34579504-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 5 prime UTR variant
orthologous variants: 82278304-C-G

34579504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 5 prime UTR variant
orthologous variants: 82278304-C-T

http://identifiers.org/hco/17/GRCh38#34579580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82278387-C-A

34579580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 5 prime UTR variant
orthologous variants: 82278387-C-T

34579592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 5 prime UTR variant
orthologous variants: 82278399-G-A

34579592-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 5 prime UTR variant
orthologous variants: 82278399-G-C

http://identifiers.org/hco/17/GRCh38#34579696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82278483-C-A

34579696-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 5 prime UTR variant
orthologous variants: 82278483-C-G

http://identifiers.org/hco/17/GRCh38#34579741-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82278528-C-A

http://identifiers.org/hco/17/GRCh38#34579755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82278543-C-A

34580026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 5 prime UTR variant
orthologous variants: 82278817-G-A

34580026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 5 prime UTR variant
orthologous variants: 82278817-G-T

34580055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 5 prime UTR variant
orthologous variants: 82278850-G-A

34580055-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 5 prime UTR variant
orthologous variants: 82278850-G-C

34580055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 5 prime UTR variant
orthologous variants: 82278850-G-T

34580093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 5 prime UTR variant
orthologous variants: 82278888-G-A

34580093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 5 prime UTR variant
orthologous variants: 82278888-G-T

http://identifiers.org/hco/17/GRCh38#34580144-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82278952-A-C

34580144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 5 prime UTR variant
orthologous variants: 82278952-A-G

34580144-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 5 prime UTR variant
orthologous variants: 82278952-A-T

http://identifiers.org/hco/17/GRCh38#34580146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82278954-C-A

34580146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 5 prime UTR variant
orthologous variants: 82278954-C-T

http://identifiers.org/hco/17/GRCh38#34580325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82279133-C-A

34580471-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 5 prime UTR variant
orthologous variants: 82279276-C-G

34580521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 5 prime UTR variant
orthologous variants: 82279326-G-T

http://identifiers.org/hco/17/GRCh38#34580543-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82279346-A-C

34580619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 82279422-G-A

34580619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 82279422-G-T

34580718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 82279521-G-A

34580743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 5 prime UTR variant
orthologous variants: 82279546-A-G

34580901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 5 prime UTR variant
orthologous variants: 82279705-G-A

34580901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 5 prime UTR variant
orthologous variants: 82279705-G-T

http://identifiers.org/hco/17/GRCh38#34580923-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82279726-A-C

34580923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 5 prime UTR variant
orthologous variants: 82279726-A-G

34580923-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 5 prime UTR variant
orthologous variants: 82279726-A-T

http://identifiers.org/hco/17/GRCh38#34580970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82279774-C-A

34580970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 5 prime UTR variant
orthologous variants: 82279774-C-T

34581030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 5 prime UTR variant
orthologous variants: 82279826-G-A

34581030-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 5 prime UTR variant
orthologous variants: 82279826-G-C

34581030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 5 prime UTR variant
orthologous variants: 82279826-G-T

34581161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82279957-G-T

34581223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82280019-G-A

34581223-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82280019-G-C

34581223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82280019-G-T

34581247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82280051-G-A

34581247-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82280051-G-C

http://identifiers.org/hco/17/GRCh38#34581249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82280053-C-A

34581249-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82280053-C-G

34581249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82280053-C-T

http://identifiers.org/hco/17/GRCh38#34581269-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82280071-C-A

34581582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82280346-G-T

34581586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82280350-G-T

34581621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82280385-C-T

34581926-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82280666-G-T

34581945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82280685-G-T

34582042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82280788-T-C

34582165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82280914-G-A

34582165-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82280914-G-C

34582215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82280964-G-A

34582306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82281049-C-T

http://identifiers.org/hco/17/GRCh38#34582589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82281352-C-A

34582600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82281362-G-A

34582600-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82281362-G-C

34582600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82281362-G-T

34582661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82281414-C-T

34582699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82281455-G-A

34582961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82281620-G-A

34583038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82281697-C-T

http://identifiers.org/hco/17/GRCh38#34583345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82281943-C-A

34583345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82281943-C-T

34583503-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82282068-C-G

34583654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82282214-C-T

34583903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82282473-G-A

34584073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82282640-T-C

34584143-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82282703-G-C

34584509-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82282981-A-T

34584521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82282990-G-A

34584816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82283193-G-A

34584819-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82283196-G-C

34585253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82283459-T-C

http://identifiers.org/hco/17/GRCh38#34585425-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82283575-A-C

34585840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82283950-A-G

34585906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82284011-A-G

34586046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82284264-C-T

34586112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82284389-G-A

34586112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82284389-G-T

34586119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82284395-C-T

34586131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82284407-C-T

http://identifiers.org/hco/17/GRCh38#34586165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82284444-C-A

34586165-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82284444-C-G

34586165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82284444-C-T

http://identifiers.org/hco/17/GRCh38#34586176-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82284455-A-C

34586187-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82284467-C-G

34586187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82284467-C-T

34586425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82284705-G-A

34586585-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82284838-T-A

http://identifiers.org/hco/17/GRCh38#34586848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82285172-C-A

34586900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82285238-T-C

34587006-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82285345-A-T

34589895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82287716-A-G

34590011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82287829-G-A

http://identifiers.org/hco/17/GRCh38#34590130-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82287923-A-C

34590243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82288012-A-G

34590257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82288022-C-T

34590332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82288099-C-T

34590496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82288557-C-T

34590664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82288706-G-A

34590762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82288824-A-G

34590867-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82288929-T-A

34591989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82289490-C-T

34592017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82289515-T-C

34592049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82289555-A-G

34592206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82289711-C-T

34592223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82289728-C-T

34592316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82289780-G-A

34592316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82289780-G-T

34592385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82289860-C-T

34592707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82290098-C-T

34592773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82290152-G-T

34592849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82290241-C-T

34592969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82290339-G-A

34593542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82290694-C-T

34593736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82290864-C-T

34594041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82291114-T-C

34594505-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82291583-T-A

34594939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82291724-G-A

34594970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82291748-T-C

34596754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82292376-G-A

34596819-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82292434-C-G

34596826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82292441-G-A

34596826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82292441-G-T

34596848-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82292463-T-A

34596848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82292463-T-C

34596848-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82292463-T-G

34597202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82292759-G-T

34597261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82292811-G-A

34597856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82293556-G-A

http://identifiers.org/hco/17/GRCh38#34598524-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82294075-A-C

34598537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82294088-A-G

34598560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82294109-G-A

34599394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82294905-G-A

34599394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82294905-G-T

34600865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82296782-G-A

34601562-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82297285-G-C

34601630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82297352-G-A

34601829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82297549-C-T

34601866-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82297582-C-G

34601981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82297683-A-G

34602006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82297705-C-T

34602333-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82297974-A-T

34602400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82298052-T-C

34602430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82298080-C-T

34602481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82298130-G-A

34602584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82298208-T-C

http://identifiers.org/hco/17/GRCh38#34602767-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82298370-A-C

34603185-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82298733-A-T

34603289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82298828-G-A

34603514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82299035-G-A

http://identifiers.org/hco/17/GRCh38#34603550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82299070-C-A

34603672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82299188-G-T

34603776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82299292-C-T

34604624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82300819-C-T

34604875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82301069-T-C

34604875-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82301069-T-G

34605277-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82301437-T-A

34605647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82301703-C-T

34605722-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82301779-C-G

34605722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82301779-C-T

34605727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82301784-G-A

34608256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82305310-A-G

34608522-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82305508-A-T

34608559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82305541-T-C

34608823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82305877-A-G

34608880-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82305933-T-G

34608945-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82305995-T-G

34608979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82306034-G-A

34609036-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82306090-T-A

34609224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82306137-C-T

34609497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82306353-C-T

34609620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82306438-A-G

34609860-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82306663-T-G

34609876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82306678-T-C

34609921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82306725-T-C

http://identifiers.org/hco/17/GRCh38#34610271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82306996-C-A

34610428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82307129-G-A

34611227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82307325-G-T

34611232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82307330-G-A

34611246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82307344-G-A

34611702-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82307755-C-G

34611766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82308228-G-A

34611794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82308257-G-A

http://identifiers.org/hco/17/GRCh38#34611811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82308277-C-A

34611811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82308277-C-T

34612060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82308527-C-T

34612075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82308540-A-G

http://identifiers.org/hco/17/GRCh38#34612096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82308555-C-A

34612263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82308694-G-A

34612286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82308714-C-T

34612379-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82308762-G-C

http://identifiers.org/hco/17/GRCh38#34612693-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82308972-A-C

34613224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82309448-C-T

34613467-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82309736-C-G

34613467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82309736-C-T

34613739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82310072-T-C

34613894-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82310325-C-G

http://identifiers.org/hco/17/GRCh38#34614019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82310461-C-A

34614034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82310475-T-C

34614255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82310693-A-G

http://identifiers.org/hco/17/GRCh38#34614275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82310711-C-A

http://identifiers.org/hco/17/GRCh38#34614350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82310776-C-A

http://identifiers.org/hco/17/GRCh38#34614561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82310890-C-A

34614561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82310890-C-T

34614658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82310964-T-C

http://identifiers.org/hco/17/GRCh38#34614687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82310993-C-A

34614821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82311118-A-G

34614903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82311179-A-G

34615109-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82311316-G-C

34615120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82311327-T-C

34615228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82311445-G-A

34615239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82311455-C-T

34615326-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82311489-C-G

34615326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82311489-C-T

34615559-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82311674-A-T

34615620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82311787-G-A

34615822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82312015-G-A

34615824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82312017-G-T

34615933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82312092-A-G

34616266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82312354-A-G

34616387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82312498-G-A

34616404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82312515-G-A

34616900-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82312605-C-G

34617376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82312954-T-C

34617431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82313010-A-G

34617478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82313059-G-A

34617543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82313114-C-T

34617944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82313477-C-T

34619571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82314879-T-C

http://identifiers.org/hco/17/GRCh38#34619841-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82315113-A-C

34619847-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82315119-C-G

34619847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82315119-C-T

http://identifiers.org/hco/17/GRCh38#34620102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82315331-C-A

34620102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82315331-C-T

34620259-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82315456-C-G

34620387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82315485-T-C

34620390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82315488-G-A

34620454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82315525-G-T

34620565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82315633-A-G

34620859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82315848-T-C

34621066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82316034-G-A

34621115-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82316079-C-G

34621227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82316194-G-T

34621283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82316244-G-A

34621283-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82316244-G-C

34621300-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82316260-G-C

34621362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82316308-G-T

34621392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82316355-T-C

34621578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82316513-C-T

34621579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82316514-C-T

34621770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82316664-G-T

34621776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82316670-G-A

34621781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82316675-C-T

34621865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82316780-A-G

34621865-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82316780-A-T

http://identifiers.org/hco/17/GRCh38#34621909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82316820-C-A

34621917-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82316828-C-G

34621917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82316828-C-T

34621962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82316859-T-C

http://identifiers.org/hco/17/GRCh38#34621998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82316889-C-A

34622023-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82319577-C-G

34622158-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82319705-G-C

34622194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82319740-C-T

http://identifiers.org/hco/17/GRCh38#34622214-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82319781-A-C

34622223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82319790-C-T

34622286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82319853-T-C

34622391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82319935-G-T

34622414-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82319957-G-C

34622462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82320004-G-A

34622635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82320125-C-T

34622733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82320187-G-T

34622794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82320247-T-C

34622803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82320256-G-A

34622836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82320287-A-G

http://identifiers.org/hco/17/GRCh38#34622998-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82321067-A-C

34622998-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82321067-A-T

34623033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82321103-G-A

34623215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82321265-T-C

34623247-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82321297-C-G

34623247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82321297-C-T

34623254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82321304-G-T

34623394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82321450-T-C

34623394-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82321450-T-G

http://identifiers.org/hco/17/GRCh38#34623413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82321472-C-A

34623413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82321472-C-T

34623422-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82321481-T-A

34623422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82321481-T-C

34623512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82321564-C-T

34624097-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82323308-C-G

34624128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82323339-G-A

http://identifiers.org/hco/17/GRCh38#34624137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82323349-C-A

34624139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82323351-G-A

http://identifiers.org/hco/17/GRCh38#34624171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82323378-C-A

34624335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82323543-G-A

34624439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82323647-C-T

34624581-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82323739-T-A

34624606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82323763-C-T

34624677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82323803-G-A

34624706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82323832-G-T

34624707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82323833-A-G

34624767-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82323893-T-G

34624843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82323974-T-C

http://identifiers.org/hco/17/GRCh38#34625188-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82324261-A-C

34625223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82324303-G-A

34625315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82324363-A-G

34625406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82324435-G-A

34625406-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82324435-G-C

34625460-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82324452-C-G

34625598-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82324546-C-G

34625599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82324547-A-G

http://identifiers.org/hco/17/GRCh38#34625994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82324962-C-A

34625994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82324962-C-T

34625997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82324965-G-T

http://identifiers.org/hco/17/GRCh38#34626030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82324975-C-A

34626030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82324975-C-T

34626039-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82324984-G-T

http://identifiers.org/hco/17/GRCh38#34626066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82325012-C-A

34626066-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82325012-C-G

http://identifiers.org/hco/17/GRCh38#34626257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#82325199-C-A

34626257-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: synonymous_variant, undefined
orthologous variants: 82325199-C-G

34626257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: synonymous_variant, undefined
orthologous variants: 82325199-C-T

34626365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: synonymous_variant, undefined
orthologous variants: 82325307-G-T

http://identifiers.org/hco/17/GRCh38#34626467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#82325409-C-A

34626467-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: synonymous_variant, undefined
orthologous variants: 82325409-C-G

34626467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: synonymous_variant, undefined
orthologous variants: 82325409-C-T

34626581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: synonymous variant
orthologous variants: 82325523-G-A

34626581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: synonymous variant
orthologous variants: 82325523-G-T

http://identifiers.org/hco/17/GRCh38#34626603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82325545-C-A

34626603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron_variant, missense_variant
orthologous variants: 82325545-C-T

34626662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 82325604-G-A

34626662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 82325604-G-T

34626668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 82325610-A-G

34626728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 82325670-G-A

http://identifiers.org/hco/17/GRCh38#34626730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82325672-C-A

34626730-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron_variant, missense_variant
orthologous variants: 82325672-C-G

34626730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron_variant, missense_variant
orthologous variants: 82325672-C-T

34626734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 82325676-G-T

34626801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron_variant, missense_variant
orthologous variants: 82325743-T-C

34626891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: missense variant
orthologous variants: 82325839-C-T

34626896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: synonymous variant
orthologous variants: 82325844-G-A

34626896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: synonymous variant
orthologous variants: 82325844-G-T

http://identifiers.org/hco/17/GRCh38#34626911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82325859-C-A

34626911-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: synonymous variant
orthologous variants: 82325859-C-G

34626911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: synonymous variant
orthologous variants: 82325859-C-T

34626998-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: synonymous variant
orthologous variants: 82325946-C-G

34626998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: synonymous variant
orthologous variants: 82325946-C-T

http://identifiers.org/hco/17/GRCh38#34627037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82325985-C-A

34627037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: synonymous variant
orthologous variants: 82325985-C-T

http://identifiers.org/hco/17/GRCh38#34627110-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82326054-A-C

34627297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82326385-T-C

34627401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82326488-G-A

34627516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82326584-T-C

34627516-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82326584-T-G

34627532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82326593-G-A

34627561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82326607-C-T

34627624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82326644-G-A

34627684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82326709-G-A

34627684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82326709-G-T

34627924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82326935-G-A

34627926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82326937-T-C

34627994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82327003-G-A

34627994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82327003-G-T

34628171-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82327180-T-A

34628492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82327654-A-G

34628505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82327667-A-G

http://identifiers.org/hco/17/GRCh38#34628511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82327673-C-A

34628515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82327677-G-A

34628515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82327677-G-T

34628533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82327697-C-T

http://identifiers.org/hco/17/GRCh38#34628535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82327699-C-A

34628535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82327699-C-T

34628617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: synonymous variant
orthologous variants: 82327782-G-A

34628617-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: missense variant
orthologous variants: 82327782-G-C

34628749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82327895-G-A

34628749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82327895-G-T

34628791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82327938-T-C

34628839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82327980-G-T

http://identifiers.org/hco/17/GRCh38#34629067-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82328180-A-C

34629142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: missense variant
orthologous variants: 82328255-C-T

http://identifiers.org/hco/17/GRCh38#34629258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82328373-C-A

34629258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82328373-C-T

34629265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82328380-G-A

34629265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82328380-G-T

34629308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82328430-G-A

34629308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82328430-G-T

34629309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82328431-T-C

34629341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82328448-G-A

http://identifiers.org/hco/17/GRCh38#34629343-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82328450-A-C

34629343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82328450-A-G

34629344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82328451-T-C

34629365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82328472-G-A

34629481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82328582-C-T

34629631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82328740-G-A

34629692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82328800-G-A

34629823-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82328885-G-C

34629845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82328907-G-A

34629845-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82328907-G-C

34629879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82328941-A-G

34629879-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82328941-A-T

http://identifiers.org/hco/17/GRCh38#34629935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82328991-C-A

34629935-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82328991-C-G

34629935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82328991-C-T

34629939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82328995-G-A

34629939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82328995-G-T

34629972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82329028-A-G

34629979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82329035-G-A

34629979-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82329035-G-C

http://identifiers.org/hco/17/GRCh38#34629985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82329041-C-A

34629985-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82329041-C-G

34629985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82329041-C-T

34630166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82329223-G-A

34630166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82329223-G-T

34630210-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82329240-A-T

http://identifiers.org/hco/17/GRCh38#34630213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82329251-C-A

34630213-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82329251-C-G

34630213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82329251-C-T

http://identifiers.org/hco/17/GRCh38#34630216-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82329254-A-C

34630218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82329256-A-G

34630218-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82329256-A-T

http://identifiers.org/hco/17/GRCh38#34630238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82329266-C-A

34630238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82329266-C-T

34630433-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82329433-T-A

34630447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82329447-G-A

34630522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82329508-A-G

34631853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82330596-C-T

34631875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82330620-G-A

http://identifiers.org/hco/17/GRCh38#34632217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82330972-C-A

34632217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82330972-C-T

34632218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82330973-G-A

34632557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82331128-G-A

34632557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82331128-G-T

34632561-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82331132-T-A

http://identifiers.org/hco/17/GRCh38#34633053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82331577-C-A

34633053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82331577-C-T

34633222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82331710-G-A

34633222-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82331710-G-C

34633271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82331756-G-A

http://identifiers.org/hco/17/GRCh38#34633777-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82332201-A-C

34633805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82332231-G-A

34634464-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82332991-T-G

34634671-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82333163-A-T

34634712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82333192-G-A

34634712-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82333192-G-C

34634712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82333192-G-T

34634717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82333197-A-G

http://identifiers.org/hco/17/GRCh38#34634718-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82333198-A-C

34634718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82333198-A-G

34634752-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82333231-T-A

34634752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82333231-T-C

34634762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82333241-G-T

34634763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82333242-G-A

34634763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82333242-G-T

34634770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82333249-G-T

34634883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: synonymous variant
orthologous variants: 82333372-G-A

34634922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: synonymous variant
orthologous variants: 82333411-A-G

34634937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: synonymous variant
orthologous variants: 82333426-T-C

http://identifiers.org/hco/17/GRCh38#34635121-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82333610-A-C

34635141-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82333631-C-G

34635141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82333631-C-T

http://identifiers.org/hco/17/GRCh38#34635156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82333646-C-A

34635157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82333647-T-C

34635195-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82333675-T-G

34635452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82333895-G-T

34635616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82333968-T-C

34635785-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82334011-G-C

34635785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron variant
orthologous variants: 82334011-G-T

http://identifiers.org/hco/17/GRCh38#34635799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82334031-C-A

34635799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82334031-C-T

34635803-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82334035-T-A

34635803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82334035-T-C

http://identifiers.org/hco/17/GRCh38#34635843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82334074-C-A

34635843-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82334074-C-G

34635843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82334074-C-T

34635868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82334097-T-C

http://identifiers.org/hco/17/GRCh38#34635876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82334105-C-A

34635876-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82334105-C-G

34635876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82334105-C-T

34635925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82334121-G-A

34635925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82334121-G-T

34635930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82334126-T-C

34635945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82334142-G-T

http://identifiers.org/hco/17/GRCh38#34635971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82334166-C-A

34635976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82334171-T-C

34635991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 82334182-T-C

34636018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 82334209-G-A

34636018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 82334209-G-T

http://identifiers.org/hco/17/GRCh38#34636085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82334276-C-A

34636085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82334276-C-T

34636126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 82334317-G-A

34636126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 82334317-G-T

34636222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82334421-G-A

34636281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82334476-G-A

34636296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82334491-G-A

34636296-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82334491-G-C

http://identifiers.org/hco/17/GRCh38#34636314-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82334509-A-C

http://identifiers.org/hco/17/GRCh38#34636348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82334519-C-A

http://identifiers.org/hco/17/GRCh38#34636349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82334520-C-A

34636349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82334520-C-T

34636558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82334692-G-T

34636615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82334701-G-A

http://identifiers.org/hco/17/GRCh38#34636971-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82334890-A-C

http://identifiers.org/hco/17/GRCh38#34637068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82334985-C-A

34637068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82334985-C-T

http://identifiers.org/hco/17/GRCh38#34637106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82335019-C-A

34637106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82335019-C-T

http://identifiers.org/hco/17/GRCh38#34637118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82335031-C-A

34637118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82335031-C-T

http://identifiers.org/hco/17/GRCh38#34637164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82335074-C-A

34637218-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 82335136-C-G

34637218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 82335136-C-T

34637236-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 82335154-C-G

34637314-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82335232-C-G

34637314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 82335232-C-T

34637411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82335329-C-T

34637452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 82335370-G-A

34637452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82335370-G-T

http://identifiers.org/hco/17/GRCh38#34637455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82335373-C-A

34637455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 82335373-C-T

34637479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 82335397-C-T

34637527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: synonymous variant
orthologous variants: 82335445-G-T

34637632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: synonymous variant
orthologous variants: 82335547-C-T

34637743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: synonymous variant
orthologous variants: 82335658-T-C

34637743-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: missense variant
orthologous variants: 82335658-T-G

34637756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: missense variant
orthologous variants: 82335671-C-T

34637776-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: synonymous variant
orthologous variants: 82335691-C-G

34637881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: synonymous variant
orthologous variants: 82335796-G-T

34637989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: synonymous variant
orthologous variants: 82335904-A-G

34638004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: synonymous variant
orthologous variants: 82335919-C-T

34638007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: synonymous variant
orthologous variants: 82335922-G-A

34638007-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: missense variant
orthologous variants: 82335922-G-T

34638217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: synonymous variant
orthologous variants: 82336129-C-T

http://identifiers.org/hco/17/GRCh38#34638351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82336264-C-A

34638351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 3 prime UTR variant
orthologous variants: 82336264-C-T

34638356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 3 prime UTR variant
orthologous variants: 82336273-G-A

34638442-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 82336331-T-G

34638477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 3 prime UTR variant
orthologous variants: 82336365-A-G

http://identifiers.org/hco/17/GRCh38#34638512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82336398-C-A

34638512-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 3 prime UTR variant
orthologous variants: 82336398-C-G

34638522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 3 prime UTR variant
orthologous variants: 82336408-C-T

34638616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 3 prime UTR variant
orthologous variants: 82336506-G-A

34638616-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 3 prime UTR variant
orthologous variants: 82336506-G-C

34638616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 3 prime UTR variant
orthologous variants: 82336506-G-T

34638649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 3 prime UTR variant
orthologous variants: 82336538-G-A

34638649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 3 prime UTR variant
orthologous variants: 82336538-G-T

http://identifiers.org/hco/17/GRCh38#34638769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82336657-C-A

34638769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 3 prime UTR variant
orthologous variants: 82336657-C-T

http://identifiers.org/hco/17/GRCh38#34638797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82336684-C-A

http://identifiers.org/hco/17/GRCh38#34638814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82336701-C-A

34638814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 3 prime UTR variant
orthologous variants: 82336701-C-T

34638856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 3 prime UTR variant
orthologous variants: 82336731-C-T

34638896-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 3 prime UTR variant
orthologous variants: 82336760-C-G

34638984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 3 prime UTR variant
orthologous variants: 82336849-G-A

34638984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 3 prime UTR variant
orthologous variants: 82336849-G-T

34639059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 3 prime UTR variant
orthologous variants: 82336907-C-T

34639070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 3 prime UTR variant
orthologous variants: 82336918-C-T

34639082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 3 prime UTR variant
orthologous variants: 82336930-G-T

34639150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 3 prime UTR variant
orthologous variants: 82336985-G-A

34639150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 3 prime UTR variant
orthologous variants: 82336985-G-T

34639155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 3 prime UTR variant
orthologous variants: 82336990-G-A

34639155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 3 prime UTR variant
orthologous variants: 82336990-G-T

http://identifiers.org/hco/17/GRCh38#34639187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82337022-C-A

34639196-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 3 prime UTR variant
orthologous variants: 82337034-C-G

http://identifiers.org/hco/17/GRCh38#34639277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#82337113-C-A

34639277-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 3 prime UTR variant
orthologous variants: 82337113-C-G

34639296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 3 prime UTR variant
orthologous variants: 82337131-G-A

34639296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26991
most severe consequence: 3 prime UTR variant
orthologous variants: 82337131-G-T