89575527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 79310028-G-A

89575527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 79310028-G-T

http://identifiers.org/hco/15/GRCh38#89575533-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#79310039-A-C

89575533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 79310039-A-G

89575554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 79310060-G-A

89575554-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 79310060-G-C

89575554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 79310060-G-T

89575628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 79310129-G-A

89575628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 79310129-G-T

89575639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 79310140-C-T

http://identifiers.org/hco/15/GRCh38#89575799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#79310300-C-A

89575799-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 79310300-C-G

89575799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 79310300-C-T

http://identifiers.org/hco/15/GRCh38#89575859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#79310369-C-A

89575859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 79310369-C-T

http://identifiers.org/hco/15/GRCh38#89575862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#79310372-C-A

89575862-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 79310372-C-G

89575862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 79310372-C-T

89575874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 79310384-G-A

89575874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 79310384-G-T

89575943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 79310453-G-A

89575943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 79310453-G-T

http://identifiers.org/hco/15/GRCh38#89575983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#79310493-C-A

89575983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 79310493-C-T

89575985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 79310495-G-A

89575985-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 79310495-G-C

89575985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 79310495-G-T

http://identifiers.org/hco/15/GRCh38#89576045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#79310555-C-A

89576045-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 79310555-C-G

89576045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 79310555-C-T

89576069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 79310579-G-A

89576069-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 79310579-G-C

89576069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 79310579-G-T

89576114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 79310624-C-T

89576231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 79310741-A-G

89576233-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 79310743-G-C

http://identifiers.org/hco/15/GRCh38#89576349-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#79310839-A-C

89576349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: 79310839-A-G

89576351-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: 79310841-T-A

89576351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: 79310841-T-C

89576351-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: 79310841-T-G

89576361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: 79310851-T-C

89576361-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: 79310851-T-G

http://identifiers.org/hco/15/GRCh38#89576487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#79310995-C-A

89576487-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: 79310995-C-G

89576487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: 79310995-C-T

89576585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: 79311090-C-T

89576655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: 79311203-C-T

89580454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: 79313378-A-G

89581631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: 79314272-G-T

89582122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: 79314703-G-A

http://identifiers.org/hco/15/GRCh38#89582126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#79314707-C-A

89582126-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: 79314707-C-G

89582126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: 79314707-C-T

89582150-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: 79314730-C-G

89582150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: 79314730-C-T

89582188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: 79314764-G-A

89582188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: 79314764-G-T

89582640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: 79315369-A-G

89582680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 79315405-T-C

89582736-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 79315461-C-G

89582984-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: 79315709-A-T

89583001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: 79315903-A-G

89583001-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: 79315903-A-T

http://identifiers.org/hco/15/GRCh38#89583022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#79315919-C-A

89583022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: 79315919-C-T

89583205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: 79316097-G-T

http://identifiers.org/hco/15/GRCh38#89583265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#79316158-C-A

89583265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: 79316158-C-T

89583513-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: 79316385-T-A

89583599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: 79316505-A-G

89584015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: 79317202-A-G

http://identifiers.org/hco/15/GRCh38#89584069-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#79317224-A-C

89584153-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: 79317312-A-T

89584434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 79317553-C-T

89584463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 79317582-C-T

89584563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: 79317677-A-G

89584664-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: 79317787-T-G

89584757-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: 79318068-G-C

89584889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: 79318188-A-G

http://identifiers.org/hco/15/GRCh38#89584993-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#79318235-A-C

89585169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: 79318540-G-A

89585169-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: 79318540-G-C

89585632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: 79319123-T-C

89585685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: 79319174-A-G

89585746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 79319234-C-T

89585836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 79319324-A-G

http://identifiers.org/hco/15/GRCh38#89585955-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#79319443-A-C

89585975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: 79319463-A-G

http://identifiers.org/hco/15/GRCh38#89586079-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#79319563-C-A

89586079-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: 79319563-C-G

89586158-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: 79319634-C-G

89586158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: 79319634-C-T

89591452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: 79319975-A-G

89591474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: 79319997-A-G

89591499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 79320021-G-A

89591499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 79320021-G-T

http://identifiers.org/hco/15/GRCh38#89591533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#79320046-C-A

89591549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: 79320062-G-A

89591549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: 79320062-G-T

89591559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: 79320082-G-A

89591559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: 79320082-G-T

http://identifiers.org/hco/15/GRCh38#89591597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#79320111-C-A

89591597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: 79320111-C-T

89591609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: 79320123-A-G

89591677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: 79320219-G-T

89591678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: 79320220-A-G

http://identifiers.org/hco/15/GRCh38#89591680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#79320222-C-A

89591680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: 79320222-C-T

89591698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: 79320266-A-G

89591698-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: 79320266-A-T

89591724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: 79320294-C-T

89591746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: 79320338-T-C

89591845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: 79320438-G-A

89591845-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: 79320438-G-C

89591845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: 79320438-G-T

89591897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: 79320490-T-C

89591897-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, undefined
orthologous variants: 79320490-T-G

89591989-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron variant
orthologous variants: 79320572-T-A

89591989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron variant
orthologous variants: 79320572-T-C

89591989-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron variant
orthologous variants: 79320572-T-G

89592024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron variant
orthologous variants: 79320598-C-T

89594460-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: synonymous variant
orthologous variants: 79325065-T-A

89594460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: synonymous variant
orthologous variants: 79325065-T-C

89595184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron variant
orthologous variants: 79326779-G-T

89595400-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: synonymous variant
orthologous variants: 79326982-C-G

89595400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: synonymous variant
orthologous variants: 79326982-C-T

89595412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: synonymous variant
orthologous variants: 79326994-A-G

89595418-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: missense variant
orthologous variants: 79327000-A-T

89599120-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron variant
orthologous variants: 79328590-A-T

http://identifiers.org/hco/15/GRCh38#89599186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79328643-C-A

89599186-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron variant
orthologous variants: 79328643-C-G

89599334-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: synonymous variant
orthologous variants: 79328773-T-A

89599519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron variant
orthologous variants: 79328954-T-C

89600181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron variant
orthologous variants: 79329948-C-T

89600496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron variant
orthologous variants: 79330581-G-T

http://identifiers.org/hco/15/GRCh38#89600507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79330592-C-A

89600507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron variant
orthologous variants: 79330592-C-T

http://identifiers.org/hco/15/GRCh38#89600562-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79330634-A-C

89600562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron variant
orthologous variants: 79330634-A-G

89600562-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron variant
orthologous variants: 79330634-A-T

89600651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: missense variant
orthologous variants: 79330722-G-A

89600651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: stop gained
orthologous variants: 79330722-G-T

89600676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: missense variant
orthologous variants: 79330747-A-G

89600676-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: missense variant
orthologous variants: 79330747-A-T

89600725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron variant
orthologous variants: 79330794-A-G

89600725-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron variant
orthologous variants: 79330794-A-T

89600731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron variant
orthologous variants: 79330800-G-A

89600731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron variant
orthologous variants: 79330800-G-T

89601201-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron variant
orthologous variants: 79331460-T-G

89601214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron variant
orthologous variants: 79331476-T-C

89601217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron variant
orthologous variants: 79331479-A-G

89601229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron variant
orthologous variants: 79331491-G-T

http://identifiers.org/hco/15/GRCh38#89601234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79331496-C-A

89601234-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron variant
orthologous variants: 79331496-C-G

89601234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron variant
orthologous variants: 79331496-C-T

89601257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron variant
orthologous variants: 79331517-A-G

89601257-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron variant
orthologous variants: 79331517-A-T

89601292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 79331552-C-T

http://identifiers.org/hco/15/GRCh38#89601359-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79331619-A-C

89601359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: missense variant
orthologous variants: 79331619-A-G

89601421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron variant
orthologous variants: 79331677-A-G

89601591-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron variant
orthologous variants: 79331840-T-G

89601604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron variant
orthologous variants: 79331882-G-A

89601604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron variant
orthologous variants: 79331882-G-T

http://identifiers.org/hco/15/GRCh38#89601617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79331900-C-A

89602043-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron variant
orthologous variants: 79332288-C-G

89602518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron variant
orthologous variants: 79332449-T-C

89602694-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron variant
orthologous variants: 79332610-T-G

89602733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron variant
orthologous variants: 79332642-C-T

89602734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron variant
orthologous variants: 79332643-A-G

89606504-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron variant
orthologous variants: 79333728-C-G

89606677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron variant
orthologous variants: 79333869-A-G

89606710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron variant
orthologous variants: 79333901-T-C

89606726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron variant
orthologous variants: 79333918-A-G

http://identifiers.org/hco/15/GRCh38#89606955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79334113-C-A

89607085-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron variant
orthologous variants: 79334249-G-C

89608572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron variant
orthologous variants: 79335302-C-T

http://identifiers.org/hco/15/GRCh38#89608584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79335314-C-A

89608584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron variant
orthologous variants: 79335314-C-T

89608685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron variant
orthologous variants: 79335412-T-C

http://identifiers.org/hco/15/GRCh38#89608701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79335423-C-A

89608701-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron variant
orthologous variants: 79335423-C-G

89608701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron variant
orthologous variants: 79335423-C-T

http://identifiers.org/hco/15/GRCh38#89608711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79335433-C-A

89608711-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron variant
orthologous variants: 79335433-C-G

89608758-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron variant
orthologous variants: 79335486-T-A

89608758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: intron variant
orthologous variants: 79335486-T-C

89608976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 79335698-A-G

89609029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79335752-G-A

89609029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79335752-G-T

http://identifiers.org/hco/15/GRCh38#89609049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79335771-C-A

89609049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79335771-C-T

http://identifiers.org/hco/15/GRCh38#89616318-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79337890-A-C

89616318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79337890-A-G

89616326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79337898-A-G

89616527-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79338095-A-T

89616549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79338148-G-A

89616549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79338148-G-T

http://identifiers.org/hco/15/GRCh38#89616565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79338164-C-A

89616565-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79338164-C-G

89616627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79338251-T-C

89616628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79338252-C-T

89617030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79338718-G-A

89617312-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79338906-G-C

89617703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79339219-T-C

http://identifiers.org/hco/15/GRCh38#89618265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79339757-C-A

89618265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79339757-C-T

89618482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79339961-A-G

89619648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79340560-A-G

89619648-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79340560-A-T

89621384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79341562-G-A

89621384-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79341562-G-C

http://identifiers.org/hco/15/GRCh38#89621394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79341571-C-A

89621394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant, synonymous_variant
orthologous variants: 79341571-C-T

89621674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79342019-G-A

89621677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79342022-G-A

89621677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79342022-G-T

89621726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79342071-C-T

89621820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79342154-A-G

http://identifiers.org/hco/15/GRCh38#89622067-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79342262-A-C

89622330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79342337-A-G

89622469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79342406-C-T

89622650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79342559-C-T

89622694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79342617-C-T

89622701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79342624-C-T

89622855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79342852-G-A

89622872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79342872-A-G

89622946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79342994-G-A

89623178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79343219-C-T

89623492-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79343309-T-G

http://identifiers.org/hco/15/GRCh38#89623512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79343328-C-A

89623578-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79343407-T-A

89623578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79343407-T-C

89623578-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79343407-T-G

89623579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79343408-G-A

89623579-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79343408-G-C

89623579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79343408-G-T

89623704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 79343530-T-C

89624090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 79343916-G-A

89624090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 79343916-G-T

89624251-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 79344062-C-G

89624251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 79344062-C-T

89624426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 79344231-C-T

89624572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 79344377-G-A

89624572-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 79344377-G-C

89624798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 79344588-T-C

89624835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 79344628-T-C

89624970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 79344751-G-A

89624970-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 79344751-G-C

89625100-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 79344878-G-C

http://identifiers.org/hco/15/GRCh38#89625266-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79345044-C-A

89625266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 79345044-C-T

89625275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 79345053-T-C

89625603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 79345387-T-C

89625603-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 79345387-T-G

89625744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 79345528-T-C

http://identifiers.org/hco/15/GRCh38#89625844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79345611-C-A

http://identifiers.org/hco/15/GRCh38#89625911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79345658-C-A

89625911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79345658-C-T

89625917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79345664-C-T

89625998-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 79345745-C-G

89626077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79345827-G-A

http://identifiers.org/hco/15/GRCh38#89626162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79345872-C-A

89626162-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79345872-C-G

89626162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79345872-C-T

http://identifiers.org/hco/15/GRCh38#89626197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79345906-C-A

89626198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79345907-A-G

89626226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79345933-A-G

89626282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79345983-G-A

89626306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79345996-C-T

89626369-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79346033-A-T

89626480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79346112-G-A

89626665-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79346254-C-G

89626981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 79346427-C-T

89626987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 79346433-A-G

89627072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 79346566-C-T

89627286-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79347011-G-C

89627286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79347011-G-T

89627309-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79347026-G-C

89627385-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79347070-C-G

89627488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79347177-G-A

http://identifiers.org/hco/15/GRCh38#89627985-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79347726-A-C

89627985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79347726-A-G

http://identifiers.org/hco/15/GRCh38#89628084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#79347966-C-A

89628084-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79347966-C-G

89628084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79347966-C-T

89628090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79347972-G-A

89628090-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79347972-G-C

89628090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79347972-G-T

89628180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79348047-C-T

http://identifiers.org/hco/15/GRCh38#89628193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#79348060-C-A

89628269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79348154-G-A

89628269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79348154-G-T

89628308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79348193-G-T

89628713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 79348587-G-A

89628713-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 79348587-G-C

89628713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 79348587-G-T

89628814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79348685-C-T

89628833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79348708-C-T

89628953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79348886-T-C

89628978-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, splice_region_variant, undefined
orthologous variants: 79348900-C-G

89628992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 79348914-A-G

89629210-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79349110-T-A

89629210-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79349110-T-G

89629211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79349111-G-A

89629211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79349111-G-T

89629218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79349118-G-A

89629218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79349118-G-T

89629378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant, stop_gained, undefined
orthologous variants: 79349138-G-A

89629378-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 79349138-G-C

89629378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 79349138-G-T

89629400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 79349160-C-T

89629495-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant, undefined
orthologous variants: 79349255-T-G

89629508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant, undefined
orthologous variants: 79349268-C-T

89629522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, undefined
orthologous variants: 79349282-G-T

http://identifiers.org/hco/15/GRCh38#89629526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#79349286-C-A

89629526-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant, undefined
orthologous variants: 79349286-C-G

89629526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant, undefined
orthologous variants: 79349286-C-T

89629640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79349397-A-G

http://identifiers.org/hco/15/GRCh38#89629711-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#79349448-A-C

89629711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79349448-A-G

89629711-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79349448-A-T

89629765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79349484-G-A

89629765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79349484-G-T

89629766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79349485-G-A

89629766-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79349485-G-C

89629766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79349485-G-T

89629963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79349672-A-G

http://identifiers.org/hco/15/GRCh38#89630085-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#79349774-A-C

89630085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79349774-A-G

http://identifiers.org/hco/15/GRCh38#89630181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#79349845-C-A

89630181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79349845-C-T

89630186-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79349850-G-C

89630186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79349850-G-T

89630491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, splice_region_variant, synonymous_variant, undefined
orthologous variants: 79350134-C-T

89630512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79350155-G-A

89630512-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79350155-G-C

89630512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79350155-G-T

89630560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79350205-T-C

89630560-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79350205-T-G

89630575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79350220-G-A

89630575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79350220-G-T

http://identifiers.org/hco/15/GRCh38#89630595-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#79350240-A-C

http://identifiers.org/hco/15/GRCh38#89630641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#79350280-C-A

89630641-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79350280-C-G

89630641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28704
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79350280-C-T