99098303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 67415439-C-T

99098308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 67415435-A-G

99098311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 67415432-G-A

99098311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 67415432-G-T

99098348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 67415404-G-A

http://identifiers.org/hco/15/GRCh38#99098393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#67415377-C-A

99098393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 67415377-C-T

99098397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 67415373-T-C

99098397-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 67415373-T-G

http://identifiers.org/hco/15/GRCh38#99098461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#67415327-C-A

99098473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 67415315-T-C

99098515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 67415272-C-T

99098554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 67415223-A-G

99098554-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 67415223-A-T

99098596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 67415181-C-T

99098858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: 67415105-T-C

99098888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: 67415072-C-T

99098960-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: 67415048-G-C

99098980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: 67415028-C-T

http://identifiers.org/hco/15/GRCh38#99098995-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#67415013-A-C

http://identifiers.org/hco/15/GRCh38#99099160-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#67414904-C-A

http://identifiers.org/hco/15/GRCh38#99099173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#67414891-C-A

http://identifiers.org/hco/15/GRCh38#99099186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#67414878-C-A

99099232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: 67414831-G-A

99099321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: 67414695-T-C

99099411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: 67414630-G-A

99099411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: 67414630-G-T

http://identifiers.org/hco/15/GRCh38#99099461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#67414584-C-A

99099563-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: 67414478-G-C

http://identifiers.org/hco/15/GRCh38#99099746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#67414369-C-A

99099746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: 67414369-C-T

99099752-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: 67414363-G-C

99099778-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: 67414337-G-C

99099790-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: 67414327-C-G

99100230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: 67413878-A-G

99100280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: 67413810-A-G

99101218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: 67412404-C-T

99101630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: 67412089-G-A

99102075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: 67411780-T-C

99102147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: 67411707-T-C

99102186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: 67411669-G-A

99102373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: 67411524-C-T

99102491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: 67411406-T-C

99102516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: 67411377-G-A

99102772-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: 67411121-A-T

99102825-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: 67411071-C-G

99102837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: 67411059-C-T

99103034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: 67410893-C-T

99103058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: 67410869-G-A

99103058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: 67410869-G-T

http://identifiers.org/hco/15/GRCh38#99103103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#67410839-C-A

99103586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: 67410717-C-T

99103664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: 67410642-G-A

http://identifiers.org/hco/15/GRCh38#99103763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#67410520-C-A

99103779-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: 67410504-G-C

99103890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: 67410391-T-C

99103913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: 67410368-G-A

99103918-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: 67410363-C-G

http://identifiers.org/hco/15/GRCh38#99104021-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#67410258-A-C

99104754-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: 67409833-G-C

99104834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: 67409758-C-T

99104993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: 67409563-G-T

99105001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: 67409555-G-A

99105001-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: 67409555-G-C

99105001-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: 67409555-G-T

http://identifiers.org/hco/15/GRCh38#99105029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#67409538-C-A

99105029-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: 67409538-C-G

99105029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: 67409538-C-T

http://identifiers.org/hco/15/GRCh38#99105041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#67409527-C-A

99105041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: 67409527-C-T

99105055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: 67409513-G-A

99105055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: 67409513-G-T

http://identifiers.org/hco/15/GRCh38#99105057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#67409511-C-A

99105057-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: 67409511-C-G

99105057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: 67409511-C-T

99105104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 67409464-G-A

99105104-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 67409464-G-C

http://identifiers.org/hco/15/GRCh38#99105105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#67409463-C-A

99105105-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 67409463-C-G

99105105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 67409463-C-T

99105130-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 67409438-G-C

99105130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 67409438-G-T

99105141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 67409433-G-A

99105141-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 67409433-G-C

99105141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 67409433-G-T

http://identifiers.org/hco/15/GRCh38#99105166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#67409408-C-A

99105166-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 67409408-C-G

99105166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 67409408-C-T

http://identifiers.org/hco/15/GRCh38#99105193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#67409381-C-A

99105193-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 67409381-C-G

99105193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 67409381-C-T

99105254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 67409320-A-G

http://identifiers.org/hco/15/GRCh38#99105374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#67409200-C-A

99105374-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 67409200-C-G

99105374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 67409200-C-T

99105453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 67409121-G-A

99105453-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 67409121-G-C

99105453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 67409121-G-T

http://identifiers.org/hco/15/GRCh38#99105482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#67409092-C-A

99105482-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 67409092-C-G

99105482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 67409092-C-T

http://identifiers.org/hco/15/GRCh38#99105491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#67409083-C-A

99105491-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 67409083-C-G

99105491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 67409083-C-T

99105503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 67409071-G-A

99105503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, stop_gained, undefined
orthologous variants: 67409071-G-T

99105581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 67408993-G-A

99105581-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 67408993-G-C

99105581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 67408993-G-T

99105627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 67408947-G-A

99105627-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 67408947-G-C

99105627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 67408947-G-T

99105644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 67408930-G-A

99105644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, stop_gained, undefined
orthologous variants: 67408930-G-T

99105776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 67408798-G-A

99105776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, stop_gained, undefined
orthologous variants: 67408798-G-T

99105782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 67408792-T-C

http://identifiers.org/hco/15/GRCh38#99105839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#67408735-C-A

99105839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 67408735-C-T

99105905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 67408669-G-A

99105905-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 67408669-G-C

99105905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 67408669-G-T

http://identifiers.org/hco/15/GRCh38#99105914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#67408660-C-A

99105914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 67408660-C-T

99105920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 67408654-G-A

99105920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 67408654-G-T

http://identifiers.org/hco/15/GRCh38#99105985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, stop_gained, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#67408589-C-A

99105985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 67408589-C-T

http://identifiers.org/hco/15/GRCh38#99106058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#67408515-C-A

99106058-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: 67408515-C-G

99106058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: 67408515-C-T

http://identifiers.org/hco/15/GRCh38#99106069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#67408508-C-A

99106069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: 67408508-C-T

99106074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: 67408503-G-A

99106080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: 67408497-G-A

http://identifiers.org/hco/15/GRCh38#99106121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#67408413-C-A

99106121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: 67408413-C-T

99106123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: 67408411-G-A

99106123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: 67408411-G-T

99106578-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: 67407849-C-G

99106702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: 67407729-C-T

99106847-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: 67407573-A-T

99106884-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: 67407536-T-G

99106994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: 67407440-A-G

99107710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: 67407188-A-G

99108717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67406571-C-T

99108750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67406539-A-G

99108787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67406506-G-A

99108798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67406495-T-C

99108862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67406461-A-G

99108988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67406343-G-A

99108992-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67406339-T-A

99108992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67406339-T-C

99109536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67406083-C-T

99109687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67405912-T-C

99109718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67405883-A-G

99109776-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: 67405792-G-C

99109953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67405457-T-C

99109954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67405456-G-A

99110181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67405230-A-G

99110192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67405219-G-A

99110500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67404898-G-A

99110500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67404898-G-T

99110672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67404747-A-G

99110697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67404722-T-C

99110882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67404546-C-T

99111506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67403770-G-A

99111566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67403708-T-C

99111568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67403706-G-A

99111850-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67403010-T-G

99112451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67402937-C-T

http://identifiers.org/hco/15/GRCh38#99113056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#67402152-C-A

99113056-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67402152-C-G

99113275-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67401936-T-G

99113624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 67401641-A-G

99113817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67401509-G-A

99114891-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67401007-G-C

99114892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67401006-T-C

99115041-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67400885-C-G

99115118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67400810-G-A

99115180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67400748-G-A

99115285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67400628-G-A

99115285-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67400628-G-C

99115373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67400547-T-C

99115972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67400331-C-T

99117204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67399911-T-C

99117235-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67399889-C-G

99117351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67399813-G-A

99117431-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67399741-A-T

99117462-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67399709-C-G

99117611-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67399568-C-G

99117623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67399556-C-T

99117624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67399550-T-C

99117650-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67399519-C-G

99117662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67399507-G-A

99117913-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67399251-A-T

99117986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67399180-C-T

99118372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67398741-G-A

99118561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67398471-C-T

99118673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67398359-G-T

99118841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67398209-C-T

99118893-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67398163-C-G

99118893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67398163-C-T

99119203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67397504-G-A

99119403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67397302-G-T

99119406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67397299-C-T

99119433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67397273-G-A

99119583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67397123-G-A

99119670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67397058-C-T

99120060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67396677-A-G

99120375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67396447-A-G

http://identifiers.org/hco/15/GRCh38#99120498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#67396342-C-A

99120556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67396255-G-A

99120556-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67396255-G-C

99120776-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67396021-A-T

http://identifiers.org/hco/15/GRCh38#99120921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#67395904-C-A

99120985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67395863-G-A

99120985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67395863-G-T

99121229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67395626-G-A

99121434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67395425-G-A

99121484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67395369-C-T

99122264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67393137-G-A

99122607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67392802-A-G

99123202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67392425-C-T

99123225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67392402-C-T

99123255-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67392346-T-A

99123575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67392089-G-A

99123649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67392023-C-T

99123848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67391824-G-A

99124076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67391616-G-A

http://identifiers.org/hco/15/GRCh38#99124232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#67391462-C-A

99124232-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67391462-C-G

99124247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67391443-T-C

99124314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67391391-C-T

99124433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67391244-C-T

99124735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67390972-G-A

99124828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67390924-G-A

99125058-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67390759-G-C

http://identifiers.org/hco/15/GRCh38#99125108-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#67390693-C-A

99125378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67390400-G-T

99125442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67390335-C-T

99125449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67390328-C-T

99125505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67390278-C-T

99125665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67390133-C-T

99125728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67390071-C-T

99126369-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67389292-T-A

99126525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67389089-C-T

99126703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67388941-T-C

99126703-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67388941-T-G

99127035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67388561-G-A

99127083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67388529-A-G

99127217-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67388397-T-A

99127361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67388289-G-A

99127415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67388230-G-A

99127554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67388118-T-C

99127603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67388083-G-A

99127842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67387994-A-G

99127989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67387916-G-T

99128056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67387905-G-T

99128683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67387323-T-C

99128691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67387315-T-C

99128745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron variant
orthologous variants: 67387262-A-G

99129076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: 67386939-T-C

http://identifiers.org/hco/15/GRCh38#99129124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#67386888-C-A

99129124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: 67386888-C-T

http://identifiers.org/hco/15/GRCh38#99129205-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#67386807-A-C

http://identifiers.org/hco/15/GRCh38#99129316-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#67386702-A-C

99129563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 67386456-G-A

99129563-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 67386456-G-C

99129563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 67386456-G-T

http://identifiers.org/hco/15/GRCh38#99129585-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#67386434-A-C

99129623-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 67386393-T-A

99129666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 67386350-A-G

99129673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 67386343-C-T

http://identifiers.org/hco/15/GRCh38#99129682-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#67386334-A-C

99129682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 67386334-A-G

99129691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 67386325-C-T

99129695-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 67386321-C-G

99129733-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 67386283-C-G

99129733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 67386283-C-T

99129737-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 67386279-T-A

99129744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 67386272-G-A

99129746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 67386270-T-C

99129757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 67386259-C-T

99129822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 67386194-C-T

99130112-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 67385904-C-G

99130112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 67385904-C-T

99130154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 67385862-G-A

99130154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 67385862-G-T

99130208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 67385805-A-G

99130335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 67385678-T-C

99130337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 67385676-T-C

http://identifiers.org/hco/15/GRCh38#99130350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#67385663-C-A

99130581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 67385432-G-A

99130596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 67385417-G-A

99130596-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 67385417-G-C

99130765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 67385251-A-G

99130776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 67385243-A-G

99130861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 67385158-C-T

99130881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 67385138-G-A

99131045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 67384971-G-A

99131045-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 67384971-G-C

99131046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 67384970-C-T

99131061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 67384955-G-A

99131061-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 67384955-G-C

99131061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 67384955-G-T

99131062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 67384954-A-G

99131062-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 67384954-A-T

99131070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 67384946-T-C

99131108-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 67384911-T-G

99131154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 67384865-G-A

99131289-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 67384730-G-C

99131293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 67384726-G-A

99131300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 67384719-G-A

99131410-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 67384609-A-T

99131981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 67384044-A-G

99131999-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, missense_variant
orthologous variants: 67384026-T-A

99132206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 67383819-A-G

99132227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 67383798-G-A

99132227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, missense_variant
orthologous variants: 67383798-G-T

http://identifiers.org/hco/15/GRCh38#99132426-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#67383617-C-A

99132562-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, missense_variant
orthologous variants: 67383487-T-G

99132599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 67383450-C-T

99132615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, missense_variant
orthologous variants: 67383434-A-G

99132655-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, stop_gained
orthologous variants: 67383394-C-G

99132655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, missense_variant
orthologous variants: 67383394-C-T

99132659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 67383390-G-A

99132757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: intron_variant, missense_variant, synonymous_variant
orthologous variants: 67383292-T-C

99132984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 67383053-A-G

99133046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 3_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 67382991-G-A

99133046-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 3_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 67382991-G-C

99133047-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 67382990-C-G

99133047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 67382990-C-T

99133070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67382961-A-G

http://identifiers.org/hco/15/GRCh38#99133080-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#67382950-A-C

http://identifiers.org/hco/15/GRCh38#99133137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#67382884-C-A

99133137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67382884-C-T

99133187-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67382836-C-G

99133187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67382836-C-T

99133194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67382829-T-C

99133202-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67382821-T-A

99133211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67382812-A-G

http://identifiers.org/hco/15/GRCh38#99133318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#67382709-C-A

99133318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67382709-C-T

99133325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67382702-G-T

99133339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67382689-A-G

99133339-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67382689-A-T

99133489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67382531-G-A

99133489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67382531-G-T

99133531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67382485-A-G

http://identifiers.org/hco/15/GRCh38#99133826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#67382159-C-A

99133849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67382132-G-A

99133849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67382132-G-T

99134017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67381908-G-T

99134036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67381894-G-A

99134036-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67381894-G-C

99134036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67381894-G-T

99134112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67381812-A-G

99134122-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67381803-C-G

http://identifiers.org/hco/15/GRCh38#99134210-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#67381733-A-C

http://identifiers.org/hco/15/GRCh38#99134252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#67381690-C-A

99134252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67381690-C-T

99134267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67381675-A-G

99134305-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67381639-T-G

99134339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67381605-G-T

http://identifiers.org/hco/15/GRCh38#99134374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#67381574-C-A

99134420-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67381529-T-G

99134634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67381343-T-C

99134640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67381337-T-C

99134664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67381324-A-G

99134694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67381304-G-A

99134725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67381272-T-C

99134757-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67381240-C-G

99134817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67381183-T-C

99134866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67381140-G-A

99134866-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67381140-G-C

99134866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67381140-G-T

99134874-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67381132-G-C

99134932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67381076-G-A

99134982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 67381038-T-C

99135096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67380909-A-G

99135307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67380688-G-A

99135365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67380634-G-T

99135379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67380620-G-A

99135379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 67380620-G-T

http://identifiers.org/hco/15/GRCh38#99136503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 3_prime_UTR_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#67379212-C-A

99136654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 67379054-C-T

99136813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24466
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 67378867-G-A