http://identifiers.org/hco/16/GRCh38#77788584-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114932372-A-C

77788584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114932372-A-G

77788584-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114932372-A-T

77788751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 114932524-G-A

77788751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 114932524-G-T

http://identifiers.org/hco/16/GRCh38#77788756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114932529-C-A

77788756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 114932529-C-T

77788763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 114932536-C-T

77788817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 114932584-G-A

77788817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 114932584-G-T

77788838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 114932605-G-A

77788838-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 114932605-G-C

77788838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 114932605-G-T

http://identifiers.org/hco/16/GRCh38#77788954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114932720-C-A

77788954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114932720-C-T

77788995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114932763-G-A

77788995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114932763-G-T

http://identifiers.org/hco/16/GRCh38#77789016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114932794-C-A

77789016-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114932794-C-G

77789248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114933023-T-C

77789248-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114933023-T-G

77789313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114933151-G-A

77789410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114933242-G-A

http://identifiers.org/hco/16/GRCh38#77789562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114933379-C-A

77789712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114933524-G-A

77789795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114933602-T-C

77789881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114933703-G-A

http://identifiers.org/hco/16/GRCh38#77789889-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114933711-C-A

77790005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114933790-C-T

http://identifiers.org/hco/16/GRCh38#77790011-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114933797-A-C

77790011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114933797-A-G

77790074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114933864-A-G

77790100-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114933892-G-C

77790239-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114934028-G-C

77790261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114934053-T-C

77790392-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114934204-C-G

77790652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114934443-A-G

77790653-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114934444-T-A

77790672-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114934470-T-A

77790676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114934474-T-C

77790678-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114934476-C-G

77790678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114934476-C-T

77790706-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114934519-A-T

77790742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114934555-T-C

77790802-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114934635-T-A

77790808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114934641-T-C

77790951-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114934865-C-G

77790999-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114934916-A-T

77791009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114934926-A-G

77791067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114934985-T-C

http://identifiers.org/hco/16/GRCh38#77791116-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114935028-A-C

77791342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114935269-C-T

http://identifiers.org/hco/16/GRCh38#77791365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114935288-C-A

77792017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114935990-C-T

77792046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114936018-G-A

77792334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114936110-A-G

http://identifiers.org/hco/16/GRCh38#77792344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114936123-C-A

77792380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114936158-G-A

77792381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114936159-G-A

77792381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114936159-G-T

77792567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114936316-G-A

77792599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114936341-G-A

77793520-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114936785-G-C

77793571-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114936837-C-G

77793669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114936935-T-C

77793754-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114937020-T-A

77793784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114937050-G-A

77793924-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114937183-C-G

77794035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114937246-G-A

77794071-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114937288-C-G

77794071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114937288-C-T

77794341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114937540-C-T

http://identifiers.org/hco/16/GRCh38#77794396-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114937577-A-C

77794422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114937603-C-T

http://identifiers.org/hco/16/GRCh38#77794463-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114937626-A-C

http://identifiers.org/hco/16/GRCh38#77794507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114937679-C-A

77794620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114937792-A-G

77794787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114937984-G-T

77794814-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114938019-G-C

77795105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114938789-T-C

77795542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114939160-G-T

77796154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114939784-G-T

77796249-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114939884-G-C

77796392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114940025-C-T

77796530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114940165-T-C

77796552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114940187-A-G

http://identifiers.org/hco/16/GRCh38#77797483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114940794-C-A

77797762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114941025-G-A

77797762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114941025-G-T

77797805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114941067-A-G

77797883-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114941139-G-C

77797952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114941208-C-T

77798126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114941399-A-G

77798218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114941497-C-T

77798255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114941534-G-A

http://identifiers.org/hco/16/GRCh38#77798371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114941624-C-A

77798371-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114941624-C-G

77798432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114941686-T-C

77798618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114942366-C-T

http://identifiers.org/hco/16/GRCh38#77798649-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114942441-A-C

77798765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114942529-T-C

77798825-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114942589-G-C

77798864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114942624-G-A

77798864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114942624-G-T

77798892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114942652-C-T

77799801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114943764-T-C

77799917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114943848-G-T

77799925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114943856-A-G

77799995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114943932-G-A

77799995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114943932-G-T

77800039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114944000-G-A

77800039-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114944000-G-T

77800173-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114944122-C-G

77800225-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114944189-T-G

http://identifiers.org/hco/16/GRCh38#77800241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114944205-C-A

77800278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114944242-C-T

77800354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114944318-A-G

http://identifiers.org/hco/16/GRCh38#77800480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114944398-C-A

77800480-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114944398-C-G

77800495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114944412-G-A

77800495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114944412-G-T

77800606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114944520-C-T

77800619-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114944533-C-G

http://identifiers.org/hco/16/GRCh38#77800655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114944567-C-A

77800662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114944574-C-T

77800668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114944580-G-T

77801468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114945036-C-T

77801672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114945213-G-T

http://identifiers.org/hco/16/GRCh38#77801827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114945339-C-A

77801988-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114945504-G-C

http://identifiers.org/hco/16/GRCh38#77801997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114945513-C-A

77802074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114945574-T-C

77802118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114945640-G-A

77802118-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114945640-G-C

77802185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114945686-T-C

77802218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114945720-T-C

77802230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114945731-A-G

77802230-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114945731-A-T

77802235-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114945736-T-G

http://identifiers.org/hco/16/GRCh38#77802236-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114945737-A-C

77802266-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114945767-G-C

77803154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114946684-G-T

77803852-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114947458-T-A

77803912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114947516-C-T

77803913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114947517-G-A

http://identifiers.org/hco/16/GRCh38#77803969-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114947571-A-C

77803993-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114947595-G-C

77804031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114947633-G-A

77804070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114947674-C-T

http://identifiers.org/hco/16/GRCh38#77804215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114947818-C-A

77804215-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114947818-C-G

77804316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114947919-A-G

77804457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114948051-G-A

77804476-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114948070-T-G

77804513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114948107-G-T

77804581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114948174-C-T

http://identifiers.org/hco/16/GRCh38#77805183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114948495-C-A

77805607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114948898-C-T

77805743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114949004-C-T

77805845-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114949121-A-T

77805853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114949129-C-T

http://identifiers.org/hco/16/GRCh38#77806895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114947465-C-A

77806948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114947516-C-T

77807325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114949486-T-C

77807347-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114949514-T-A

77807483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114949791-G-A

77807483-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114949791-G-C

77807523-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114949829-C-G

http://identifiers.org/hco/16/GRCh38#77807561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114949866-C-A

77807561-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114949866-C-G

77807589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114949894-A-G

77807601-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114949903-G-C

77807748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114950045-G-A

http://identifiers.org/hco/16/GRCh38#77807824-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114950088-C-A

77807847-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114950115-G-C

77807978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114950230-C-T

http://identifiers.org/hco/16/GRCh38#77808961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114950355-C-A

77808981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114950375-T-C

77808982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114950376-A-G

77809237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114950583-G-A

77809314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114950669-G-A

77809388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114950756-T-C

77809469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114950965-T-C

77809470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114950966-C-T

77809481-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114950977-G-C

77809537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114951111-G-A

77809721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114951292-G-A

77809746-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114951319-C-G

77809795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114951368-G-A

77810089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114951661-T-C

77810215-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114951787-A-T

77810237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114951803-T-C

77810395-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114951916-T-A

77812711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114952406-A-G

77812848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114952541-T-C

77812896-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114952688-T-A

77812896-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114952688-T-G

77813147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114953065-G-A

77813339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114953186-G-A

77813352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114953196-G-A

77813369-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114953212-G-C

77813379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114953222-G-A

77813390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114953233-C-T

77813427-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114953270-C-G

77814189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114954552-G-A

77814201-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114954564-C-G

77814436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114954736-C-T

77814477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114954773-A-G

77814524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114954818-T-C

77814530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114954824-G-A

77814532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114954826-G-A

77814573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114954866-A-G

77814856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114955143-C-T

77815107-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114955379-A-T

77815360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114955616-A-G

77815417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114955681-T-C

77815421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114955685-G-A

77815432-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114955698-G-C

77815477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114955740-A-G

77815985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114956012-A-G

http://identifiers.org/hco/16/GRCh38#77816004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114956031-C-A

77816104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114956131-A-G

77816105-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114956132-A-T

77816124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114956148-C-T

77816707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114956722-G-T

77816823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114956845-G-A

77816823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114956845-G-T

77816824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114956846-G-A

77816824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114956846-G-T

77816851-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114956882-G-C

77816851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114956882-G-T

77817029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 114957054-G-A

77817054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114957079-A-G

77817082-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114957108-T-A

77817082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114957108-T-C

77817092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114957118-A-G

77817097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114957122-T-C

http://identifiers.org/hco/16/GRCh38#77817151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114957170-C-A

77817151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114957170-C-T

http://identifiers.org/hco/16/GRCh38#77817418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114957285-C-A

77817497-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114957359-T-A

77817865-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114957909-T-G

77818129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114958216-C-T

http://identifiers.org/hco/16/GRCh38#77818199-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114958292-A-C

77818241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114958334-C-T

http://identifiers.org/hco/16/GRCh38#77818434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114958794-C-A

77818467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114958824-C-T

77818626-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114958963-G-C

77818626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114958963-G-T

77818730-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114959066-A-T

77818755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114959092-T-C

77818755-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114959092-T-G

77818788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114959131-G-A

77818788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114959131-G-T

77818936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114959275-T-C

77818950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114959289-C-T

77818951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114959290-G-A

77819224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114959468-T-C

77819290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114959528-G-A

77819290-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114959528-G-C

77819299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114959537-G-T

77822641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114961410-G-A

77822673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114961444-A-G

77822721-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114961484-C-G

77822772-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114961527-C-G

77823489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114962138-A-G

77823527-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114962176-G-C

77823673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114962315-A-G

77825159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114963253-G-A

77825159-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114963253-G-C

77825202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114963296-G-A

77825202-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114963296-G-C

77825293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: synonymous variant
orthologous variants: 114963370-G-A

77825293-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: missense variant
orthologous variants: 114963370-G-C

77825374-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: missense variant
orthologous variants: 114963451-C-G

77825374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: synonymous variant
orthologous variants: 114963451-C-T

77825419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: synonymous variant
orthologous variants: 114963496-G-T

77825505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114963582-G-A

77825505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114963582-G-T

77825529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114963609-G-A

77825529-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114963609-G-T

77825539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114963619-G-A

http://identifiers.org/hco/16/GRCh38#77825564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114963644-C-A

77825572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114963653-T-C

http://identifiers.org/hco/16/GRCh38#77829264-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114964314-A-C

77829265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114964315-C-T

77829300-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114964347-T-A

77829379-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114964422-G-C

77829709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114964749-T-C

77829771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114964816-G-A

77829943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114964973-G-A

http://identifiers.org/hco/16/GRCh38#77830035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114965072-C-A

77830052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114965089-G-A

77830277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114965285-A-G

http://identifiers.org/hco/16/GRCh38#77830354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114965356-C-A

77830354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114965356-C-T

http://identifiers.org/hco/16/GRCh38#77831128-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114965482-A-C

77831276-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114965615-A-T

77831476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114965888-A-G

77831586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114965973-T-C

77832201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114966572-C-T

77832218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114966589-C-T

77832438-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114966770-A-T

77832552-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114966992-T-G

77832644-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114967183-T-G

77832668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114967269-A-G

http://identifiers.org/hco/16/GRCh38#77832785-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114967437-A-C

77833040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114968158-T-C

77833138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114968256-T-C

77833242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114968367-G-A

77833331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114968454-C-T

77833413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114968533-A-G

77833465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114968581-G-A

77833465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114968581-G-T

77833817-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114968612-G-C

77833817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114968612-G-T

77833839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114968634-G-A

77833915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, undefined
orthologous variants: 114968713-T-C

77834101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, undefined
orthologous variants: 114970516-G-A

77834602-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, undefined
orthologous variants: 114970915-C-G

77835018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114971331-A-G

77835115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114971406-G-A

77835115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114971406-G-T

77835339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114971598-A-G

77835924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114971859-T-C

77835926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114971861-G-A

77835927-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114971862-A-T

77836066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114971978-T-C

77836067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114971979-A-G

77836143-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114972068-G-C

77836322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114972227-G-T

77836334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114972239-G-A

77836362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114972268-A-G

77836441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114972347-T-C

77837096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114972910-G-A

77837473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114973162-A-G

77837551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114973232-G-A

http://identifiers.org/hco/16/GRCh38#77837605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114973294-C-A

77837732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114973398-T-C

http://identifiers.org/hco/16/GRCh38#77837787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114973454-C-A

77837792-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114973459-T-G

77837951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114973628-C-T

77838106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114973821-A-G

http://identifiers.org/hco/16/GRCh38#77838300-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114974007-A-C

http://identifiers.org/hco/16/GRCh38#77838344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114974052-C-A

77838344-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114974052-C-G

77838364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114974072-G-A

77838371-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114974079-C-G

77838392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114974100-A-G

77838544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114974253-G-A

http://identifiers.org/hco/16/GRCh38#77840582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114976603-C-A

77840609-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114976577-C-G

77840609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114976577-C-T

77840643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114976543-T-C

77840698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114976490-T-C

http://identifiers.org/hco/16/GRCh38#77840730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114976458-C-A

77840796-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114976401-A-T

77842194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114976916-G-A

77842321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114977030-G-A

77842321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114977030-G-T

77842414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114977118-G-A

77842553-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114977251-T-G

77842630-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114977325-C-G

77842636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114977332-G-A

77842643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114977339-G-A

77843352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114978291-C-T

77843510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114978445-G-A

77843623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114978557-A-G

77843623-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114978557-A-T

77843630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114978564-G-A

77844071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114978887-T-C

77844092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114978908-C-T

77844093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114978909-A-G

77844113-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114978928-T-G

http://identifiers.org/hco/16/GRCh38#77845170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114979800-C-A

http://identifiers.org/hco/16/GRCh38#77845179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114979808-C-A

77845271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114979902-T-C

77845421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114980046-A-G

http://identifiers.org/hco/16/GRCh38#77845480-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114980095-A-C

77845529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114980127-T-C

77845578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114980176-A-G

77845713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114980330-G-A

77846367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114981188-C-T

77846416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114981235-A-G

77846416-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114981235-A-T

77846569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114981829-A-G

77846569-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114981829-A-T

77846610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114981865-G-A

77846873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114982126-G-A

77846888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114982141-T-C

77846926-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114982166-G-C

77847160-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114982393-G-C

77847171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114982403-A-G

77847253-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114982474-T-A

77847744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114982989-G-A

77847751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114982996-T-C

http://identifiers.org/hco/16/GRCh38#77847887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114983116-C-A

77847887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114983116-C-T

77848369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114983548-C-T

77848710-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114983825-T-G

77848887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114983902-G-A

77849511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114984340-G-A

77849681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114984508-T-C

77849834-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114984657-G-T

http://identifiers.org/hco/16/GRCh38#77849838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114984661-C-A

77849838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114984661-C-T

77849864-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114984688-A-T

77849923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114984743-T-C

77850020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114984841-G-A

http://identifiers.org/hco/16/GRCh38#77850022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114984843-C-A

77850066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114984888-G-T

77850067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114984889-G-T

77850172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114984989-G-A

77850172-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114984989-G-C

77850203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114985020-G-A

77850215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114985031-A-G

77850311-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114985108-T-A

77850515-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114985307-C-G

77850888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114985641-T-C

77850935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114985706-G-T

77850944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114985715-C-T

77851160-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114985925-A-T

77851262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114986036-A-G

77851340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114986117-A-G

77853306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114989245-G-T

77853610-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114989745-C-G

77853668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114989800-A-G

77854488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114990606-G-A

77854609-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114990706-A-T

77854610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114990707-G-A

77854721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114990814-C-T

77854851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114990947-T-C

77856482-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114993154-A-T

77856526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114993185-C-T

http://identifiers.org/hco/16/GRCh38#77856578-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114993252-A-C

http://identifiers.org/hco/16/GRCh38#77856695-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114993365-A-C

77856736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114993401-C-T

77856945-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114993735-C-G

77857035-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114993815-G-C

http://identifiers.org/hco/16/GRCh38#77857173-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114993952-A-C

77857189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114993968-G-A

77857296-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114994078-T-A

77857296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114994078-T-C

77857360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114994142-G-A

77857364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114994146-T-C

77857364-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114994146-T-G

77859969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114995164-T-C

http://identifiers.org/hco/16/GRCh38#77860098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114995295-C-A

77860122-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114995319-T-G

77860197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114995380-G-A

77860282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114995462-C-T

77860298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114995478-C-T

77860348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114995530-C-T

77860670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114995752-C-T

77860697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114995783-C-T

77860797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114995879-C-T

77860859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114995935-A-G

77860876-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114995952-G-C

77860930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114996006-T-C

77860944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114996020-A-G

77860985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114996062-C-T

77861117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114996182-C-T

77861137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114996202-T-C

77861193-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114996257-T-G

77861284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114996402-C-T

http://identifiers.org/hco/16/GRCh38#77861599-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114996735-A-C

77861599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114996735-A-G

http://identifiers.org/hco/16/GRCh38#77861605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114996741-C-A

77861813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114996947-C-T

77861927-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114997021-G-C

77862654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114997853-A-G

77862654-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114997853-A-T

77862705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114997987-G-A

77862705-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114997987-G-C

77862709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114997991-G-A

77862709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114997991-G-T

77862711-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 114997993-T-A

http://identifiers.org/hco/16/GRCh38#77862981-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114998342-A-C

77862981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114998342-A-G

http://identifiers.org/hco/16/GRCh38#77862993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114998500-C-A

77862993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114998500-C-T

77862994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114998501-A-G

77863074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114998581-A-G

77863111-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114998625-T-G

77863265-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114998766-A-T

77863277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114998778-G-A

77863328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114998826-G-A

77863328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114998826-G-T

http://identifiers.org/hco/16/GRCh38#77863370-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#114998870-A-C

77863370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114998870-A-G

77863523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114999021-C-T

77863658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114999155-T-C

77864868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115000267-G-A

77864894-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115000291-T-G

77864895-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115000292-C-G

77864916-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115000312-T-G

77864927-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115000323-A-T

77864934-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115000330-C-G

77865690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115001325-T-C

77865830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115001449-T-C

77865843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115001464-G-A

77865880-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115001501-G-C

77865885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115001506-A-G

77866111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115001707-A-G

77866260-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115001853-A-T

77866303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115001895-T-C

77866305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115001897-G-A

77866344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115001934-G-T

77866396-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115002039-T-A

77866627-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115002267-A-T

77866856-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115002735-T-G

77867029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115002914-C-T

http://identifiers.org/hco/16/GRCh38#77867093-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115002989-A-C

77867093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115002989-A-G

77867134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115003032-T-C

77867210-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115003098-T-A

77867245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115003133-G-A

http://identifiers.org/hco/16/GRCh38#77868453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115003519-C-A

77868485-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115003549-C-G

77868588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115003655-G-A

77868596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115003662-G-A

77868596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115003662-G-T

77868637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115003700-C-T

77868651-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115003714-C-G

77868651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115003714-C-T

77868680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115003761-C-T

77868755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115003835-G-A

77868755-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115003835-G-C

http://identifiers.org/hco/16/GRCh38#77868896-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115003949-C-A

77868896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115003949-C-T

77868967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115004446-G-A

77868967-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115004446-G-C

77868967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115004446-G-T

77869085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115004548-T-C

77869807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115005516-C-T

77869808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115005517-G-A

77869816-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115005525-G-C

77869975-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115005675-A-T

77870061-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115005759-C-G

77870061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115005759-C-T

77870086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115005782-A-G

77870127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115005883-G-T

77870151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115005907-T-C

77870183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115005938-A-G

77870183-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115005938-A-T

http://identifiers.org/hco/16/GRCh38#77870321-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115006518-A-C

77870380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115006582-G-A

77870380-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115006582-G-C

http://identifiers.org/hco/16/GRCh38#77870497-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115006675-A-C

77870497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115006675-A-G

77870551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115006711-G-T

77870552-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115006712-G-C

http://identifiers.org/hco/16/GRCh38#77870561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115006721-C-A

77870599-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115006758-C-G

77870599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115006758-C-T

77870740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115006884-C-T

77870837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115006961-G-A

77870837-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115006961-G-C

77870940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115007085-C-T

77876292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115008909-T-C

77876300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115008917-G-T

77876539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115009152-G-A

77876539-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115009152-G-C

77876539-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115009152-G-T

77876558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115009171-G-T

http://identifiers.org/hco/16/GRCh38#77876625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115009251-C-A

77877572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115009614-G-A

77877572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115009614-G-T

http://identifiers.org/hco/16/GRCh38#77877584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115009626-C-A

77877673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115009711-A-G

77878302-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115010237-C-G

77878346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115010290-C-T

77878418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115010358-T-C

77878543-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115010463-C-G

77878543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115010463-C-T

77878585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115010534-A-G

77878893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115010807-C-T

http://identifiers.org/hco/16/GRCh38#77878904-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115010817-A-C

77878968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115010880-T-C

http://identifiers.org/hco/16/GRCh38#77879020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115010932-C-A

77879020-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115010932-C-G

77879020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115010932-C-T

77879060-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115010970-T-A

77879060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115010970-T-C

http://identifiers.org/hco/16/GRCh38#77879062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115010972-C-A

77879062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115010972-C-T

http://identifiers.org/hco/16/GRCh38#77879083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115010990-C-A

77879083-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115010990-C-G

77879083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115010990-C-T

77879126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115011031-T-C

http://identifiers.org/hco/16/GRCh38#77879131-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115011036-A-C

77879135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115011040-G-A

77879279-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115011179-A-T

77879607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115011350-C-T

77879617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115011360-A-G

77879630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115011374-A-G

77879642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115011386-A-G

77879654-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115011398-A-T

77879694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115011441-A-G

77879739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115011458-G-A

77879834-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115011861-G-C

77881287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115012747-G-T

http://identifiers.org/hco/16/GRCh38#77881606-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115013215-A-C

77881697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115013325-T-C

77881803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115013425-G-T

77881849-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115013471-G-C

77882078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115013699-T-C

77882343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115013948-A-G

http://identifiers.org/hco/16/GRCh38#77882368-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115013973-A-C

77882572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115014184-C-T

77882588-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115014200-G-C

77882588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115014200-G-T

77883800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115014770-C-T

http://identifiers.org/hco/16/GRCh38#77884464-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115015845-A-C

77884496-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115015876-G-C

77884496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115015876-G-T

77884546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115015926-T-C

77884567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115015947-G-A

77884567-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115015947-G-C

77884567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115015947-G-T

77884599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115015979-T-C

http://identifiers.org/hco/16/GRCh38#77884837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115016206-C-A

77884837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115016206-C-T

http://identifiers.org/hco/16/GRCh38#77884900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115016255-C-A

77884900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115016255-C-T

77884901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115016256-A-G

77884941-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115016478-T-G

77885028-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115016582-C-G

77885124-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115016681-A-T

77885206-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115016761-T-G

77885234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115016792-A-G

77885239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115016797-G-A

77885271-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115016812-G-C

77885282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115016823-G-A

77885343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115016912-C-T

77885344-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115016913-A-T

77885348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115016917-G-A

77885373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115016927-C-T

77885474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115017032-G-A

77885485-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115017043-G-C

77885485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115017043-G-T

77885525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115017082-G-A

http://identifiers.org/hco/16/GRCh38#77885665-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115017188-A-C

77886060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115017972-A-G

77886335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115018231-C-T

77886359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115018254-G-A

77886586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115018464-A-G

77886600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115018478-G-A

77886601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115018479-G-A

77886748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115018909-A-G

77886762-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115018940-A-T

77886767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115018945-C-T

77886770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115018948-T-C

77886782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115018954-G-A

77886782-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115018954-G-C

77886805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115018977-G-A

77886902-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115019066-T-A

77886990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115019148-C-T

77887087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115019232-A-G

http://identifiers.org/hco/16/GRCh38#77887403-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115019490-A-C

77887460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115019529-C-T

77887629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115019681-G-T

77887700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115019752-C-T

77887716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115019768-C-T

77887951-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115020438-C-G

77887971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115020458-C-T

77888473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115020883-G-T

77888589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115021262-C-T

77888608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115021281-T-C

77888647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115021317-C-T

77888823-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115021819-C-G

http://identifiers.org/hco/16/GRCh38#77889040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115022037-C-A

77889268-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115022272-C-G

77889391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115022405-T-C

77889789-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115023008-G-C

77891457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115025059-T-C

77891628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115025298-A-G

77891771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115025442-G-A

77891771-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115025442-G-C

77893461-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115025659-T-A

77893767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115026813-A-G

77893857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115026898-C-T

77893945-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115026991-A-T

77894323-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115027340-T-G

77894355-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115027373-G-C

77894478-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115027493-C-G

77894478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115027493-C-T

77894567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115027580-T-C

77894568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115027581-G-T

http://identifiers.org/hco/16/GRCh38#77894688-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115027714-A-C

77894689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115027715-A-G

http://identifiers.org/hco/16/GRCh38#77894747-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115027773-A-C

77894751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115027777-G-A

77894759-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115027785-A-T

77895328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115029106-G-T

77895358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115029134-C-T

77895653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115029478-C-T

77895720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115029549-G-A

77895789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115029611-C-T

77895874-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115029687-A-T

77895974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115029781-C-T

77896068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115029888-G-A

77896076-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115029895-G-C

77896252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115030046-C-T

77896404-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115030206-T-G

http://identifiers.org/hco/16/GRCh38#77896427-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115030232-A-C

77896428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115030233-C-T

77896693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115030438-G-A

77896693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115030438-G-T

77896712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115030457-A-G

77896712-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115030457-A-T

77897014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, undefined
orthologous variants: 115030746-T-C

77897122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115030861-A-G

77897263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, undefined
orthologous variants: 115031007-G-A

77897263-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, undefined
orthologous variants: 115031007-G-C

77897291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, undefined
orthologous variants: 115031037-G-A

77897720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115031566-C-T

77897722-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115031568-G-C

http://identifiers.org/hco/16/GRCh38#77897816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115031671-C-A

77897962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115031814-G-A

77897962-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115031814-G-C

77898322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115032144-A-G

77898328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115032710-G-A

77898328-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115032710-G-C

77898328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115032710-G-T

77898329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115032711-G-A

77898329-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115032711-G-C

77898329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115032711-G-T

77898373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115032742-G-A

77898373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115032742-G-T

77898412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115032770-A-G

77898479-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115032840-C-G

77898752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115033084-C-T

77899055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115033382-T-C

77899117-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115033441-C-G

77899117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115033441-C-T

77899381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115033963-G-T

77899451-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115034036-A-T

77899465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115034061-C-T

77899864-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115034682-G-C

77899871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115034689-C-T

77899900-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115034719-T-A

77899914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115034733-T-C

77899932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115034749-A-G

77899937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115034754-A-G

77899971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115034787-T-C

http://identifiers.org/hco/16/GRCh38#77899987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115034802-C-A

77899987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115034802-C-T

77900014-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115034827-C-G

77900775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115035804-G-A

77900867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115035889-C-T

77901001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115036003-G-A

77901026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115036043-A-G

77901030-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115036047-C-G

77901050-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115036065-G-C

77901453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115036148-C-T

77901480-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115036176-G-C

77901563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115036273-G-A

77901563-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115036273-G-C

http://identifiers.org/hco/16/GRCh38#77901635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115036346-C-A

77901635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115036346-C-T

77901638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115036349-G-A

77901674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115036421-T-C

77901729-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115036494-C-G

77901757-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115036528-A-T

http://identifiers.org/hco/16/GRCh38#77902180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115036748-C-A

77902180-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115036748-C-G

77902186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115036754-T-C

77902238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115036803-A-G

77902464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115037006-G-T

77902698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115037205-G-A

77902967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115037406-T-C

77902984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115037423-A-G

77902991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115037435-G-A

77902991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115037435-G-T

http://identifiers.org/hco/16/GRCh38#77903191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115037546-C-A

77903204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115037559-A-G

77903218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115037573-G-A

77903337-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115037693-T-A

77903438-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115037793-G-C

77903438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115037793-G-T

77903555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115037909-G-A

77903555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115037909-G-T

77903637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115037992-G-A

77903637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115037992-G-T

77904215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115038591-A-G

77904215-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115038591-A-T

77904247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115038686-G-T

77904258-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115038697-T-G

77904381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115038828-C-T

http://identifiers.org/hco/16/GRCh38#77904484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115038934-C-A

77904589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115039055-A-G

77904598-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115039064-C-G

77904798-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115039313-T-G

77904857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115039366-C-T

77904860-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115039369-T-G

77904892-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115039403-C-G

http://identifiers.org/hco/16/GRCh38#77905321-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115039826-A-C

77905574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115040043-C-T

77905579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115040048-T-C

77905640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115040097-G-A

77905791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115040228-G-A

77905987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115041132-G-A

77906003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115041148-G-A

77906003-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115041148-G-T

http://identifiers.org/hco/16/GRCh38#77906033-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115041178-A-C

77906317-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115041473-G-C

77906317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115041473-G-T

77906426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115041574-T-C

77906435-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115041583-T-A

77906500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115041644-C-T

77906682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115041819-G-T

77906736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115041870-A-G

http://identifiers.org/hco/16/GRCh38#77906828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115041946-C-A

http://identifiers.org/hco/16/GRCh38#77906908-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115042049-A-C

77906923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115042060-A-G

77906992-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115042111-T-G

77906994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115042113-G-A

77907007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115042126-A-G

http://identifiers.org/hco/16/GRCh38#77907029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115042148-C-A

77907119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115042220-A-G

77907127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115042228-A-G

77907226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115042303-G-A

77907226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115042303-G-T

77907306-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115042382-C-G

77907316-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115042391-C-G

77907316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115042391-C-T

http://identifiers.org/hco/16/GRCh38#77907452-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115043221-A-C

77907527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115043296-C-T

77907615-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115043368-G-C

77907668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115043427-C-T

77907669-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115043428-A-T

77907699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115043458-C-T

http://identifiers.org/hco/16/GRCh38#77907784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115043531-C-A

77907784-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115043531-C-G

77907795-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115043542-C-G

77907795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115043542-C-T

77907818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115043565-A-G

77907818-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115043565-A-T

77907832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115043579-C-T

77913910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115044217-G-A

77913910-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115044217-G-C

77913925-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115044232-G-C

77913927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115044237-G-A

77913927-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115044237-G-C

77913934-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115044244-T-G

77913948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115044258-C-T

77913969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115044279-A-G

77914109-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115044419-G-C

http://identifiers.org/hco/16/GRCh38#77914144-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115044452-A-C

77914349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115044661-G-A

http://identifiers.org/hco/16/GRCh38#77917095-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115046656-A-C

77917152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115046712-T-C

77917327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115046877-A-G

77917357-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115046907-A-T

77917518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115047072-A-G

77917678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115047230-A-G

77917689-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115047237-C-G

77917942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115048114-G-T

77918078-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115048653-C-G

77918079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115048654-A-G

77918134-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115048702-G-C

77918165-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115048731-G-T

77918246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115048810-G-T

77918457-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115049021-C-G

77918549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115049110-G-A

77918570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115049131-T-C

77918631-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115049203-A-T

77918730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115049297-A-G

77918730-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115049297-A-T

77918739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115049305-T-C

http://identifiers.org/hco/16/GRCh38#77918758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115049327-C-A

77918916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115049542-T-C

77918960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115049596-C-T

77919042-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115049688-G-C

77919057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115049707-G-T

77919349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115049995-G-T

http://identifiers.org/hco/16/GRCh38#77919439-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115050085-A-C

77919486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115050126-C-T

77919508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115050154-A-G

77919520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115050176-G-A

77919573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115050229-T-C

77919675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115050308-C-T

77922235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115058631-C-T

77922406-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115058802-G-C

77922479-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115058873-G-C

77922530-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115058924-G-C

77922559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115058959-G-A

77922559-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115058959-G-C

77922605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115059004-G-A

77922646-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115059047-G-C

77922838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115059237-G-A

77922883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115059276-C-T

77922971-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115059369-C-G

77922974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115059372-G-A

77923176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115059504-C-T

77923379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115059556-G-A

77923576-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115059698-G-C

http://identifiers.org/hco/16/GRCh38#77923733-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115059853-A-C

77923875-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115059954-G-C

77923899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115059978-A-G

http://identifiers.org/hco/16/GRCh38#77923954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115060030-C-A

77923954-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115060030-C-G

77923954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115060030-C-T

77924068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115060143-T-C

77924072-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115060145-A-T

77924301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115060369-C-T

77924374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115060442-T-C

77925415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115060913-C-T

77925449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115060946-T-C

77925454-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115060951-A-T

77925465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115060960-G-A

77925512-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115060987-G-C

77925566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115061044-G-A

77925618-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115061096-G-C

http://identifiers.org/hco/16/GRCh38#77925810-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115061304-A-C

77925823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115061316-A-G

77926604-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115062050-A-T

77926795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115062284-A-G

77928613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115062364-T-C

77928732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115062490-T-C

77928771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115062529-T-C

77928782-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115062540-G-C

77929257-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115062700-T-G

77929296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115062739-G-T

77929297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115062740-G-A

77929406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115062825-G-A

http://identifiers.org/hco/16/GRCh38#77929597-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115063019-A-C

77929828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115063221-A-G

77930020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115063321-T-C

77930208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115063453-T-C

77930208-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115063453-T-G

77930235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115063480-C-T

77930246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115063491-A-G

77930317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115063656-G-A

77930336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115063673-T-C

http://identifiers.org/hco/16/GRCh38#77930505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115063838-C-A

77930704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115064032-A-G

77930755-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115064092-G-C

77930807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115064148-G-T

77931056-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115064376-T-G

77931196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115064497-C-T

77931236-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115064533-T-A

77931236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115064533-T-C

77931247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115064544-G-A

77931247-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115064544-G-C

77931598-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115065139-C-G

77931659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115065210-G-T

77931664-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115065215-G-C

http://identifiers.org/hco/16/GRCh38#77931783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115065330-C-A

77931783-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115065330-C-G

77931783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115065330-C-T

77932370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115065791-G-A

77932393-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115065809-C-G

77932396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115065812-C-T

77932873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115066175-A-G

77933047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115066283-G-A

http://identifiers.org/hco/16/GRCh38#77933212-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115066371-A-C

77933306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115066473-G-A

http://identifiers.org/hco/16/GRCh38#77933307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115066474-C-A

77933342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115066501-C-T

77933410-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115066570-T-A

77933420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115066580-C-T

http://identifiers.org/hco/16/GRCh38#77933439-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115066600-A-C

77933439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115066600-A-G

77933478-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115066639-G-C

77933534-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115066694-C-G

77933586-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115066758-T-A

77933586-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115066758-T-G

77933598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115066769-G-A

77933598-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115066769-G-C

77933692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115066839-G-T

77933703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115066856-A-G

77933706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115066859-G-A

77933706-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115066859-G-C

77933727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115066877-C-T

77933752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115066902-A-G

77933972-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115067097-C-G

77933972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115067097-C-T

77933973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115067098-G-A

77934047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115067201-G-A

77934082-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115067236-G-C

77934311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115067445-A-G

77934314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115067448-C-T

77934321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115067450-G-A

77934628-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115067805-G-C

77934740-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115067905-C-G

77934755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115067920-G-A

77934880-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115068043-G-C

77935025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115068177-C-T

77935026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115068178-G-A

77935115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115068258-T-C

http://identifiers.org/hco/16/GRCh38#77935167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115068310-C-A

77935167-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 115068310-C-G

77935221-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115068370-G-C

77935336-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115068481-T-A

http://identifiers.org/hco/16/GRCh38#77935475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115068617-C-A

http://identifiers.org/hco/16/GRCh38#77935516-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115068650-A-C

http://identifiers.org/hco/16/GRCh38#77939109-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115070603-A-C

77939151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115070641-G-A

77939186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115070676-A-G

77939342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115070806-A-G

77939358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115070809-A-G

77939359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115070810-T-C

77939380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115070821-G-A

77939439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115070860-A-G

77939467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115070888-C-T

77939794-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115071637-C-G

77940060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115071912-T-C

77940097-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115071953-T-A

77940097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115071953-T-C

77940116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115071964-T-C

77940308-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115072138-C-G

77940330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115072159-A-G

77944505-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115072685-C-G

77944515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115072695-G-A

http://identifiers.org/hco/16/GRCh38#77944724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115072886-C-A

77944805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115072957-T-C

77944841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115072990-G-A

http://identifiers.org/hco/16/GRCh38#77944990-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115073398-A-C

77945014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115073422-G-A

77945131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115073525-G-A

77946761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115077982-G-A

77946812-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115078039-G-C

77946823-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115078051-C-G

77946958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115078168-C-T

77946990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115078200-G-A

77946996-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115078206-A-T

77947002-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115078212-T-A

77947081-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115078289-G-C

77947116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115078359-G-A

77947350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115078580-A-G

http://identifiers.org/hco/16/GRCh38#77947406-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115078623-A-C

77947587-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115078755-C-G

77947587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115078755-C-T

http://identifiers.org/hco/16/GRCh38#77947632-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115078801-A-C

77947632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115078801-A-G

http://identifiers.org/hco/16/GRCh38#77947634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115078803-C-A

77947688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115078853-G-A

77947726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115078881-T-C

77947729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115078884-A-G

http://identifiers.org/hco/16/GRCh38#77948232-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115079094-A-C

77948411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115079263-A-G

77948444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115079276-G-A

http://identifiers.org/hco/16/GRCh38#77948852-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115079912-A-C

77953520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115080606-A-G

77953540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115080629-G-T

77953541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115080630-G-A

77953541-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115080630-G-C

77953802-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115080842-G-C

77953887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115080924-C-T

77953938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115080974-T-C

http://identifiers.org/hco/16/GRCh38#77954099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115081137-C-A

77954251-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115081283-G-C

77954254-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115081286-G-C

77954269-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115081301-T-G

77956524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115082816-A-G

77956546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115082840-G-A

77956832-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115083072-T-A

77956996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115083159-C-T

77956997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115083160-C-T

77957085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115083183-G-A

77957085-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115083183-G-C

77957085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115083183-G-T

http://identifiers.org/hco/16/GRCh38#77957113-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115083205-A-C

77957245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115083944-G-A

77958710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115084042-G-A

77958710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115084042-G-T

http://identifiers.org/hco/16/GRCh38#77958781-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115084108-A-C

http://identifiers.org/hco/16/GRCh38#77958851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115084180-C-A

77959075-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115084634-G-C

77959181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115084712-G-T

77959185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115084716-T-C

http://identifiers.org/hco/16/GRCh38#77959195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115084726-C-A

77959195-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115084726-C-G

77959367-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115085099-C-G

77959495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115085222-G-T

77959769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115085500-G-T

77960570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115087248-A-G

77960581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115087259-T-C

77960824-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115087444-G-C

77960916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115087530-C-T

77961098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115087700-T-C

77961132-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115087728-G-C

77961199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115087798-C-T

77961204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115087803-A-G

77961389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115087962-A-G

77961404-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115087999-T-G

77961472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115088066-G-A

77962055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115088275-A-G

77962312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115088507-G-A

77962363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115088550-C-T

77962404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115088592-A-G

http://identifiers.org/hco/16/GRCh38#77962411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115088598-C-A

77962477-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115088631-C-G

77962477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115088631-C-T

77962518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115088665-C-T

77962531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115088678-C-T

77962638-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-T

http://identifiers.org/hco/16/GRCh38#77962948-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115088919-A-C

http://identifiers.org/hco/16/GRCh38#77962956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115088927-C-A

77963166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115089186-C-T

77963229-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115089249-G-C

77963236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115089256-C-T

77963298-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115089350-G-C

77963298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115089350-G-T

77963325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115089374-A-G

77963429-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115089478-C-G

77963508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115089557-T-C

77963725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115089732-G-T

77963752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115089759-C-T

77963778-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115089780-C-G

77965127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115089970-T-C

77965139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115089982-C-T

http://identifiers.org/hco/16/GRCh38#77965262-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115090221-A-C

77965510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115090418-C-T

http://identifiers.org/hco/16/GRCh38#77965654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115090597-C-A

77965878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115090819-A-G

77966038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115091290-C-T

77966082-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115091329-T-A

77966082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115091329-T-C

77966114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115091372-G-T

77966185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115091444-G-A

http://identifiers.org/hco/16/GRCh38#77966268-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115091522-C-A

http://identifiers.org/hco/16/GRCh38#77966360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115091625-C-A

77966365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115091630-A-G

http://identifiers.org/hco/16/GRCh38#77966420-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115091673-A-C

77966697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115091962-A-G

77966798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115092334-G-A

http://identifiers.org/hco/16/GRCh38#77966816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115092347-C-A

77966816-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115092347-C-G

77966857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115092389-A-G

77966877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115092409-T-C

77966877-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115092409-T-G

77966983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115092495-G-A

http://identifiers.org/hco/16/GRCh38#77967440-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115092874-A-C

77967441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115092875-A-G

77967441-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115092875-A-T

77967508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115092951-A-G

http://identifiers.org/hco/16/GRCh38#77967753-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115093210-C-A

77969890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

77969890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-T

77969916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-C

77970285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115095147-T-C

77970305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115095173-A-G

77970861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115095718-A-G

77971128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115095947-C-T

77971230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 115096037-G-A

77971382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115096198-G-A

77971382-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115096198-G-C

77971382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115096198-G-T

77971384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115096200-G-A

77971419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115096235-T-C

77971473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115096291-G-A

77971638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115096401-G-A

77971638-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115096401-G-C

77971644-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115096407-G-C

77971680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115096448-C-T

77971743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115096503-G-A

77971743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115096503-G-T

http://identifiers.org/hco/16/GRCh38#77971744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#115096504-C-A

77971744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, undefined
orthologous variants: 115096504-C-T

77971762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, undefined
orthologous variants: 115096522-A-G

77971765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, undefined
orthologous variants: 115096525-T-C

http://identifiers.org/hco/16/GRCh38#77971783-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#115096543-A-C

77971783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, undefined
orthologous variants: 115096543-A-G

http://identifiers.org/hco/16/GRCh38#77971798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115096555-C-A

77971798-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115096555-C-G

77971798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115096555-C-T

http://identifiers.org/hco/16/GRCh38#77971809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115096560-C-A

77971809-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115096560-C-G

77971809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115096560-C-T

http://identifiers.org/hco/16/GRCh38#77971876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115096618-C-A

http://identifiers.org/hco/16/GRCh38#77971894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115096636-C-A

77971894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: synonymous variant
orthologous variants: 115096636-C-T

http://identifiers.org/hco/16/GRCh38#77971989-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#115096732-A-C

77972007-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, undefined
orthologous variants: 115096750-G-C

77972007-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, undefined
orthologous variants: 115096750-G-T

77972039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, undefined
orthologous variants: 115096782-G-A

77972039-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, undefined
orthologous variants: 115096782-G-C

77972039-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, undefined
orthologous variants: 115096782-G-T

http://identifiers.org/hco/16/GRCh38#77972229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115096955-C-A

77972261-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, undefined
orthologous variants: 115096983-T-G

77972265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, undefined
orthologous variants: 115096987-A-G

77974863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115097920-C-T

77974892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115097948-G-A

http://identifiers.org/hco/16/GRCh38#77974904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115097960-C-A

77974904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115097960-C-T

77975020-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, undefined
orthologous variants: 115098076-G-C

77975085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron_variant, undefined
orthologous variants: 115098142-A-G

77977544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: intron variant
orthologous variants: 115098333-G-A

77977711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: 115098501-G-A

77977756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: 115098544-A-G

77977795-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: 115098583-T-A

77977909-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: 115098701-A-T

77977928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: 115098720-G-A

77977928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: 115098720-G-T

77977948-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: 115098740-T-A

http://identifiers.org/hco/16/GRCh38#77977998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115098792-C-A

http://identifiers.org/hco/16/GRCh38#77978006-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115098800-A-C

77978006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: 115098800-A-G

77978006-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: 115098800-A-T

77978007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: 115098801-T-C

77978007-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: 115098801-T-G

77978187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: 115098971-T-C

77978187-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: 115098971-T-G

http://identifiers.org/hco/16/GRCh38#77978212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115098995-C-A

77978212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: 115098995-C-T

77978260-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: 115099041-G-C

77978303-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: 115099087-A-T

77978330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: 115099114-G-A

77978330-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: 115099114-G-C

77978349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: 115099133-C-T

77978375-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: 115099160-G-C

http://identifiers.org/hco/16/GRCh38#77978384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115099169-C-A

77978384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: 115099169-C-T

77978432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: 115099218-T-C

77978525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: 115099277-G-A

77978525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: 115099277-G-T

77978570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: 115099310-G-T

77978631-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: 115099376-G-C

77978639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: 115099384-G-T

77978682-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: 115099427-T-A

http://identifiers.org/hco/16/GRCh38#77978792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115099525-C-A

77978820-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: 115099553-T-G

77978869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: 115099601-T-C

http://identifiers.org/hco/16/GRCh38#77978905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115099634-C-A

77978905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: 115099634-C-T

http://identifiers.org/hco/16/GRCh38#77978965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115099720-C-A

77979014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: 115099776-T-C

77979028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: 115099790-A-G

http://identifiers.org/hco/16/GRCh38#77979064-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115099887-C-A

77979086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: 115099905-C-T

http://identifiers.org/hco/16/GRCh38#77979098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115099917-C-A

77979098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: 115099917-C-T

77979103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: 115099922-G-T

http://identifiers.org/hco/16/GRCh38#77979165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115099983-C-A

77979176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: 115099994-G-A

77979176-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: 115099994-G-C

77979176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: 115099994-G-T

77979248-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: 115100072-A-T

77979291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: 115100115-T-C

77979295-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: 115100119-T-G

http://identifiers.org/hco/16/GRCh38#77979323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115100147-C-A

77979329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: 115100153-A-G

http://identifiers.org/hco/16/GRCh38#77979378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115100176-C-A

77979380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: 115100178-G-A

77979380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: 115100178-G-T

77979478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: 115100242-G-A

77979530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: 115100289-G-T

http://identifiers.org/hco/16/GRCh38#77979543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115100302-C-A

77979642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: 115100386-A-G

77979642-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: 115100386-A-T

77979846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: 115100549-G-A

77979846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: 115100549-G-T

77979933-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: 115100638-C-G

77979933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: 115100638-C-T

http://identifiers.org/hco/16/GRCh38#77979962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115100667-C-A

http://identifiers.org/hco/16/GRCh38#77979976-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#115100681-A-C

77979976-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: 115100681-A-T

77979990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: 115100695-T-C

77979990-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29315
most severe consequence: 3 prime UTR variant
orthologous variants: 115100695-T-G