122271417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: 5 prime UTR variant
orthologous variants: 130376006-G-A

122271417-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: 5 prime UTR variant
orthologous variants: 130376006-G-C

122271453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: 5 prime UTR variant
orthologous variants: 130376042-T-C

122271546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130376130-A-G

122271645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130376195-G-A

122274430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 130378153-T-C

122274553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 130378262-T-C

122274564-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 130378273-G-C

122274818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 130378521-T-C

122274889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 130378653-C-T

122274964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 130378729-G-T

122275147-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130379669-T-G

http://identifiers.org/hco/10/GRCh38#122275149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130379671-C-A

122275149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130379671-C-T

http://identifiers.org/hco/10/GRCh38#122275192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130379713-C-A

122275192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130379713-C-T

122275278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130379797-T-C

122275309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130379821-A-G

122275396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130379890-T-C

122275448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130379943-T-C

122276166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130380737-T-C

122276210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130380781-G-T

122276213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130380784-A-G

122276288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130380855-T-C

122276298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130380865-G-A

122276298-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130380865-G-C

122276305-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130380872-T-A

122276309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130380876-G-A

http://identifiers.org/hco/10/GRCh38#122276522-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130381062-A-C

122276886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130381382-G-A

122276901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130381397-G-A

122276907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, missense_variant
orthologous variants: 130381403-A-G

122276910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130381406-C-T

122276955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130381451-G-T

122276956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130381452-G-A

122276956-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130381452-G-C

122277015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130381507-C-T

122277021-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130381513-T-G

122277298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130381739-G-A

122277308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130381749-A-G

http://identifiers.org/hco/10/GRCh38#122277877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130381876-C-A

122277935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130381931-G-A

122277935-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130381931-G-C

122277968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130381964-G-T

122280000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130382818-C-T

122280210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130382942-A-G

122280218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130382950-T-C

122280303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130383027-G-A

122280357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130383080-C-T

122280386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130383110-C-T

122281752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130383690-A-G

122281916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130383840-C-T

122281924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130383848-C-T

122282145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130384028-G-T

122282302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130384172-G-A

122282435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130384302-G-A

http://identifiers.org/hco/10/GRCh38#122282478-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130384344-A-C

122282478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130384344-A-G

122282536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130384402-A-G

122282669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130384552-G-T

122282781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130384662-C-T

122282814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130384692-G-T

122283282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130385097-C-T

122283490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130385362-G-T

122283807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130385947-G-A

http://identifiers.org/hco/10/GRCh38#122283825-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130385965-A-C

http://identifiers.org/hco/10/GRCh38#122283869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130386009-C-A

122283869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130386009-C-T

http://identifiers.org/hco/10/GRCh38#122283881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130386021-C-A

122284017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130386152-G-A

122284036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130386171-G-A

122284046-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130386181-T-A

http://identifiers.org/hco/10/GRCh38#122284654-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130386597-A-C

122284743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130386664-A-G

122284894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130386817-G-A

122284911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130386833-T-C

122284967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130386876-T-C

122284985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130386897-C-T

http://identifiers.org/hco/10/GRCh38#122285201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130387101-C-A

122285855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130387412-C-T

http://identifiers.org/hco/10/GRCh38#122285972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130387497-C-A

122285972-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130387497-C-G

122285972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130387497-C-T

122285992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130387517-G-A

122285992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130387517-G-T

122286001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130387526-G-A

122286001-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130387526-G-T

http://identifiers.org/hco/10/GRCh38#122286002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130387527-C-A

122286002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130387527-C-T

122286044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130387557-G-T

122286202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130387769-G-A

122286202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130387769-G-T

http://identifiers.org/hco/10/GRCh38#122286210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130387777-C-A

122286210-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, missense_variant
orthologous variants: 130387777-C-G

122286210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, missense_variant
orthologous variants: 130387777-C-T

122286274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130387840-T-C

122286281-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130387847-C-G

122286281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130387847-C-T

122286284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130387850-G-T

http://identifiers.org/hco/10/GRCh38#122286300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130387866-C-A

122286300-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130387866-C-G

122286300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130387866-C-T

122286308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130387876-G-A

122286308-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130387876-G-C

122286308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130387876-G-T

122287006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130388023-G-A

122287016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130388033-G-A

122287046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130388060-C-T

122287103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130388105-G-A

122287136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130388132-G-A

122287168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130388163-G-T

http://identifiers.org/hco/10/GRCh38#122287286-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130388278-C-A

122287297-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130388289-T-G

122287302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130388293-G-T

122287364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130388355-G-A

122287438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130388421-C-T

122287559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130388516-A-G

http://identifiers.org/hco/10/GRCh38#122287644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130388591-C-A

122287685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130388632-T-C

http://identifiers.org/hco/10/GRCh38#122287717-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130388683-A-C

122287825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130388791-G-A

122287944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130388897-C-T

122288126-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130389034-C-G

122288519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130389434-G-A

122288519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130389434-G-T

122288712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130389616-T-C

http://identifiers.org/hco/10/GRCh38#122288763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130389661-C-A

122288806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130389708-G-A

122288937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130389839-T-C

122289894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130390475-C-T

122289919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 130390500-T-C

122289919-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 130390500-T-G

122289928-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 130390509-C-G

122289942-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 130390523-C-G

122290002-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130390584-T-G

122290144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130390924-A-G

122290163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130390943-G-A

122290288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130391113-G-T

122290344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130391177-A-G

122290368-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130391201-A-T

122290393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130391230-C-T

122290536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130391403-C-T

122290587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130391487-C-T

122290619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130391518-T-C

122290682-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130391581-C-G

122290827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130391703-C-T

122290997-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130391874-G-C

122290997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130391874-G-T

http://identifiers.org/hco/10/GRCh38#122290998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130391875-C-A

122291010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130391886-G-A

122291010-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130391886-G-T

122291056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130391927-G-A

http://identifiers.org/hco/10/GRCh38#122291059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130391930-C-A

122291059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130391930-C-T

122291249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130392112-G-A

122291249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130392112-G-T

122291257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130392120-T-C

http://identifiers.org/hco/10/GRCh38#122291334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130392165-C-A

122291373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130392208-A-G

http://identifiers.org/hco/10/GRCh38#122291384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130392217-C-A

122291446-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 130392300-G-T

122291468-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 130392322-T-G

122291470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 130392324-C-T

122291474-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 130392328-T-G

http://identifiers.org/hco/10/GRCh38#122291488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130392342-C-A

122291488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 130392342-C-T

122291514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 130392360-T-C

122293390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, undefined
orthologous variants: 130392928-G-T

122293552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130393117-A-G

122293659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130393224-C-T

122293676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130393241-A-G

122293820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130393365-C-T

http://identifiers.org/hco/10/GRCh38#122293982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130393519-C-A

122293982-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130393519-C-G

122293982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130393519-C-T

122293996-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130393533-T-A

122294031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130393568-A-G

http://identifiers.org/hco/10/GRCh38#122294032-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130393569-A-C

122294032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130393569-A-G

http://identifiers.org/hco/10/GRCh38#122294279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130393706-C-A

122294279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130393706-C-T

122294280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130393707-A-G

http://identifiers.org/hco/10/GRCh38#122294323-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130393749-A-C

122294404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130393824-G-A

122294433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130393855-A-G

122294509-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130393931-C-G

122294509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130393931-C-T

122295811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130395044-T-C

122295864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130395098-C-T

122295981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130395196-A-G

122296178-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130395387-T-G

122296364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130395528-C-T

122296543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130395894-G-A

http://identifiers.org/hco/10/GRCh38#122296590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130395932-C-A

http://identifiers.org/hco/10/GRCh38#122296659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130396001-C-A

122296659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130396001-C-T

122296893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130396088-G-A

122296935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130396130-G-A

122296965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130396158-G-A

122297018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130396211-A-G

122297122-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130396335-T-G

122297275-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130396560-T-G

122297286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130396571-G-A

122297348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130396632-T-C

http://identifiers.org/hco/10/GRCh38#122297352-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130396636-A-C

122297352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130396636-A-G

122297537-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130396795-T-A

122297652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130396903-T-C

http://identifiers.org/hco/10/GRCh38#122297664-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130396918-A-C

http://identifiers.org/hco/10/GRCh38#122297680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130396935-C-A

http://identifiers.org/hco/10/GRCh38#122297712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130396986-C-A

122297712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130396986-C-T

http://identifiers.org/hco/10/GRCh38#122297745-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130397016-A-C

http://identifiers.org/hco/10/GRCh38#122297756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130397027-C-A

122297756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130397027-C-T

122297795-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130397066-C-G

122297885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130397160-G-A

122297886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130397161-G-A

122297918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130397191-G-T

122298160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130397444-G-A

122298160-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130397444-G-T

122298188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130397469-T-C

122298279-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130397568-C-G

122298329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130397647-G-T

122298330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130397648-G-T

122298351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130397691-A-G

122298407-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130397773-G-C

http://identifiers.org/hco/10/GRCh38#122298652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130398263-C-A

122298657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130398268-G-A

122298657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130398268-G-T

122298681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130398302-G-A

122298692-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130398313-T-G

122298711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130398345-A-G

122298853-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, undefined
orthologous variants: 130398549-G-C

122298853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, undefined
orthologous variants: 130398549-G-T

122299099-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130398797-A-T

122299129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 130398827-C-T

122299188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, undefined
orthologous variants: 130398879-G-A

122299188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, undefined
orthologous variants: 130398879-G-T

122299209-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130398898-T-A

122299209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130398898-T-C

122299209-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130398898-T-G

122299217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130398910-T-C

http://identifiers.org/hco/10/GRCh38#122299235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130398929-C-A

122299235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130398929-C-T

122299327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130399044-G-A

122299432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130399148-A-G

122299619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130399325-A-G

122299777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130399452-C-T

122299848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130399531-A-G

122299932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130399583-C-T

122300027-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130399669-G-C

122300067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130399695-A-G

122300083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130399711-G-A

http://identifiers.org/hco/10/GRCh38#122301248-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130401441-A-C

122301261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130401456-G-A

122302160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130402528-C-T

122302184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130402553-C-T

122302484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130402845-C-T

122303481-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130405326-A-T

http://identifiers.org/hco/10/GRCh38#122303565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130405404-C-A

122303565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130405404-C-T

122303613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130405452-A-G

122303677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130405521-T-C

122303677-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130405521-T-G

122303685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130405529-G-T

http://identifiers.org/hco/10/GRCh38#122303713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130405558-C-A

122303713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130405558-C-T

122304331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130405914-G-T

122304490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130406046-G-T

122304500-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130406056-T-A

122304591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130406133-G-T

122304642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130406146-C-T

http://identifiers.org/hco/10/GRCh38#122304765-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130406170-A-C

122304765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130406170-A-G

122304766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130406171-G-A

http://identifiers.org/hco/10/GRCh38#122304839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130406238-C-A

122304938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130406290-G-A

122304938-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130406290-G-C

122306382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130406811-T-C

122306464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130406901-C-T

122306477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130406913-A-G

122306573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130406959-C-T

122306615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130406994-C-T

122306634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130407006-T-C

122306688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130407093-C-T

122306955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130407336-G-A

122307059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130407425-T-C

122307059-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130407425-T-G

122307077-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130407444-G-C

122307077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130407444-G-T

122307177-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130407539-T-A

122307313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130407675-T-C

http://identifiers.org/hco/10/GRCh38#122307318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130407680-C-A

122307318-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130407680-C-G

122307318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130407680-C-T

122307330-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130407692-T-G

122307339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130407701-A-G

122308243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130409729-G-A

122324679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130412086-G-T

122324723-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130412128-C-G

122324763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130412169-C-T

122324771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130412177-C-T

122324800-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130412211-C-G

122325087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130412537-A-G

122325239-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130412641-A-T

122325418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130412837-C-T

122325463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130412882-A-G

122326036-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130413092-T-A

122326267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130413322-C-T

122326370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130413413-G-A

122326370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130413413-G-T

122326443-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130413479-T-G

122326498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130414205-G-A

122326599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130414309-T-C

122326686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130414417-A-G

122326690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130414421-G-T

122326885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130414580-G-A

122327187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130414946-C-T

122327281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130415025-A-G

122327335-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130415078-A-T

122327357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130415097-G-A

122327357-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130415097-G-T

http://identifiers.org/hco/10/GRCh38#122327456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130415187-C-A

122327456-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130415187-C-G

122327572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130415297-G-A

122327572-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130415297-G-C

122327637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130415358-G-T

122327938-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130415628-C-G

122328630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130416512-T-C

122328630-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130416512-T-G

122328708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130416784-G-A

122328722-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, undefined
orthologous variants: 130416798-C-G

122328827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130416890-C-T

122329098-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130417137-T-A

122329107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130417146-C-T

122329334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130417334-A-G

122329427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130417401-T-C

122329558-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: missense variant
orthologous variants: 130417524-C-G

122329558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: synonymous variant
orthologous variants: 130417524-C-T

http://identifiers.org/hco/10/GRCh38#122329624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130417587-C-A

122329624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130417587-C-T

122329643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130417620-G-A

122329643-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130417620-G-C

122329643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130417620-G-T

http://identifiers.org/hco/10/GRCh38#122329682-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130417654-A-C

http://identifiers.org/hco/10/GRCh38#122329955-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130418538-A-C

122330108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130418693-A-G

122330266-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130418851-T-A

122331266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 130420838-G-A

122331266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 130420838-G-T

122331397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130420966-G-A

122331711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130421506-A-G

122331749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, undefined
orthologous variants: 130421544-C-T

122331855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, undefined
orthologous variants: 130421655-A-G

http://identifiers.org/hco/10/GRCh38#122332014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#130421792-C-A

122332014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 130421792-C-T

122332125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 130421897-T-C

122332125-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 130421897-T-G

122332160-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 130421929-G-T

122332171-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 130421950-A-T

http://identifiers.org/hco/10/GRCh38#122332268-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130422055-C-A

122332268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130422055-C-T

122332346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130422087-G-A

122332346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130422087-G-T

http://identifiers.org/hco/10/GRCh38#122332392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130422131-C-A

122332392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130422131-C-T

122332421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130422153-G-T

122332474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 130422206-T-C

122332592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130422332-A-G

122332592-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130422332-A-T

http://identifiers.org/hco/10/GRCh38#122332984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130422673-C-A

http://identifiers.org/hco/10/GRCh38#122333015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130422706-C-A

122333036-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130422723-T-A

http://identifiers.org/hco/10/GRCh38#122333058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130422742-C-A

122333100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130422778-T-C

122333210-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130422858-C-G

http://identifiers.org/hco/10/GRCh38#122334853-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130423133-A-C

122334855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130423135-T-C

122335121-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130423389-T-A

122335494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130423754-G-A

122335494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130423754-G-T

122335993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130424419-T-C

122336042-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130424472-C-G

122336096-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130424522-G-C

122336331-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130424726-T-A

http://identifiers.org/hco/10/GRCh38#122336353-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130424746-A-C

122336353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130424746-A-G

122336357-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130424750-G-T

http://identifiers.org/hco/10/GRCh38#122336465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130424855-C-A

122336465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130424855-C-T

122336478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130424868-A-G

http://identifiers.org/hco/10/GRCh38#122336554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130424944-C-A

122336554-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 130424944-C-G

122336727-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130425131-T-G

http://identifiers.org/hco/10/GRCh38#122336769-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130425175-A-C

122336769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130425175-A-G

122336798-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130425192-T-A

122336798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130425192-T-C

122336798-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130425192-T-G

122336806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130425200-A-G

http://identifiers.org/hco/10/GRCh38#122336825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130425219-C-A

122336825-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130425219-C-G

122336825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130425219-C-T

122336827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130425221-G-A

122336827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130425221-G-T

122336832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130425226-A-G

122337050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130425386-C-T

122337213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130425626-C-T

122337287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130425701-T-C

122337342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130425747-G-A

122337417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: 130425815-A-G

http://identifiers.org/hco/10/GRCh38#122337988-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130426013-C-A

122338052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: synonymous variant
orthologous variants: 130426074-T-C

122338086-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: 3 prime UTR variant
orthologous variants: 130426108-C-G

122338086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: 3 prime UTR variant
orthologous variants: 130426108-C-T

122338093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26340
most severe consequence: 3 prime UTR variant
orthologous variants: 130426115-C-T