http://identifiers.org/hco/12/GRCh38#77021422-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#110623076-A-C

77021757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: 3 prime UTR variant
orthologous variants: 110622771-G-T

77021771-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: 3 prime UTR variant
orthologous variants: 110622757-C-G

77022158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: 3 prime UTR variant
orthologous variants: 110622440-T-C

http://identifiers.org/hco/12/GRCh38#77022171-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#110622410-A-C

77022186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: 3 prime UTR variant
orthologous variants: 110622394-A-G

77022206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: 3 prime UTR variant
orthologous variants: 110622369-T-C

77022213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: 3 prime UTR variant
orthologous variants: 110622362-G-T

77022319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: 3 prime UTR variant
orthologous variants: 110622283-G-A

77022419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: 3 prime UTR variant
orthologous variants: 110622166-C-T

http://identifiers.org/hco/12/GRCh38#77022711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#110621910-C-A

77022711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: 3 prime UTR variant
orthologous variants: 110621910-C-T

http://identifiers.org/hco/12/GRCh38#77022849-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#110621814-A-C

77022856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: 3 prime UTR variant
orthologous variants: 110621807-C-T

77022927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: 3 prime UTR variant
orthologous variants: 110621748-A-G

77022977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: 3 prime UTR variant
orthologous variants: 110621686-A-G

77023126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: 3 prime UTR variant
orthologous variants: 110621540-T-C

77023197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: 3 prime UTR variant
orthologous variants: 110621469-T-C

77023404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: 3 prime UTR variant
orthologous variants: 110621271-G-T

77023612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: 3 prime UTR variant
orthologous variants: 110621059-G-T

http://identifiers.org/hco/12/GRCh38#77023641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#110621035-C-A

77023785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: 3 prime UTR variant
orthologous variants: 110620950-G-A

77023785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: 3 prime UTR variant
orthologous variants: 110620950-G-T

http://identifiers.org/hco/12/GRCh38#77023790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#110620945-C-A

77023790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: 3 prime UTR variant
orthologous variants: 110620945-C-T

77023805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: 3 prime UTR variant
orthologous variants: 110620930-A-G

http://identifiers.org/hco/12/GRCh38#77023806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#110620929-C-A

http://identifiers.org/hco/12/GRCh38#77023817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#110620913-C-A

77023817-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: 3 prime UTR variant
orthologous variants: 110620913-C-G

77023817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: 3 prime UTR variant
orthologous variants: 110620913-C-T

77023874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: 3 prime UTR variant
orthologous variants: 110620850-G-T

77023879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: 3 prime UTR variant
orthologous variants: 110620845-T-C

77023908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: 3 prime UTR variant
orthologous variants: 110620814-A-G

77023978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: 3 prime UTR variant
orthologous variants: 110620739-G-A

77024001-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: 3 prime UTR variant
orthologous variants: 110620711-G-C

http://identifiers.org/hco/12/GRCh38#77024037-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#110620675-A-C

77024037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 110620675-A-G

77024105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 110620607-G-T

77024232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron variant
orthologous variants: 110620491-T-C

http://identifiers.org/hco/12/GRCh38#77024252-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#110620475-A-C

http://identifiers.org/hco/12/GRCh38#77024266-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#110620463-C-A

77024266-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron variant
orthologous variants: 110620463-C-G

77024408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron variant
orthologous variants: 110620355-G-A

77024470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron variant
orthologous variants: 110620276-A-G

http://identifiers.org/hco/12/GRCh38#77025436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#110618593-C-A

77025436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron variant
orthologous variants: 110618593-C-T

77025451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron variant
orthologous variants: 110618578-G-A

77025451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron variant
orthologous variants: 110618578-G-T

http://identifiers.org/hco/12/GRCh38#77025453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#110618576-C-A

77025463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron variant
orthologous variants: 110618566-G-A

77025463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron variant
orthologous variants: 110618566-G-T

77025507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron variant
orthologous variants: 110618518-G-T

77025574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, missense_variant
orthologous variants: 110618462-A-G

http://identifiers.org/hco/12/GRCh38#77025592-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#110618444-A-C

77025618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 110618421-G-A

77025634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, missense_variant
orthologous variants: 110618405-C-T

77025642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 110618397-C-T

77025696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 110618343-G-A

77025696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 110618343-G-T

77025948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 110618091-A-G

77026033-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron variant
orthologous variants: 110618012-A-T

77026053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron variant
orthologous variants: 110617992-T-C

http://identifiers.org/hco/12/GRCh38#77026054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#110617991-C-A

77026054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron variant
orthologous variants: 110617991-C-T

http://identifiers.org/hco/12/GRCh38#77027582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#110617186-C-A

77027582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron variant
orthologous variants: 110617186-C-T

77027609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron variant
orthologous variants: 110617159-T-C

77027697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron variant
orthologous variants: 110617020-A-G

http://identifiers.org/hco/12/GRCh38#77027759-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#110616971-A-C

http://identifiers.org/hco/12/GRCh38#77027777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#110616956-C-A

http://identifiers.org/hco/12/GRCh38#77027784-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#110616949-A-C

77027784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron variant
orthologous variants: 110616949-A-G

77027793-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron variant
orthologous variants: 110616940-T-A

77027814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron variant
orthologous variants: 110616920-A-G

77027855-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron variant
orthologous variants: 110616899-G-C

http://identifiers.org/hco/12/GRCh38#77027976-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#110616788-A-C

77028088-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: missense variant
orthologous variants: 110616676-C-G

http://identifiers.org/hco/12/GRCh38#77029715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#110615270-C-A

77029754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron variant
orthologous variants: 110615228-A-G

77029754-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron variant
orthologous variants: 110615228-A-T

77029812-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron variant
orthologous variants: 110615180-T-A

77029812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron variant
orthologous variants: 110615180-T-C

77029812-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron variant
orthologous variants: 110615180-T-G

77029844-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: missense variant
orthologous variants: 110615148-A-T

77029895-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: missense variant
orthologous variants: 110615097-T-A

77029895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: missense variant
orthologous variants: 110615097-T-C

77029895-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: missense variant
orthologous variants: 110615097-T-G

77029958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: missense variant
orthologous variants: 110615031-A-G

77030021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: missense variant
orthologous variants: 110614974-G-A

77030021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: missense variant
orthologous variants: 110614974-G-T

http://identifiers.org/hco/12/GRCh38#77030116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#110614879-C-A

77030116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: synonymous variant
orthologous variants: 110614879-C-T

http://identifiers.org/hco/12/GRCh38#77030138-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#110614857-A-C

http://identifiers.org/hco/12/GRCh38#77030213-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#110614782-A-C

77030213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: missense variant
orthologous variants: 110614782-A-G

77030243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: missense variant
orthologous variants: 110614752-T-C

http://identifiers.org/hco/12/GRCh38#77030330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: missense_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#110614680-C-A

77030368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron variant
orthologous variants: 110614654-T-C

http://identifiers.org/hco/12/GRCh38#77030720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#110614368-C-A

77030963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron variant
orthologous variants: 110614152-A-G

77032252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron variant
orthologous variants: 110612124-G-A

http://identifiers.org/hco/12/GRCh38#77032399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#110611810-C-A

77032551-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron variant
orthologous variants: 110611687-T-A

77032582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron variant
orthologous variants: 110611654-C-T

77032793-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron variant
orthologous variants: 110611489-G-C

77032900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron variant
orthologous variants: 110611394-A-G

http://identifiers.org/hco/12/GRCh38#77032956-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#110611340-A-C

77033018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron variant
orthologous variants: 110611279-G-A

77033018-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron variant
orthologous variants: 110611279-G-C

77033018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron variant
orthologous variants: 110611279-G-T

http://identifiers.org/hco/12/GRCh38#77033030-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#110611267-A-C

77033030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron variant
orthologous variants: 110611267-A-G

77033030-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron variant
orthologous variants: 110611267-A-T

77033216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron variant
orthologous variants: 110611102-T-C

77033266-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron variant
orthologous variants: 110611040-T-A

77033765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron variant
orthologous variants: 110610766-G-T

77033782-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron variant
orthologous variants: 110610749-C-G

77033782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron variant
orthologous variants: 110610749-C-T

77033846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron variant
orthologous variants: 110610697-A-G

77033849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 110610694-G-A

77033946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: missense variant
orthologous variants: 110610597-C-T

http://identifiers.org/hco/12/GRCh38#77033971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#110610572-C-A

77033971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: missense variant
orthologous variants: 110610572-C-T

77034003-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: missense variant
orthologous variants: 110610540-T-A

77034111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110610436-G-T

77034115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110610432-T-C

http://identifiers.org/hco/12/GRCh38#77034151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#110610270-C-A

77034151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110610270-C-T

http://identifiers.org/hco/12/GRCh38#77034159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#110610262-C-A

http://identifiers.org/hco/12/GRCh38#77034165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#110610256-C-A

77034165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110610256-C-T

77034178-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110610190-A-T

77034222-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110610148-T-G

77034226-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110610144-T-A

77034375-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110610000-G-C

77034527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110609854-T-C

http://identifiers.org/hco/12/GRCh38#77034557-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#110609824-A-C

77034557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110609824-A-G

77034558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110609823-A-G

http://identifiers.org/hco/12/GRCh38#77034657-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#110609755-A-C

77034658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110609754-T-C

77034718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110609697-C-T

77034995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110609420-C-T

77035193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110609250-G-A

77042584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110603563-C-T

77042779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110603405-G-A

77042954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110603214-G-T

http://identifiers.org/hco/12/GRCh38#77043028-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#110603149-A-C

77043052-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110603123-C-G

77043052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110603123-C-T

http://identifiers.org/hco/12/GRCh38#77043243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#110602937-C-A

77043243-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110602937-C-G

77043243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110602937-C-T

77043269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110602911-G-A

77043284-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110602896-T-G

77043334-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110602856-T-A

77043334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110602856-T-C

77043334-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110602856-T-G

77043415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110602787-C-T

77043472-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110602734-T-G

77043496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110602714-G-A

77043553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110602635-C-T

http://identifiers.org/hco/12/GRCh38#77043698-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#110602485-A-C

77043868-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110602302-C-G

77043898-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110602279-T-A

77044102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110602153-G-A

77044102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110602153-G-T

http://identifiers.org/hco/12/GRCh38#77044103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#110602152-C-A

77044146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110602126-A-G

77044146-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110602126-A-T

http://identifiers.org/hco/12/GRCh38#77044168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#110602111-C-A

77044168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110602111-C-T

http://identifiers.org/hco/12/GRCh38#77044182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#110602098-C-A

77044182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110602098-C-T

77044283-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110601984-T-A

77044283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110601984-T-C

http://identifiers.org/hco/12/GRCh38#77044453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#110601810-C-A

77044453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110601810-C-T

77044531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110601741-A-G

77044654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 110601616-T-C

77044788-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 110601482-T-G

77044853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110601419-T-C

77044877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110601395-T-C

77044931-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110601342-A-T

77045001-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110601274-A-T

77045007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110601268-C-T

77045038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110601236-T-C

77045135-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110601088-G-C

77045167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110600956-A-G

http://identifiers.org/hco/12/GRCh38#77045528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#110600549-C-A

77045528-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110600549-C-G

77045528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110600549-C-T

77045539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110600530-A-G

77045539-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110600530-A-T

77045638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110600388-T-C

77045822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110600243-T-C

http://identifiers.org/hco/12/GRCh38#77045934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#110600156-C-A

77045950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110600132-G-A

77045950-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110600132-G-C

77045950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110600132-G-T

http://identifiers.org/hco/12/GRCh38#77046016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#110600098-C-A

77046055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110600059-T-C

77046088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110600026-T-C

77046136-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110599978-T-A

77046136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110599978-T-C

77046217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110599897-T-C

77046229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110599885-T-C

http://identifiers.org/hco/12/GRCh38#77046244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#110599870-C-A

77046244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110599870-C-T

77046283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110599831-G-A

77046283-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110599831-G-C

77046283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 110599831-G-T

http://identifiers.org/hco/12/GRCh38#77046358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#110599756-C-A

77046358-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110599756-C-G

77046358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110599756-C-T

http://identifiers.org/hco/12/GRCh38#77046370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#110599744-C-A

77046370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110599744-C-T

77046393-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110599721-A-T

http://identifiers.org/hco/12/GRCh38#77046409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#110599715-C-A

77046598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110599521-A-G

77047123-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110598932-A-T

77047135-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110598920-G-C

77047405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110598688-T-C

77047415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110598678-C-T

77047481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110598612-T-C

77047604-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110598479-T-A

77047651-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110598430-C-G

77047802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110598291-G-A

77047837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110598266-G-A

77047837-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110598266-G-C

77047846-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110598257-G-C

http://identifiers.org/hco/12/GRCh38#77047906-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#110598197-A-C

77047906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110598197-A-G

77047937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110598166-C-T

77047990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110598111-T-C

77048123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110597989-T-C

77048364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110597749-T-C

77048509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110597586-T-C

77048544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110597555-G-T

77048689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110597410-C-T

77048758-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110597348-C-G

77048759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110597347-T-C

77048838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110597300-G-A

77048838-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110597300-G-C

77048849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110597288-C-T

77048885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110597250-G-A

77048914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110597222-T-C

77048931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110597189-G-A

77048992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110597130-T-C

77049706-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110596878-T-G

http://identifiers.org/hco/12/GRCh38#77049910-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#110596697-A-C

77050111-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110596487-C-G

77050369-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110596094-T-G

77050429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110596008-T-C

77050436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110596001-A-G

77050483-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110595955-G-C

77050483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110595955-G-T

http://identifiers.org/hco/12/GRCh38#77050501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#110595923-C-A

77050501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110595923-C-T

http://identifiers.org/hco/12/GRCh38#77050505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#110595919-C-A

77050505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110595919-C-T

77050513-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110595911-C-G

77050530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110595894-C-T

77050635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110595786-C-T

http://identifiers.org/hco/12/GRCh38#77050734-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#110595687-A-C

77050734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110595687-A-G

77050816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110595609-A-G

http://identifiers.org/hco/12/GRCh38#77050851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#110595580-C-A

77050851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110595580-C-T

77050884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110595549-A-G

77051029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110595407-C-T

77051030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110595406-G-A

77051793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110594691-C-T

77051823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110594661-G-A

77052267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110594292-A-G

http://identifiers.org/hco/12/GRCh38#77052268-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#110594291-A-C

http://identifiers.org/hco/12/GRCh38#77052531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#110594036-C-A

77052887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110593699-A-G

77052906-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110593680-T-G

77052955-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110593630-C-G

77053730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110592774-A-G

77053785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110592717-T-C

77054946-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110592366-A-T

77055170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110592155-T-C

77055197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110592128-G-A

77055727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110590330-A-G

77055742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110590315-G-T

http://identifiers.org/hco/12/GRCh38#77055743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#110590314-C-A

77055743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110590314-C-T

http://identifiers.org/hco/12/GRCh38#77055746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#110590310-C-A

77055766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110590289-G-A

77055766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110590289-G-T

77055785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110590285-T-C

77055788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110590282-G-T

77055798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110590272-T-C

http://identifiers.org/hco/12/GRCh38#77055832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#110590237-C-A

77055832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110590237-C-T

77055858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 110590215-T-C

77055898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110590175-C-T

77055982-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110590091-C-G

77055985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110590088-G-T

77056069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110590001-A-G

77056078-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110589992-T-G

http://identifiers.org/hco/12/GRCh38#77056111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#110589959-C-A

77056111-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110589959-C-G

77056111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110589959-C-T

77056190-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110589873-T-A

77056223-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110589854-A-T

http://identifiers.org/hco/12/GRCh38#77056236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#110589841-C-A

77056236-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110589841-C-G

77056236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110589841-C-T

77056317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110589759-T-C

77056432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110589644-A-G

77056432-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110589644-A-T

77056447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110589634-A-G

http://identifiers.org/hco/12/GRCh38#77056514-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#110589567-A-C

77056552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110589540-C-T

77056616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110589489-C-T

77057565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110589165-T-C

77057571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110589159-T-C

77057901-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110588879-T-G

77058163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110588302-G-A

77058398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110587731-G-A

77058779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110587381-A-G

http://identifiers.org/hco/12/GRCh38#77058852-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#110587304-A-C

77058854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110587302-G-A

77059069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110587121-A-G

77060003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110585856-C-T

77060813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110585067-C-T

77061088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110584813-A-G

77061557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110584359-A-G

http://identifiers.org/hco/12/GRCh38#77061654-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#110584266-A-C

77061719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110584204-C-T

77061774-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110584153-T-A

77061864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110584080-T-C

77061898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110584050-T-C

77062071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110583921-C-T

77062188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110583815-A-G

77062269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110583736-C-T

77062317-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110583688-G-C

77062367-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110583638-A-T

77062509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110583509-C-T

77062845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110583211-T-C

77063806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110582953-C-T

77064509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110582319-C-T

http://identifiers.org/hco/12/GRCh38#77064567-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#110582259-A-C

77064567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 110582259-A-G

77064755-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110582085-T-A

77064990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110581855-A-G

77065162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110581670-T-C

77065177-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110581668-G-C

77065362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 110581521-G-A

77065430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 110581459-G-A

77065430-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 110581459-G-C

77065430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23820
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 110581459-G-T