

27674738-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 3 prime UTR variant
orthologous variants: 6936382-C-G

27674738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 3 prime UTR variant
orthologous variants: 6936382-C-T

http://identifiers.org/hco/10/GRCh38#27674743-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#6936387-A-C

27674745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 3 prime UTR variant
orthologous variants: 6936389-G-A

27674745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 3 prime UTR variant
orthologous variants: 6936389-G-T

http://identifiers.org/hco/10/GRCh38#27674750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#6936394-C-A

27674750-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 3 prime UTR variant
orthologous variants: 6936394-C-G

27674750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 3 prime UTR variant
orthologous variants: 6936394-C-T

27674839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 3 prime UTR variant
orthologous variants: 6936491-G-A

27674839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 3 prime UTR variant
orthologous variants: 6936491-G-T

27674845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 3 prime UTR variant
orthologous variants: 6936495-G-A

27674953-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 3 prime UTR variant
orthologous variants: 6936586-A-T

http://identifiers.org/hco/10/GRCh38#27674985-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#6936617-A-C

27674985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 3 prime UTR variant
orthologous variants: 6936617-A-G

27675107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 3 prime UTR variant
orthologous variants: 6936736-G-T

http://identifiers.org/hco/10/GRCh38#27675243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#6936879-C-A

27675443-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6937089-C-G

27675443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6937089-C-T

http://identifiers.org/hco/10/GRCh38#27675496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#6937142-C-A

27675496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6937142-C-T

27675541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: synonymous variant
orthologous variants: 6937188-G-A

27675589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6937236-G-A

27676828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6937830-C-T

http://identifiers.org/hco/10/GRCh38#27676963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#6937943-C-A

27676963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6937943-C-T

27677249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6938235-A-G

27677529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6938504-G-A

27677531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6938506-A-G

27677545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6938520-G-A

27677731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6938672-G-A

27677736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6938677-G-A

http://identifiers.org/hco/10/GRCh38#27677800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#6938727-C-A

27677819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6938746-C-T

27678094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6939621-A-G

27678140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6939666-T-C

27678148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6939674-G-A

27678148-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6939674-G-C

27678149-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6939675-C-G

27678149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6939675-C-T

27678328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6939885-C-T

27678516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6940056-T-C

27679690-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6941233-A-T

http://identifiers.org/hco/10/GRCh38#27679899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#6941427-C-A

27680180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6941649-G-A

27680222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6941689-C-T

27680523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6941982-T-C

27683589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6942198-C-T

27683855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6942410-G-A

27684357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6942718-C-T

27685314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6944118-C-T

27685735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6944211-C-T

27685798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6944281-C-T

27686183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6944642-G-A

27686183-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6944642-G-C

27687526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6945318-C-T

27687565-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6945343-C-G

27687660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6945454-G-A

27687660-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6945454-G-C

27687975-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6945747-G-C

27688147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6945881-A-G

27688243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6945960-C-T

27688902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6946577-C-T

27689312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6946997-C-T

27689379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6947060-G-A

27689421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6947102-G-A

27689456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6947137-T-C

27689586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6947542-T-C

27689849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6947799-A-G

27689873-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6947847-A-T

27689923-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6947896-T-G

27689935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6947903-G-A

27689935-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6947903-G-C

27689938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6947906-T-C

27689984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6947952-A-G

27690002-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6947970-G-C

27690094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6948248-C-T

27690102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6948256-G-A

27690484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6948551-G-T

27690678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6948746-C-T

27690789-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6948853-C-G

http://identifiers.org/hco/10/GRCh38#27690797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#6948861-C-A

27691424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6949115-T-C

27692284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6949383-A-G

27692297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6949396-T-C

27694779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6952174-A-G

27694798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6952193-G-A

27694798-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6952193-G-C

27694830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6952224-T-C

27695046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6952454-G-A

27695214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6952610-A-G

http://identifiers.org/hco/10/GRCh38#27695272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#6952669-C-A

27695454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6952841-T-C

27695454-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6952841-T-G

27695482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6952869-T-C

27695587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6952953-G-A

27696016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6954431-G-A

27696066-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6954474-T-G

http://identifiers.org/hco/10/GRCh38#27696121-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#6954542-A-C

27696723-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6955058-C-G

27696949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6955343-A-G

27697082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6955471-G-A

27697316-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6955675-A-T

27697378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6955738-G-A

27697509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6955950-T-C

27697723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6956145-C-T

27698202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6956519-G-T

27698382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6956679-A-G

27698394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6956691-G-A

27698435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6956728-G-T

27698439-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6956732-G-C

27698460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6956752-C-T

27698629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6956892-A-G

27698835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6957066-G-A

27698865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6957090-T-C

27698865-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6957090-T-G

27700158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6958111-G-A

27700158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6958111-G-T

27701018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6959080-G-A

27702376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6959845-G-T

27702498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6959951-C-T

27702645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6960079-T-C

27702935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6960380-A-G

http://identifiers.org/hco/10/GRCh38#27702963-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#6960417-A-C

27703350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6960784-A-G

27712046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6967293-G-A

27713371-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6967788-C-G

27713371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6967788-C-T

27713404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6967820-A-G

27713566-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6968002-T-G

27713781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6968209-G-A

27713849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6968266-T-C

27713998-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6968410-T-G

27714041-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6968445-T-G

27714207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6968611-G-T

27714279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6968683-C-T

27714810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6969163-C-T

27714905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6969253-G-A

27715030-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6969359-T-A

http://identifiers.org/hco/10/GRCh38#27715181-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#6969589-A-C

27715216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6969624-T-C

27715528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6969917-C-T

27715866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6970196-G-A

27716219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6970555-T-C

27716222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6970558-A-G

27716379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6970624-T-C

27716646-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6970854-T-A

27716863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6971075-A-G

http://identifiers.org/hco/10/GRCh38#27716948-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#6971165-A-C

27716948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6971165-A-G

27716985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6971200-G-T

27717691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6971822-T-C

27717691-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6971822-T-G

27717712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6971834-G-A

27717738-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6971857-C-G

27717738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6971857-C-T

27717840-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6971947-G-C

27717859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6971966-A-G

27717884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6971989-A-G

27717889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6971993-T-C

27717940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6972046-G-T

27718172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6972253-C-T

27718186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6972267-A-G

27718332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 6972399-A-G

27718349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 6972416-C-T

27718373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 6972431-A-G

http://identifiers.org/hco/10/GRCh38#27718453-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#6972510-A-C

http://identifiers.org/hco/10/GRCh38#27718647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#6972697-C-A

27718647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6972697-C-T

http://identifiers.org/hco/10/GRCh38#27718663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#6972706-C-A

27718663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6972706-C-T

27718669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6972712-G-A

27718671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6972714-A-G

27718855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6972901-C-T

27718978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6974721-C-T

27719142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6974871-C-T

27719325-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6975038-T-G

http://identifiers.org/hco/10/GRCh38#27719377-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#6975091-A-C

27719391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6975105-T-C

27719477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6975180-A-G

27720208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6976011-T-C

27720284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6976085-A-G

27720545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6976319-A-G

http://identifiers.org/hco/10/GRCh38#27720555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#6976329-C-A

27720612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6976380-T-C

http://identifiers.org/hco/10/GRCh38#27720650-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#6976425-A-C

27720671-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron_variant, undefined
orthologous variants: 6976460-C-G

27720701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron_variant, undefined
orthologous variants: 6976489-G-A

27721251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6976945-G-A

27721977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6977410-T-C

http://identifiers.org/hco/10/GRCh38#27721978-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#6977411-A-C

27722212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6977605-T-C

27722238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6977632-C-T

27722325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6977691-G-A

27722372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6977739-T-C

27722433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6977799-A-G

27722547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6977912-G-A

27722790-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6978086-C-G

27722995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6978293-T-C

27723091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6978379-A-G

27723548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6978971-C-T

27723686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6979237-C-T

27723832-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6979385-G-C

27724128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6979660-A-G

27724325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6979815-G-A

27725026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6981377-G-A

27725043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6981393-G-A

27725354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6981602-C-T

27725586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6981831-A-G

http://identifiers.org/hco/10/GRCh38#27725676-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#6981933-A-C

http://identifiers.org/hco/10/GRCh38#27726034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#6982355-C-A

27726304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6982611-T-C

27726797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6983076-G-T

27727719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6984421-G-A

27727853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6984657-A-G

27727894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6984698-T-C

http://identifiers.org/hco/10/GRCh38#27727905-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#6984709-A-C

27727983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6984782-G-A

27728241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6985093-G-A

27728249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6985101-A-G

27728272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6985122-G-A

http://identifiers.org/hco/10/GRCh38#27728294-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#6985142-A-C

http://identifiers.org/hco/10/GRCh38#27728324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#6985158-C-A

27728324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6985158-C-T

27728748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6985490-G-A

27728883-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6985614-C-G

27728921-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6985642-C-G

27729068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6985755-C-T

27729123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6985803-T-C

27729241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6985909-A-G

http://identifiers.org/hco/10/GRCh38#27729255-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#6985918-A-C

27729861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6986337-G-A

27729917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6986390-G-A

27729996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6986448-T-C

27730044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6986501-C-T

27731289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6987148-A-G

27731407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6987253-C-T

27731445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6987289-G-A

27731445-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6987289-G-C

27731487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6987340-A-G

27731585-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6987443-T-G

27731995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6987823-T-C

27732101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6987927-T-C

27732198-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6988010-C-G

27732283-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6988314-T-A

27733696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6991072-C-T

27733725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6991104-T-C

27733729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6991108-G-T

27733750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6991127-G-A

27733772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6991149-C-T

27733909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6991275-A-G

27733917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6991283-C-T

27733933-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6991299-T-A

27733933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6991299-T-C

27733984-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6991351-T-G

27734369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6991955-T-C

http://identifiers.org/hco/10/GRCh38#27734386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#6991972-C-A

27734410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6991996-C-T

http://identifiers.org/hco/10/GRCh38#27734667-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#6992249-A-C

27734667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: synonymous variant
orthologous variants: 6992249-A-G

27734688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: synonymous variant
orthologous variants: 6992270-C-T

27734704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: missense variant
orthologous variants: 6992286-A-G

27734706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: synonymous variant
orthologous variants: 6992288-C-T

27734748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: synonymous variant
orthologous variants: 6992330-A-G

27734754-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: synonymous variant
orthologous variants: 6992336-C-G

27734867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6992447-T-C

27734894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6992476-A-G

27734910-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6992492-T-A

27734910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6992492-T-C

27734910-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6992492-T-G

27735136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6992698-G-A

27735136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6992698-G-T

27735168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6992726-G-T

http://identifiers.org/hco/10/GRCh38#27735239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#6992799-C-A

27735239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: missense variant
orthologous variants: 6992799-C-T

27735381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 6992941-C-T

27735427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6992983-G-A

27735427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6992983-G-T

27735933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6994647-C-T

27735999-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6994699-T-A

27736292-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6994986-C-G

27736471-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6995175-T-G

27736480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6995184-C-T

27736629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6995297-G-A

27736696-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6995405-C-G

27737745-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6995723-T-G

27737805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6995787-T-C

27737811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6995793-C-T

27738213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6996324-G-T

27738400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6996503-C-T

27738402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6996505-A-G

27738699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6996674-A-G

27738898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6996923-G-T

27739233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6997210-A-G

27739324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6998434-G-A

27739371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6998483-A-G

http://identifiers.org/hco/10/GRCh38#27739487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#6998593-C-A

27740428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6999680-T-C

27740667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 6999896-C-T

27740876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 7000038-C-T

27741013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 7000163-C-T

27741014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 7000164-C-T

27741063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 7000217-C-T

http://identifiers.org/hco/10/GRCh38#27741172-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7000389-C-A

27741193-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 7000410-T-G

27741282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron_variant, undefined
orthologous variants: 7000535-A-G

http://identifiers.org/hco/10/GRCh38#27741294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7000547-C-A

27741294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 7000547-C-T

http://identifiers.org/hco/10/GRCh38#27741405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7000653-C-A

27741405-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: synonymous variant
orthologous variants: 7000653-C-G

27741480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: synonymous variant
orthologous variants: 7000728-C-T

27741511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 7000759-C-T

27741519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 7000767-G-T

27741609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 7000863-C-T

27741614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 7000868-T-C

27741650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 7000950-G-A

27741650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 7000950-G-T

27741805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 7001155-C-T

27741934-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 7001248-G-C

27741988-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 7001297-G-T

27742105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 7001393-C-T

27742131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 7001421-C-T

http://identifiers.org/hco/10/GRCh38#27742462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#7001737-C-A

27742558-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron_variant, undefined
orthologous variants: 7001807-G-C

27742640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 7001886-C-T

27742821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 7002044-G-T

http://identifiers.org/hco/10/GRCh38#27743173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7002307-C-A

27743173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 7002307-C-T

http://identifiers.org/hco/10/GRCh38#27743195-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7002330-A-C

27743195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 7002330-A-G

27743195-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 7002330-A-T

27743213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 7002342-G-A

27743213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 7002342-G-T

27743329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: synonymous variant
orthologous variants: 7002458-G-A

27743329-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: synonymous variant
orthologous variants: 7002458-G-C

27743329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: synonymous variant
orthologous variants: 7002458-G-T

27743331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: missense variant
orthologous variants: 7002460-G-A

http://identifiers.org/hco/10/GRCh38#27743468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7002594-C-A

27743468-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 5 prime UTR variant
orthologous variants: 7002594-C-G

27743468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 5 prime UTR variant
orthologous variants: 7002594-C-T

27743477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 5 prime UTR variant
orthologous variants: 7002603-C-T

http://identifiers.org/hco/10/GRCh38#27743480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7002606-C-A

27743480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 5 prime UTR variant
orthologous variants: 7002606-C-T

27743493-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 5_prime_UTR_variant, splice_region_variant
orthologous variants: 7002619-G-C

27743504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant
orthologous variants: 7002630-G-T

27743659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 7002784-C-T

27743692-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 7002812-T-G

27743795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 7002897-C-T

27744097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 7003188-G-A

27744097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 7003188-G-T

http://identifiers.org/hco/10/GRCh38#27744103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7003194-C-A

27744111-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 7003200-G-C

27744117-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 7003206-G-C

27744169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 7003272-C-T

http://identifiers.org/hco/10/GRCh38#27744249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7003323-C-A

27744249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 7003323-C-T

27744250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 7003324-C-T

27744343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 7003367-G-A

27744355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 7003379-A-G

27744355-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 7003379-A-T

http://identifiers.org/hco/10/GRCh38#27744427-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7003417-A-C

27744427-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron variant
orthologous variants: 7003417-A-T

27744551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 7003546-C-T

27744649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 7003630-G-A

27744649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 7003630-G-T

http://identifiers.org/hco/10/GRCh38#27744689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#7003642-C-A

http://identifiers.org/hco/10/GRCh38#27744697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#7003650-C-A

27744697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron_variant, undefined
orthologous variants: 7003650-C-T

http://identifiers.org/hco/10/GRCh38#27744741-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#7003694-C-A

27744741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron_variant, undefined
orthologous variants: 7003694-C-T

http://identifiers.org/hco/10/GRCh38#27744743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#7003696-C-A

27744743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron_variant, undefined
orthologous variants: 7003696-C-T

http://identifiers.org/hco/10/GRCh38#27744745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#7003698-C-A

27744745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron_variant, undefined
orthologous variants: 7003698-C-T

http://identifiers.org/hco/10/GRCh38#27744747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#7003700-C-A

http://identifiers.org/hco/10/GRCh38#27744758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#7003755-C-A

27744758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron_variant, undefined
orthologous variants: 7003755-C-T

27744779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron_variant, undefined
orthologous variants: 7003783-G-A

27744779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron_variant, undefined
orthologous variants: 7003783-G-T

http://identifiers.org/hco/10/GRCh38#27744860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#7003862-C-A

27744860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron_variant, undefined
orthologous variants: 7003862-C-T

http://identifiers.org/hco/10/GRCh38#27744911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#7003914-C-A

27744911-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 7003914-C-G

27744911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 7003914-C-T

27744941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 7003942-G-A

27744953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 7003954-G-A

27744953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 7003954-G-T

http://identifiers.org/hco/10/GRCh38#27744957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#7003958-C-A

27745007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 7004008-C-T

27745326-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 7004236-T-A

27745326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 7004236-T-C

27745441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 7004369-G-A

27745441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 7004369-G-T

http://identifiers.org/hco/10/GRCh38#27745454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#7004382-C-A

http://identifiers.org/hco/10/GRCh38#27745542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#7004455-C-A

27745542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 7004455-C-T

27745582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 7004496-T-C

27745599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron_variant, undefined
orthologous variants: 7004517-G-A

27745599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron_variant, undefined
orthologous variants: 7004517-G-T

27745646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron_variant, undefined
orthologous variants: 7004566-G-A

http://identifiers.org/hco/10/GRCh38#27745690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#7004600-C-A

27745690-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron_variant, undefined
orthologous variants: 7004600-C-G

27745690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron_variant, undefined
orthologous variants: 7004600-C-T

http://identifiers.org/hco/10/GRCh38#27745701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#7004616-C-A

27745701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: intron_variant, undefined
orthologous variants: 7004616-C-T

27745761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 7004668-G-T

27745799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 7004706-G-A

27745799-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 7004706-G-C

27745799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 7004706-G-T

27745840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 7004747-G-A

27745840-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 7004747-G-C

27745840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 7004747-G-T

27745926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 7004833-G-A

27745964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 7004871-G-A

27745964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23729
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 7004871-G-T