82483214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 100225769-A-G

82483236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 100225791-T-C

82483277-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 100225835-G-C

82483355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: 3 prime UTR variant
orthologous variants: 100225904-G-A

82483355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: 3 prime UTR variant
orthologous variants: 100225904-G-T

http://identifiers.org/hco/4/GRCh38#82483394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100225954-C-A

82483447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: 3 prime UTR variant
orthologous variants: 100226006-C-T

http://identifiers.org/hco/4/GRCh38#82483473-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100226033-C-A

82483627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: 3 prime UTR variant
orthologous variants: 100226170-C-T

82483923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: 3 prime UTR variant
orthologous variants: 100226354-G-A

82483923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: 3 prime UTR variant
orthologous variants: 100226354-G-T

82483924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: 3 prime UTR variant
orthologous variants: 100226355-G-A

82483924-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: 3 prime UTR variant
orthologous variants: 100226355-G-T

82483992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: 3 prime UTR variant
orthologous variants: 100226393-A-G

http://identifiers.org/hco/4/GRCh38#82484197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100226481-C-A

82484197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: 3 prime UTR variant
orthologous variants: 100226481-C-T

http://identifiers.org/hco/4/GRCh38#82484278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100226543-C-A

82484279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: 3 prime UTR variant
orthologous variants: 100226544-T-C

82484402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: 3 prime UTR variant
orthologous variants: 100226644-C-T

82484450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: 3 prime UTR variant
orthologous variants: 100226681-A-G

82484469-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: 3 prime UTR variant
orthologous variants: 100226697-C-G

82484488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: 3 prime UTR variant
orthologous variants: 100226716-A-G

82484579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: 3 prime UTR variant
orthologous variants: 100226809-G-T

82484608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: 3 prime UTR variant
orthologous variants: 100226837-G-A

http://identifiers.org/hco/4/GRCh38#82484680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100226895-C-A

http://identifiers.org/hco/4/GRCh38#82484794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100227009-C-A

82484803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: 3 prime UTR variant
orthologous variants: 100227017-G-A

82484829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: 3 prime UTR variant
orthologous variants: 100227041-T-C

82484903-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: 3 prime UTR variant
orthologous variants: 100227119-T-A

82484903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: 3 prime UTR variant
orthologous variants: 100227119-T-C

http://identifiers.org/hco/4/GRCh38#82484944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100227160-C-A

82484944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: 3 prime UTR variant
orthologous variants: 100227160-C-T

http://identifiers.org/hco/4/GRCh38#82484970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100227186-C-A

82484997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: 3 prime UTR variant
orthologous variants: 100227209-G-A

82484997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: 3 prime UTR variant
orthologous variants: 100227209-G-T

82485104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: 3 prime UTR variant
orthologous variants: 100227284-A-G

82485119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: 3 prime UTR variant
orthologous variants: 100227299-G-T

82485206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: 3 prime UTR variant
orthologous variants: 100227395-T-C

82485206-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: 3 prime UTR variant
orthologous variants: 100227395-T-G

82485313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: 3 prime UTR variant
orthologous variants: 100227503-G-A

82485313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: 3 prime UTR variant
orthologous variants: 100227503-G-T

82485353-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: 3 prime UTR variant
orthologous variants: 100227543-A-T

82485398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: 3 prime UTR variant
orthologous variants: 100227588-G-A

82485410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: 3 prime UTR variant
orthologous variants: 100227606-G-A

82485411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: 3 prime UTR variant
orthologous variants: 100227607-T-C

82485443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: 3 prime UTR variant
orthologous variants: 100227646-G-A

82485443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: 3 prime UTR variant
orthologous variants: 100227646-G-T

82485486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: 3 prime UTR variant
orthologous variants: 100227689-T-C

82485586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: synonymous variant
orthologous variants: 100227787-A-G

82485851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100228004-T-C

82485851-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100228004-T-G

82485933-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100228081-C-G

82486828-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100228689-G-C

82486835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100228696-T-C

82486836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100228697-A-G

82487019-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100228901-C-G

82487084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: -G-A

82487454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: -A-G

http://identifiers.org/hco/4/GRCh38#82489277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100230278-C-A

82489433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100230406-G-T

http://identifiers.org/hco/4/GRCh38#82489568-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100230533-A-C

82489680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100230637-T-C

82489680-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100230637-T-G

82489788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100230737-C-T

82489914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100230864-G-A

82489914-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100230864-G-C

82489914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100230864-G-T

82489940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100230897-C-T

http://identifiers.org/hco/4/GRCh38#82490051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100231423-C-A

82490071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 100231443-A-G

82490086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: 3_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 100231458-T-C

82490103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 100231475-G-A

82490179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: 3_prime_UTR_variant, splice_donor_variant, synonymous_variant
orthologous variants: 100231551-T-C

82490292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100231635-G-A

82490292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100231635-G-T

82490318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100231654-G-A

82490318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100231654-G-T

82490363-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100231696-T-G

82490371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100231704-G-T

http://identifiers.org/hco/4/GRCh38#82492642-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100232329-A-C

82492943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100232428-G-A

82493185-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100232528-C-G

82493215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100232560-T-C

82493387-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100232745-T-A

82493453-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100232809-T-G

82493455-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100232811-C-G

82493647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100232979-A-G

82493718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100233035-C-T

82493893-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100233162-T-G

82494230-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100233423-G-C

82496116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: synonymous_variant, undefined
orthologous variants: 100234034-C-T

82496254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron_variant, undefined
orthologous variants: 100234169-G-T

82496524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100235615-C-T

82497775-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100236915-C-G

82497826-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100236969-G-C

82497829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100236972-T-C

82497941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100237057-G-A

82498659-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100237208-G-C

82498819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100237373-C-T

82498885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100237431-A-G

82499006-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100237521-A-T

82499745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100238453-G-A

82499745-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100238453-G-C

82499745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100238453-G-T

82499839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100238545-C-T

82499942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100238646-A-G

82500427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron_variant, undefined
orthologous variants: 100239134-A-G

82500585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100239292-A-G

82500693-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100239392-C-G

82500713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100239411-G-T

82500763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100239461-G-A

82500814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100239513-A-G

82500940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100239637-G-A

82500979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100239677-G-A

82501018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100239722-G-A

82502143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100240105-A-G

http://identifiers.org/hco/4/GRCh38#82502638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100240540-C-A

82502638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100240540-C-T

82502779-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: missense variant
orthologous variants: 100240678-A-T

82502840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100240737-A-G

82502871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100240773-G-A

82503124-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100240983-G-C

82503124-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100240983-G-T

82503130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100240999-G-A

82503130-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100240999-G-C

82503130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100240999-G-T

http://identifiers.org/hco/4/GRCh38#82503202-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100241081-A-C

82504061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100242951-G-A

http://identifiers.org/hco/4/GRCh38#82504085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100242977-C-A

82504144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100243025-G-T

82504637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: synonymous variant
orthologous variants: 100243525-G-A

82504687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100243575-T-C

82505390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100243776-T-C

82505517-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100243888-C-G

82505517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100243888-C-T

82505584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100243943-A-G

82508878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100256790-A-G

82509526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100257319-T-C

82509532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100257325-A-G

http://identifiers.org/hco/4/GRCh38#82510821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100258273-C-A

82510909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100258340-G-A

82511152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100258576-T-C

http://identifiers.org/hco/4/GRCh38#82511248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100258669-C-A

82511348-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100258789-G-C

82511378-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100258819-T-G

http://identifiers.org/hco/4/GRCh38#82511568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100258920-C-A

82511965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100259053-T-C

82511965-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100259053-T-G

82512179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100259273-C-T

82512415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100259480-T-C

82512451-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100259513-C-G

82512544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100259603-C-T

82514938-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100261661-T-G

82515241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100261884-C-T

82515295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100261920-T-C

82515298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100261923-G-A

82515834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100262376-A-G

http://identifiers.org/hco/4/GRCh38#82515896-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100262411-C-A

82516202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100262700-G-A

82516260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100262747-G-A

82516313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100262798-G-T

82516365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100262848-A-G

82516381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100262864-G-A

82516532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100262966-C-T

82516856-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100263153-T-A

82516856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100263153-T-C

82516890-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100263181-A-T

82516919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100263210-A-G

http://identifiers.org/hco/4/GRCh38#82516980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100263265-C-A

82517176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100263469-T-C

82517711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100265030-G-A

82517812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100265114-A-G

82517917-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100265209-G-C

82517954-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100265246-A-T

82519004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100266404-T-C

82520016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100268545-G-A

82520033-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100268562-T-G

82524317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100272075-A-G

82524458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100272219-T-C

82524853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100272654-T-C

82524930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100272774-C-T

82525253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100273246-G-A

82525323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron_variant, undefined
orthologous variants: 100273310-A-G

82525337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron_variant, undefined
orthologous variants: 100273325-T-C

82525616-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100273619-C-G

82526570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100274523-A-G

82526645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100274586-A-G

http://identifiers.org/hco/4/GRCh38#82526686-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100274635-A-C

82526789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100274737-G-A

82526983-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100274912-G-C

82527067-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100275001-T-A

82527187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100275121-T-C

82527270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100275208-T-C

82527365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100275285-G-A

http://identifiers.org/hco/4/GRCh38#82527522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100275444-C-A

82527540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100275468-G-A

82527540-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100275468-G-C

82527565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100275492-T-C

82527591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100275520-G-A

82527603-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100275533-C-G

82527685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100275617-A-G

82527727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100275666-C-T

82527791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100275737-G-A

82527924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100275868-C-T

82528036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100275993-C-T

82528037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100275994-A-G

82528096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100276048-T-C

82528188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100276140-A-G

http://identifiers.org/hco/4/GRCh38#82528271-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100276368-A-C

82528271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100276368-A-G

82528295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100276391-G-A

82528595-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100276656-T-G

82532422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100285524-C-T

http://identifiers.org/hco/4/GRCh38#82532474-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100285575-A-C

82532537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100285733-T-C

82532567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100285762-G-A

82532567-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100285762-G-C

82532641-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100285832-T-G

82552531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100297753-C-T

82552533-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100297754-T-A

82553127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100298240-C-T

82553237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100298342-G-A

82553385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100298454-T-C

http://identifiers.org/hco/4/GRCh38#82553441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100298507-C-A

82553508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100298565-T-C

82553647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100299262-A-G

82554398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100300140-C-T

82555052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100301951-C-T

82555506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100302452-G-A

http://identifiers.org/hco/4/GRCh38#82555513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100302459-C-A

82555567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100302508-A-G

82555713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100302652-A-G

82555899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100302814-T-C

82555899-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100302814-T-G

82556340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100303039-G-A

82556889-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100303349-T-A

82556889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100303349-T-C

82557247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100303688-G-A

82557274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100303714-T-C

82557591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100304024-T-C

82558056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100304144-G-T

82558098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100304179-A-G

82558266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100304341-A-G

82559892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100305095-T-C

82559915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100305116-C-T

82560013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100305165-T-C

82560045-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100305188-C-G

82560073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100305214-G-A

http://identifiers.org/hco/4/GRCh38#82560117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100305256-C-A

82560117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100305256-C-T

82560320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100305439-T-C

82560549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100305936-G-A

82560549-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100305936-G-C

82560551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100305938-C-T

82560881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100306282-G-A

82560935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100306337-C-T

82561455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100306804-G-A

82561523-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100306853-C-G

82561523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100306853-C-T

82561614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100306916-G-T

82561693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100306946-C-T

82561834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100307021-G-A

82561834-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100307021-G-T

82561876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100307048-C-T

82562028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100307189-G-A

82562028-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100307189-G-C

82562028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100307189-G-T

82562043-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100307195-T-A

82562043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100307195-T-C

http://identifiers.org/hco/4/GRCh38#82562141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100307293-C-A

82562141-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100307293-C-G

82562141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: intron variant
orthologous variants: 100307293-C-T

http://identifiers.org/hco/4/GRCh38#82562164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: 5_prime_UTR_variant, missense_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100307332-C-A

82562164-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: 5_prime_UTR_variant, missense_variant, splice_region_variant
orthologous variants: 100307332-C-G

82562164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: 5_prime_UTR_variant, missense_variant, splice_region_variant
orthologous variants: 100307332-C-T

82562177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 100307345-G-T

http://identifiers.org/hco/4/GRCh38#82562355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100307522-C-A

82562355-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: 5 prime UTR variant
orthologous variants: 100307522-C-G

82562355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37263
most severe consequence: 5 prime UTR variant
orthologous variants: 100307522-C-T