11676950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: 5 prime UTR variant
orthologous variants: 63509148-A-G

11677086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63509005-T-C

11677107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63508998-A-G

11677107-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63508998-A-T

11677112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63508993-G-A

11677112-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63508993-G-C

11677112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63508993-G-T

11677115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63508990-A-G

http://identifiers.org/hco/8/GRCh38#11677126-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63508975-A-C

11677242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63508871-G-A

11677340-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63508772-C-G

http://identifiers.org/hco/8/GRCh38#11677347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63508765-C-A

11677347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63508765-C-T

11677462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63508614-C-T

11677624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63508465-G-A

11677707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63508390-G-T

11677872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63508237-C-T

11677968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63508153-A-G

11678008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63508116-G-A

http://identifiers.org/hco/8/GRCh38#11678011-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63508113-A-C

11678135-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63508006-T-A

11678278-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63507895-G-C

11678503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63507705-T-C

11678609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63507606-C-T

11678810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63507441-C-T

11679239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63507039-T-C

11679431-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63506859-A-T

11679502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63506788-C-T

11679691-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63506655-G-C

11679691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63506655-G-T

11679904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63506448-T-C

11679946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63506406-T-C

11680050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63506323-G-T

11680055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63506318-G-A

11680179-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63506219-G-C

http://identifiers.org/hco/8/GRCh38#11680386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63506050-C-A

11680408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, undefined
orthologous variants: 63506019-G-A

http://identifiers.org/hco/8/GRCh38#11680426-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63505960-C-A

11680426-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63505960-C-G

11680426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63505960-C-T

11680473-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63505913-C-G

11680533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63505846-G-A

11680536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63505843-C-T

11680799-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, undefined
orthologous variants: 63505575-T-A

11680799-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, undefined
orthologous variants: 63505575-T-G

11680946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63505357-G-A

http://identifiers.org/hco/8/GRCh38#11681080-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63505217-A-C

11681080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63505217-A-G

11681083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63505214-G-A

11681083-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63505214-G-C

11681083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63505214-G-T

11681102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63505176-G-A

11681191-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63505100-C-G

11681203-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63505088-G-C

11681203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63505088-G-T

11681263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63505026-G-A

11681263-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63505026-G-C

11681263-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63505026-G-T

11681458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63504809-C-T

11681480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63504777-G-A

11681482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63504775-G-T

11681502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63504760-G-A

11681502-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63504760-G-C

11681502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63504760-G-T

11681508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63504754-G-A

11681508-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63504754-G-C

http://identifiers.org/hco/8/GRCh38#11681572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63504673-C-A

http://identifiers.org/hco/8/GRCh38#11681575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63504670-C-A

http://identifiers.org/hco/8/GRCh38#11681933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63504306-C-A

11681933-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63504306-C-G

11682220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63504044-A-G

11682275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63503989-C-T

http://identifiers.org/hco/8/GRCh38#11682309-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63503956-A-C

11682611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63503633-A-G

11682613-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63503631-A-T

11682758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63503324-A-G

11682758-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63503324-A-T

11682825-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63503270-G-C

11682961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63503141-G-A

11682961-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63503141-G-C

http://identifiers.org/hco/8/GRCh38#11683022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63503083-C-A

11683022-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63503083-C-G

11683051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63503053-C-T

11683055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63503049-G-T

11683118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63502942-G-A

11683120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63502940-G-A

11683120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63502940-G-T

http://identifiers.org/hco/8/GRCh38#11683265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63502781-C-A

11683265-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63502781-C-G

11683265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63502781-C-T

11683343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63502726-C-T

http://identifiers.org/hco/8/GRCh38#11683363-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63502707-C-A

11683363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63502707-C-T

11683532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63502581-G-A

11683532-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63502581-G-C

11683579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63502525-G-A

11684007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63502104-C-T

11684053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63502068-A-G

11684104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63502048-C-T

11685030-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63501205-C-G

11685054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63501178-T-C

11685119-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63501113-A-T

http://identifiers.org/hco/8/GRCh38#11685213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63500985-C-A

11685520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63500647-T-C

11685625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63500564-T-C

11685640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63500549-C-T

11686176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63500046-A-G

11686226-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63499985-T-G

11686256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63499963-A-G

11686256-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63499963-A-T

http://identifiers.org/hco/8/GRCh38#11686257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63499962-C-A

11686258-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63499961-A-T

11686310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63499913-C-T

11686509-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63499762-C-G

http://identifiers.org/hco/8/GRCh38#11686574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63499699-C-A

11686574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63499699-C-T

http://identifiers.org/hco/8/GRCh38#11686584-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63499689-A-C

11686625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63499655-G-A

11686643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63499637-T-C

11687499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63499138-G-T

http://identifiers.org/hco/8/GRCh38#11687864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63498787-C-A

11688110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63498536-C-T

11688188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63498461-G-A

11688188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63498461-G-T

11688634-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63497903-G-C

11688636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63497901-G-A

11688830-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63497736-C-G

11688830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63497736-C-T

11688839-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63497727-A-T

11688963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63497595-C-T

11689152-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63497407-G-C

11689392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63497246-G-T

11689429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63497207-G-A

11689622-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63497013-G-C

11689693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63496961-C-T

11689960-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63496752-T-A

11690169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63496566-A-G

11690169-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63496566-A-T

http://identifiers.org/hco/8/GRCh38#11690415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63495844-C-A

11690415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63495844-C-T

http://identifiers.org/hco/8/GRCh38#11691002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63495554-C-A

11691137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63495445-C-T

11691175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63495409-A-G

11691254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63494982-G-A

11692120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63493929-C-T

11692188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63493857-A-G

11692214-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63493830-G-C

11692528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63493616-C-T

11692785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63493478-G-A

11692985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63493264-C-T

http://identifiers.org/hco/8/GRCh38#11693166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63492999-C-A

11694394-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63491953-C-G

11694451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63491893-A-G

11694474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63491872-A-G

http://identifiers.org/hco/8/GRCh38#11694552-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63491754-A-C

11694552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63491754-A-G

http://identifiers.org/hco/8/GRCh38#11694612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63491689-C-A

11695795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63491252-A-G

11696221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63490908-G-A

11696247-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63490879-C-G

http://identifiers.org/hco/8/GRCh38#11696363-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63490756-A-C

11696499-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63490617-C-G

http://identifiers.org/hco/8/GRCh38#11696630-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63490478-C-A

11696630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63490478-C-T

11697105-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63489735-C-G

11697105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63489735-C-T

11697417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63489494-T-C

11697524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, undefined
orthologous variants: 63489422-A-G

http://identifiers.org/hco/8/GRCh38#11697588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63489358-C-A

11697735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63489220-C-T

http://identifiers.org/hco/8/GRCh38#11697739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63489216-C-A

11697739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63489216-C-T

11697913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63489031-C-T

11698165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63488781-C-T

11698244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63488713-T-C

11698263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63488705-A-G

11698730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63488207-T-C

11698995-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63487863-T-A

11699013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63487843-C-T

11699014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63487842-G-A

http://identifiers.org/hco/8/GRCh38#11699017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63487839-C-A

11699040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63487819-A-G

http://identifiers.org/hco/8/GRCh38#11699061-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63487767-C-A

11699061-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63487767-C-G

11699072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63487756-C-T

11699355-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63487525-C-G

11699386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63487489-C-T

11699480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63487408-G-A

11699524-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63487364-T-A

11699546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63487339-G-A

11699550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63487335-G-A

11699661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63487220-C-T

11699709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63487207-G-T

11699710-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63487206-C-G

11699909-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63487016-A-T

http://identifiers.org/hco/8/GRCh38#11699950-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63486985-A-C

11700015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63486930-G-A

11700015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63486930-G-T

11700071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63486885-G-A

11700403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63486458-C-T

11700409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63486442-A-G

http://identifiers.org/hco/8/GRCh38#11700439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63486423-C-A

11700439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63486423-C-T

11700463-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63486397-T-A

11700481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63486367-T-C

11700572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: 5 prime UTR variant
orthologous variants: 63486289-A-G

http://identifiers.org/hco/8/GRCh38#11700579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63486285-C-A

11700661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: 5 prime UTR variant
orthologous variants: 63486227-G-A

11700661-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: 5 prime UTR variant
orthologous variants: 63486227-G-T

11700700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: 5 prime UTR variant
orthologous variants: 63486182-T-C

11700706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: 5 prime UTR variant
orthologous variants: 63486176-T-C

11700706-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: 5 prime UTR variant
orthologous variants: 63486176-T-G

11700739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: 5 prime UTR variant
orthologous variants: 63486147-G-A

11700739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: 5 prime UTR variant
orthologous variants: 63486147-G-T

11700741-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: 5 prime UTR variant
orthologous variants: 63486145-G-T

11700758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: 5 prime UTR variant
orthologous variants: 63486130-G-T

11700777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: 5_prime_UTR_variant, splice_region_variant
orthologous variants: 63486111-A-G

11700814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63486075-T-C

11700831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63486058-T-C

11700875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63486007-A-G

11700903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63485970-G-A

11700903-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63485970-G-C

11701110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63485699-G-A

11701197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63485615-T-C

11701237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63485572-G-T

11701274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63485534-G-A

11701296-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63485516-C-G

11701334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63485477-A-G

11701620-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63485214-A-T

11701956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63484910-G-A

11702013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63484882-C-T

11702060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63484851-G-A

11702060-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63484851-G-C

11702578-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63484324-T-A

11702617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63484280-G-A

11702749-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63484146-G-C

11702762-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63484133-C-G

http://identifiers.org/hco/8/GRCh38#11702779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63484116-C-A

11703057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63483833-G-T

11703253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63483637-T-C

http://identifiers.org/hco/8/GRCh38#11703634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63483251-C-A

11703665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63483220-C-T

http://identifiers.org/hco/8/GRCh38#11703676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63483209-C-A

11703775-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, undefined
orthologous variants: 63483121-G-C

11703819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63483077-A-G

11704025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63482886-A-G

http://identifiers.org/hco/8/GRCh38#11704109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#63482801-C-A

11704109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, undefined
orthologous variants: 63482801-C-T

http://identifiers.org/hco/8/GRCh38#11704167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63482747-C-A

11704247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 63482661-G-A

11704247-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 63482661-G-C

11704258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 63482650-T-C

11704363-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63482545-T-A

11704597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63482310-C-T

11704792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63482142-C-T

11704793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63482141-C-T

11704801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63482133-C-T

11704895-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63482042-A-T

11704960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63481985-C-T

11704983-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63481962-A-T

11705018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63481925-G-A

11705066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63481869-G-A

11705147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63481787-C-T

11705261-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63481681-C-G

11705401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63481582-C-T

11705794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63481209-A-G

11705816-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63481187-A-T

11705823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63481178-T-C

11705941-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 63481059-T-A

11705941-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 63481059-T-G

11705954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 63481042-G-T

11705985-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 63481012-T-A

11706411-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63480504-T-G

11706597-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63480355-C-G

11706597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63480355-C-T

11706848-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63480138-C-G

11706866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63480120-T-C

11706984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63479998-A-G

11707122-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63479902-T-A

11707122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63479902-T-C

11707122-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63479902-T-G

11707124-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63479900-G-T

http://identifiers.org/hco/8/GRCh38#11707182-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63479842-A-C

11707316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63479696-G-T

11707350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63479625-G-T

11707701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63479242-C-T

http://identifiers.org/hco/8/GRCh38#11707707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63479236-C-A

11707707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63479236-C-T

11707765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63479182-A-G

http://identifiers.org/hco/8/GRCh38#11707768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63479179-C-A

11707768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63479179-C-T

11707816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63479132-G-A

http://identifiers.org/hco/8/GRCh38#11707818-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63479130-A-C

11707818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63479130-A-G

11707833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63479115-T-C

11707861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 63479087-C-T

http://identifiers.org/hco/8/GRCh38#11707921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63478986-C-A

11707995-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 63478920-C-G

http://identifiers.org/hco/8/GRCh38#11708055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63478873-C-A

11708055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 63478873-C-T

11708121-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 63478802-A-T

11708124-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 63478799-C-G

11708124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 63478799-C-T

11708140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 63478782-G-A

11708140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 63478782-G-T

11708200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 63478656-G-A

http://identifiers.org/hco/8/GRCh38#11708260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63478615-C-A

http://identifiers.org/hco/8/GRCh38#11708371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63478537-C-A

11708371-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, missense_variant
orthologous variants: 63478537-C-G

11708371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, missense_variant
orthologous variants: 63478537-C-T

11708404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, missense_variant
orthologous variants: 63478504-G-A

11708404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, missense_variant
orthologous variants: 63478504-G-T

http://identifiers.org/hco/8/GRCh38#11708405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63478503-C-A

11708405-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 63478503-C-G

11708405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 63478503-C-T

http://identifiers.org/hco/8/GRCh38#11708497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63478411-C-A

11708497-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, missense_variant
orthologous variants: 63478411-C-G

11708497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, missense_variant
orthologous variants: 63478411-C-T

11708503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, missense_variant
orthologous variants: 63478405-G-A

11708503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, missense_variant
orthologous variants: 63478405-G-T

11708526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, missense_variant
orthologous variants: 63478382-G-A

11708526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, missense_variant
orthologous variants: 63478382-G-T

11708542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, missense_variant
orthologous variants: 63478366-G-A

11708542-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, missense_variant
orthologous variants: 63478366-G-C

11708542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, missense_variant
orthologous variants: 63478366-G-T

11708544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, missense_variant
orthologous variants: 63478364-G-A

11708544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, missense_variant
orthologous variants: 63478364-G-T

11708694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, missense_variant
orthologous variants: 63478214-G-A

11708694-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, missense_variant
orthologous variants: 63478214-G-C

11708694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, undefined
orthologous variants: 63478214-G-T

11708707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, missense_variant
orthologous variants: 63478201-A-G

11708721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, missense_variant
orthologous variants: 63478187-G-A

11708721-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, missense_variant
orthologous variants: 63478187-G-C

11708721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, undefined
orthologous variants: 63478187-G-T

11708775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, missense_variant
orthologous variants: 63478133-G-A

11708775-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, missense_variant
orthologous variants: 63478133-G-C

11708775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, missense_variant
orthologous variants: 63478133-G-T

11708802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, missense_variant
orthologous variants: 63478106-G-A

11708802-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, missense_variant
orthologous variants: 63478106-G-C

11708802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, missense_variant
orthologous variants: 63478106-G-T

11708835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, missense_variant
orthologous variants: 63478073-G-A

11708835-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, missense_variant
orthologous variants: 63478073-G-C

11708835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, missense_variant
orthologous variants: 63478073-G-T

11708862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, missense_variant
orthologous variants: 63478046-T-C

http://identifiers.org/hco/8/GRCh38#11708956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63477974-C-A

11708956-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63477974-C-G

11708956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63477974-C-T

http://identifiers.org/hco/8/GRCh38#11708986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63477959-C-A

11708986-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63477959-C-G

11708986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63477959-C-T

11708995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63477950-G-T

11709044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63477906-T-C

11709044-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63477906-T-G

http://identifiers.org/hco/8/GRCh38#11709513-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63477543-A-C

11709513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63477543-A-G

11709594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63477470-G-A

11709594-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63477470-G-C

11709594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63477470-G-T

11709600-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63477464-T-A

11709600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63477464-T-C

11709600-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63477464-T-G

11709631-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63477439-C-G

http://identifiers.org/hco/8/GRCh38#11711867-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63475996-A-C

11712044-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63475818-T-A

11712070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63475792-T-C

11712204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63475701-C-T

11713108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63475178-T-C

11713117-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63475169-T-A

11713166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63475118-G-A

11713166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63475118-G-T

11713389-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63474898-A-T

11713627-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63474659-T-A

11713628-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63474658-T-A

11713681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63474588-G-T

11713700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63474563-T-C

11713772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63474488-T-C

http://identifiers.org/hco/8/GRCh38#11713811-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63474439-A-C

11713811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63474439-A-G

11714114-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63473879-G-C

11714190-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63473804-T-G

11714427-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63473577-C-G

http://identifiers.org/hco/8/GRCh38#11714531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63473455-C-A

11714665-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63473321-C-G

11714665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63473321-C-T

11715275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63472740-A-G

11715784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63472371-T-C

11715792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63472369-A-G

11715793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63472368-G-A

11715813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63472350-A-G

11715891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63472294-G-A

11716088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63472106-A-G

11716449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63471633-G-A

http://identifiers.org/hco/8/GRCh38#11716740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63471392-C-A

11716740-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63471392-C-G

11717379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63470231-T-C

11717407-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63470212-A-T

11717788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63469895-C-T

11717843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63469835-C-T

11717950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63469742-G-A

11718067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63469633-T-C

11718176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63469538-C-T

11718380-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63469345-C-G

11718380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63469345-C-T

11718513-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63469205-G-C

11719235-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63468565-A-T

11719269-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63468531-C-G

11719379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63468425-C-T

11719423-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63468365-A-T

11719637-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63468169-C-G

11719854-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63467951-T-G

11724570-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63461793-C-G

11726967-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, undefined
orthologous variants: 63460465-C-G

11726987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, undefined
orthologous variants: 63460446-C-T

11727204-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63460235-A-T

11727299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63460140-C-T

11727319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63460126-G-A

11727570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63459881-C-T

11732550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63456561-T-C

http://identifiers.org/hco/8/GRCh38#11732586-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63456525-A-C

11732836-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63456296-C-G

11732847-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63456288-C-G

11733284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63455963-A-G

11733284-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63455963-A-T

11733514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63455730-G-T

http://identifiers.org/hco/8/GRCh38#11733541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63455705-C-A

11733542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63455704-A-G

11733542-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63455704-A-T

11734768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63454255-G-A

11734839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63454182-G-A

11735041-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63454022-G-C

11735156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63453855-T-C

11735291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63453688-G-A

11735325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63453656-T-C

11737005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63453017-T-C

11737108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63452916-A-G

11737244-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63452781-C-G

11737534-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63452488-A-T

11737588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63452377-G-T

11737592-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63452373-G-C

11737593-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63452366-G-C

11737634-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63452307-T-G

11737704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63452258-A-G

11737764-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63452214-G-C

http://identifiers.org/hco/8/GRCh38#11737765-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63452213-A-C

http://identifiers.org/hco/8/GRCh38#11737851-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63452142-A-C

11737852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63452141-G-T

11737867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63452125-A-G

11737867-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63452125-A-T

http://identifiers.org/hco/8/GRCh38#11738208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63451691-C-A

11738208-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63451691-C-G

http://identifiers.org/hco/8/GRCh38#11738221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63451678-C-A

11738221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63451678-C-T

11738231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63451666-A-G

11738247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63451651-T-C

11738332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63451570-C-T

11738418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63451439-C-T

11738422-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63451435-G-C

http://identifiers.org/hco/8/GRCh38#11738431-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63451425-A-C

11738538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63451310-A-G

11738558-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63451290-T-A

11738726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63451126-A-G

11738784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63451059-C-T

11738806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63451041-C-T

11738974-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63450862-C-G

11739003-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63450840-C-G

11739074-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63450773-T-A

11739551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63450002-G-A

11739835-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, undefined
orthologous variants: 63449735-C-G

11739946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63449635-C-T

11739967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63449606-G-A

11739984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63449589-G-A

11741760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63449138-G-A

11741761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63449137-A-G

11742494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63448192-G-A

11742521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63448160-G-A

11742551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63448120-G-A

11742619-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63448055-G-C

11742698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63447978-G-A

11742800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63447872-C-T

11743087-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63447604-A-T

11743089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63447602-G-A

11743089-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63447602-G-C

11743135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63447554-G-A

11743339-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63447337-G-C

11743340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63447336-G-A

11743376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63447308-C-T

11743464-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63447219-T-A

11743561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63447094-A-G

11743625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63447035-C-T

11743664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63446988-T-C

11743793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63446896-C-T

11743886-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63446828-A-T

11744005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63446744-C-T

11744006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63446743-C-T

11744382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63446389-G-A

11744382-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63446389-G-C

11744432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63446299-G-T

11744457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63446256-C-T

11744489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63446238-T-C

11744820-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63445432-G-C

11744950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63445290-C-T

11745170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63445068-G-T

11745224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63445014-G-A

11745255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63444979-C-T

11745279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63444952-G-A

11745286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63444945-G-A

11746655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63444635-G-A

11746779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63444537-G-A

11746874-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63444449-T-A

11747056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63444290-C-T

11747115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63444239-G-A

11747448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63443910-C-T

11747503-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63443855-T-G

11748489-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63442913-C-G

11748555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63442483-T-C

11748636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63442416-A-G

11748771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63442306-G-A

11748771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63442306-G-T

11748829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63442274-T-C

11749047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: missense variant
orthologous variants: 63442074-G-A

11749047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: missense variant
orthologous variants: 63442074-G-T

11749115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63442008-G-A

11749133-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63441982-C-G

11749178-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63441946-G-C

11749401-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63441753-A-T

11749424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63441741-T-C

11749502-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63441689-A-T

11749561-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63441627-T-A

11749561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63441627-T-C

11749562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63441626-T-C

11749591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63441597-G-A

11749687-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63441456-T-A

11749760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63441418-G-A

http://identifiers.org/hco/8/GRCh38#11750231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63441111-C-A

11750270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63441073-C-T

11750276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63441067-G-A

11750289-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63441053-C-G

11750289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63441053-C-T

http://identifiers.org/hco/8/GRCh38#11754997-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63440887-A-C

11754997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63440887-A-G

11754997-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63440887-A-T

11755124-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: missense_variant, undefined
orthologous variants: 63440767-A-T

http://identifiers.org/hco/8/GRCh38#11755197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#63440695-C-A

11755197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, undefined
orthologous variants: 63440695-C-T

11755239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, undefined
orthologous variants: 63440654-G-A

11755239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, undefined
orthologous variants: 63440654-G-T

http://identifiers.org/hco/8/GRCh38#11755249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63440644-C-A

11755249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63440644-C-T

http://identifiers.org/hco/8/GRCh38#11755261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63440638-C-A

11755261-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63440638-C-G

11755399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63440555-A-G

http://identifiers.org/hco/8/GRCh38#11755420-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63440534-A-C

11755433-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63440521-C-G

11755453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63440502-C-T

11755457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63440498-G-T

11755569-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63440434-A-T

11755592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63440412-T-C

11755594-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63440410-C-G

http://identifiers.org/hco/8/GRCh38#11755650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63440366-C-A

11755773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63440264-A-G

11755790-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63440247-C-G

http://identifiers.org/hco/8/GRCh38#11756080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63440089-C-A

11756080-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63440089-C-G

http://identifiers.org/hco/8/GRCh38#11756164-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63440014-A-C

11756205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63439975-G-A

11756227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63439954-A-G

11756249-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63439932-T-G

11756320-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63439872-C-G

http://identifiers.org/hco/8/GRCh38#11756367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63439818-C-A

11756367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63439818-C-T

http://identifiers.org/hco/8/GRCh38#11756403-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63439786-C-A

11756428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63439761-A-G

11756428-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63439761-A-T

http://identifiers.org/hco/8/GRCh38#11756431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63439758-C-A

http://identifiers.org/hco/8/GRCh38#11756432-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63439757-A-C

11756432-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63439757-A-T

11756436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63439753-G-A

11756436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63439753-G-T

11756442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63439747-G-A

11756442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron variant
orthologous variants: 63439747-G-T

11756503-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63439686-T-G

11756533-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63439658-T-A

http://identifiers.org/hco/8/GRCh38#11756584-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63439608-A-C

11756584-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63439608-A-T

11756604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63439588-A-G

11756653-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63439542-G-C

http://identifiers.org/hco/8/GRCh38#11756682-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63439501-A-C

11756749-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 63439307-T-A

11756749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 63439307-T-C

11756749-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 63439307-T-G

11756779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 63439276-G-A

11756779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 63439276-G-T

11756885-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 63439133-T-A

11756897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63439121-G-T

11756967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63439050-A-G

11756968-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63439049-G-C

11757087-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63438921-C-G

11757087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63438921-C-T

11757163-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63438877-T-A

11757173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63438866-A-G

11757235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63438822-G-A

11757235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63438822-G-T

11757730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63438447-G-A

11757730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63438447-G-T

11758018-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63438213-C-G

11758018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63438213-C-T

11758109-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63438127-C-G

http://identifiers.org/hco/8/GRCh38#11758244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63438042-C-A

11758244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63438042-C-T

11758308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63437989-G-A

11758359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63437938-C-T

11758435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63437862-T-C

http://identifiers.org/hco/8/GRCh38#11758772-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63437480-A-C

11758772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: 3 prime UTR variant
orthologous variants: 63437480-A-G

http://identifiers.org/hco/8/GRCh38#11758873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63437396-C-A

11758873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: 3 prime UTR variant
orthologous variants: 63437396-C-T

http://identifiers.org/hco/8/GRCh38#11758887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63437382-C-A

11758887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: 3 prime UTR variant
orthologous variants: 63437382-C-T

http://identifiers.org/hco/8/GRCh38#11758909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63437371-C-A

11758909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: 3 prime UTR variant
orthologous variants: 63437371-C-T

http://identifiers.org/hco/8/GRCh38#11759070-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63437198-A-C

11759070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: 3 prime UTR variant
orthologous variants: 63437198-A-G

11759070-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: 3 prime UTR variant
orthologous variants: 63437198-A-T

http://identifiers.org/hco/8/GRCh38#11759262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#63437074-C-A

11759262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 63437074-C-T

http://identifiers.org/hco/8/GRCh38#11759268-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#63437068-C-A

11759268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 63437068-C-T

http://identifiers.org/hco/8/GRCh38#11759355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63436986-C-A

11759355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: 3 prime UTR variant
orthologous variants: 63436986-C-T

11759449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: 3 prime UTR variant
orthologous variants: 63436894-T-C

11759657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: 3 prime UTR variant
orthologous variants: 63436699-G-A

11759657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: 3 prime UTR variant
orthologous variants: 63436699-G-T

11759790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: 3 prime UTR variant
orthologous variants: 63436575-C-T

11759846-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4173
most severe consequence: 3 prime UTR variant
orthologous variants: 63436522-T-A