http://identifiers.org/hco/18/GRCh38#58481257-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65398610-A-C

58481288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: 3 prime UTR variant
orthologous variants: 65398641-C-T

http://identifiers.org/hco/18/GRCh38#58481318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65398675-C-A

58481318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: 3 prime UTR variant
orthologous variants: 65398675-C-T

58481349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: 3 prime UTR variant
orthologous variants: 65398706-G-A

58481351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: 3 prime UTR variant
orthologous variants: 65398708-A-G

58481352-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: 3 prime UTR variant
orthologous variants: 65398709-T-A

58481491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: 3 prime UTR variant
orthologous variants: 65398814-A-G

58481491-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: 3 prime UTR variant
orthologous variants: 65398814-A-T

58481514-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: 3 prime UTR variant
orthologous variants: 65398840-T-A

58481514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: 3 prime UTR variant
orthologous variants: 65398840-T-C

58481556-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: 3 prime UTR variant
orthologous variants: 65398894-T-A

58481556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: 3 prime UTR variant
orthologous variants: 65398894-T-C

58481556-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: 3 prime UTR variant
orthologous variants: 65398894-T-G

58481603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: 3 prime UTR variant
orthologous variants: 65398941-G-A

58481603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: 3 prime UTR variant
orthologous variants: 65398941-G-T

http://identifiers.org/hco/18/GRCh38#58481614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65398956-C-A

58481614-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: 3 prime UTR variant
orthologous variants: 65398956-C-G

58481614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: 3 prime UTR variant
orthologous variants: 65398956-C-T

http://identifiers.org/hco/18/GRCh38#58481635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65398978-C-A

58481758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: 3 prime UTR variant
orthologous variants: 65399070-G-T

58481774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: 3 prime UTR variant
orthologous variants: 65399086-G-T

58481777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: 3 prime UTR variant
orthologous variants: 65399089-G-A

58481800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 65399113-G-T

58481868-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: synonymous_variant, undefined
orthologous variants: 65399190-T-A

58481868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: synonymous_variant, undefined
orthologous variants: 65399190-T-C

58481868-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: synonymous_variant, undefined
orthologous variants: 65399190-T-G

58481869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: missense_variant, undefined
orthologous variants: 65399191-G-A

58481869-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: missense_variant, undefined
orthologous variants: 65399191-G-C

58481879-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: missense variant
orthologous variants: 65399201-T-G

58481883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: synonymous_variant, undefined
orthologous variants: 65399205-T-C

58481917-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: missense_variant, undefined
orthologous variants: 65399239-T-G

58482030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: synonymous variant
orthologous variants: 65399352-T-C

http://identifiers.org/hco/18/GRCh38#58482068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65399400-C-A

58482068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65399400-C-T

58482073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65399405-A-G

58482119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65399450-A-G

58482119-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65399450-A-T

58482131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65399462-G-A

58482131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65399462-G-T

58482144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65399475-A-G

58482169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65399500-G-A

58482169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65399500-G-T

58482502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65400105-A-G

58482593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65400191-C-T

http://identifiers.org/hco/18/GRCh38#58482627-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65400224-C-A

58482676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65400261-A-G

58482932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65400960-G-A

58486728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65402391-A-G

58486733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65402396-G-T

58486877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65402534-C-T

58487191-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65402844-T-G

58487208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65402861-A-G

58487307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65402959-A-G

58492453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65403859-C-T

58492562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65403971-G-A

58492584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65403992-A-G

58492664-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65404033-T-G

58492951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65404348-C-T

58493261-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65404622-C-G

58493335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65404699-T-C

58493466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65404821-T-C

58493664-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65405014-G-C

58493775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65405107-C-T

58493779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65405111-G-T

58493958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, undefined
orthologous variants: 65405302-G-T

58494675-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65405885-T-A

58494785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65405975-G-A

http://identifiers.org/hco/18/GRCh38#58494954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65406187-C-A

58495177-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65406438-T-A

58495241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65406501-G-A

58495316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65406614-G-A

58495394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65406672-A-G

58495709-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65407085-C-G

http://identifiers.org/hco/18/GRCh38#58495712-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65407088-A-C

58495712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65407088-A-G

58495741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65407205-C-T

58495794-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65407258-A-T

58495807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65407271-G-A

58495950-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65407376-C-G

58496074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65407490-A-G

58496074-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65407490-A-T

58496076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65407492-G-T

58496092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65407508-T-C

58496422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65407843-A-G

58496448-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65407882-C-G

58496448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65407882-C-T

58497750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65409419-A-G

58497783-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65409456-T-A

http://identifiers.org/hco/18/GRCh38#58497931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65409612-C-A

58497931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65409612-C-T

58497932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65409613-G-A

58497932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65409613-G-T

http://identifiers.org/hco/18/GRCh38#58497980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65409660-C-A

58497990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65409670-C-T

58498012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65409680-G-T

58498164-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65409833-T-A

58498180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65409861-G-A

58498180-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65409861-G-C

58498180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65409861-G-T

http://identifiers.org/hco/18/GRCh38#58498187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65409868-C-A

58498187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65409868-C-T

http://identifiers.org/hco/18/GRCh38#58498222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65409899-C-A

58498222-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65409899-C-G

58498222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65409899-C-T

http://identifiers.org/hco/18/GRCh38#58498246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65409924-C-A

58498274-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65409952-T-G

58498415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65410025-G-T

58498427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65410037-G-A

58499069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65410247-G-A

58499402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65410569-G-A

58499540-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65410710-C-G

58499540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65410710-C-T

58500176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65411204-G-A

58500191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65411219-A-G

58500191-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65411219-A-T

58500233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65411268-G-A

58500233-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65411268-G-T

58500277-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65411297-C-G

58500322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65411342-C-T

58500344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65411364-A-G

http://identifiers.org/hco/18/GRCh38#58500476-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65411594-A-C

58500830-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65411752-G-C

58500857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65411776-A-G

58500857-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65411776-A-T

58501247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, undefined
orthologous variants: 65412099-G-T

58501874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65412774-T-C

58503806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65413815-G-A

58503806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65413815-G-T

58503925-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65413943-C-G

58503925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65413943-C-T

http://identifiers.org/hco/18/GRCh38#58504007-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65414025-A-C

58504025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: synonymous variant
orthologous variants: 65414043-C-T

58504046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: synonymous variant
orthologous variants: 65414064-A-G

58504109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: synonymous variant
orthologous variants: 65414127-A-G

58504190-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65414208-T-A

http://identifiers.org/hco/18/GRCh38#58504244-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65414256-A-C

58504244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65414256-A-G

58504244-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65414256-A-T

58512019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 65415978-C-T

58512106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 65416068-T-C

58512168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 65416117-C-T

58512178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 65416123-T-C

58512261-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 65416207-G-C

58512421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65416362-T-C

58512459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65416396-G-A

58512459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65416396-G-T

58512465-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65416402-C-G

58512465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65416402-C-T

58512493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65416443-G-A

58513303-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65416564-G-C

58513335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65416595-A-G

58513394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65416651-A-G

58513431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65416688-T-C

58513486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65416747-T-C

http://identifiers.org/hco/18/GRCh38#58514098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65417935-C-A

58514158-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65417999-T-A

58514159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65418000-G-A

58514207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65418070-T-C

58514224-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65418079-C-G

58514238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65418093-T-C

58514249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65418100-T-C

58514577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65418392-A-G

58514582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65418397-G-A

58514613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65418425-G-A

58514623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65418435-A-G

58514646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65418458-T-C

58514660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65418472-A-G

58514833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65422593-A-G

http://identifiers.org/hco/18/GRCh38#58514858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65422617-C-A

58514858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65422617-C-T

58514866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65422625-C-T

58514921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65422676-T-C

http://identifiers.org/hco/18/GRCh38#58514926-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65422681-A-C

58514926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65422681-A-G

58514926-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65422681-A-T

58514959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65422714-G-A

58514959-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65422714-G-T

58515089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 65422845-G-A

58515089-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 65422845-G-T

http://identifiers.org/hco/18/GRCh38#58515133-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65422886-A-C

58515133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65422886-A-G

http://identifiers.org/hco/18/GRCh38#58515150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65422903-C-A

58515158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65422908-G-A

58515177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65422927-A-G

58515241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65423025-A-G

58515330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65423178-T-C

58515330-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65423178-T-G

58515647-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65423515-T-G

58515739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65423612-C-T

58516318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65423827-C-T

58516405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65423904-T-C

58516528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65424004-G-A

http://identifiers.org/hco/18/GRCh38#58516577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65424051-C-A

58516577-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65424051-C-G

58516773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65424195-A-G

58516893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65424312-G-A

58516893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65424312-G-T

58517070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: synonymous variant
orthologous variants: 65424489-T-C

58517103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: synonymous variant
orthologous variants: 65424522-A-G

58517189-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 65424608-C-G

58517290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65424700-G-A

58517290-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65424700-G-C

58517290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65424700-G-T

http://identifiers.org/hco/18/GRCh38#58517296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65424706-C-A

58517296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65424706-C-T

58517316-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65424726-T-A

http://identifiers.org/hco/18/GRCh38#58517334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65424743-C-A

58517334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65424743-C-T

58517400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65424829-A-G

58517453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65424881-C-T

58517520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65424939-G-A

58518360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65425869-G-A

58519582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65426159-A-G

58520023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65426483-T-C

58520081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65426541-G-A

58520094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65426554-C-T

58520102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65426562-A-G

58520119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65426576-G-A

58523711-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65427062-C-G

58523788-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65427134-C-G

58524248-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65427587-C-G

58524248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65427587-C-T

http://identifiers.org/hco/18/GRCh38#58524522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65427882-C-A

58524541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65427922-G-A

58524783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65428200-G-A

http://identifiers.org/hco/18/GRCh38#58524796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65428213-C-A

58524804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65428221-T-C

58525106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65428433-A-G

58525335-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65428683-G-C

58525547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65428891-C-T

58525665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65429009-T-C

58525885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65429179-C-T

58525960-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65429232-T-A

58525960-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65429232-T-G

58526031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65429328-G-A

58526175-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65429519-G-C

58526515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65429769-C-T

58526516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65429770-G-T

58526523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65429777-G-A

58526574-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, undefined
orthologous variants: 65429828-C-G

58526609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65429863-G-T

58526867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65430180-G-A

58527047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65430477-C-T

58527257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65431045-G-A

58527273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65431061-C-T

http://identifiers.org/hco/18/GRCh38#58527371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65431147-C-A

58527441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65431205-C-T

58527469-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65431211-A-T

58527523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65431264-A-G

58527582-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65431321-G-C

58527650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65431382-T-C

58527729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65431461-T-C

58527902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65431631-T-C

58528638-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65432067-T-A

58528638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65432067-T-C

http://identifiers.org/hco/18/GRCh38#58528642-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65432071-A-C

58528642-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65432071-A-T

58528647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65432076-G-A

58528647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65432076-G-T

58528729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65432170-A-G

http://identifiers.org/hco/18/GRCh38#58528731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65432172-C-A

58528731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65432172-C-T

http://identifiers.org/hco/18/GRCh38#58529100-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65433094-A-C

58529138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65433132-A-G

58529264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65433255-G-A

58529617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65433555-A-G

58529919-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65433933-T-A

58529920-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65433934-A-T

http://identifiers.org/hco/18/GRCh38#58529941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#65433955-C-A

58529980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65433981-C-T

58529988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65433989-C-T

58530121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65434103-A-G

58530309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65434288-A-G

58530337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65434316-C-T

http://identifiers.org/hco/18/GRCh38#58531478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65434788-C-A

58531511-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65434830-T-G

http://identifiers.org/hco/18/GRCh38#58531521-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65434840-A-C

58531521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65434840-A-G

58531553-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65434859-T-A

58531577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65434880-G-A

58531577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65434880-G-T

http://identifiers.org/hco/18/GRCh38#58531624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65434936-C-A

58531624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65434936-C-T

58531990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65434986-C-T

58532167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65435149-G-T

58532282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65435235-A-G

58532315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65435258-A-G

58533003-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65436057-G-T

58533010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65436064-G-A

58533583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65436463-T-C

58533829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65436619-G-A

http://identifiers.org/hco/18/GRCh38#58534104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65436874-C-A

58534104-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65436874-C-G

58534214-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65436934-G-C

http://identifiers.org/hco/18/GRCh38#58534338-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65437025-A-C

58534345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65437037-A-G

58534410-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65437095-T-G

58534415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65437100-G-A

58534425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65437110-A-G

58534626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65437315-C-T

58534822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65437511-A-G

58534907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65437594-T-C

58535071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65437755-T-C

http://identifiers.org/hco/18/GRCh38#58535100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65437784-C-A

58535147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65437834-A-G

58535188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65437884-T-C

58535189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65437885-A-G

58535273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65437969-C-T

58535327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65438023-G-T

58535337-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65438033-T-A

58535409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65438105-T-C

http://identifiers.org/hco/18/GRCh38#58535454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65438150-C-A

58535454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65438150-C-T

58535456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65438152-C-T

58535464-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65438160-G-C

58535464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65438160-G-T

58535532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65438213-G-A

58535545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65438226-T-C

58535611-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65438292-G-C

58535718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65438399-G-A

58535718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65438399-G-T

58535750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 65438429-A-G

58535750-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 65438429-A-T

58535768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 65438461-G-A

58535844-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65438546-T-G

58535928-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65438618-G-C

58535928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65438618-G-T

http://identifiers.org/hco/18/GRCh38#58535965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: http://identifiers.org/mco/18/GRCm39#65438655-C-A

58535965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65438655-C-T

58536015-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65438705-T-G

http://identifiers.org/hco/18/GRCh38#58536098-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65438788-A-C

58536098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 65438788-A-G

58536098-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 65438788-A-T

http://identifiers.org/hco/18/GRCh38#58536260-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65438950-A-C

58536260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65438950-A-G

58536305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65438998-T-C

58536344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65439037-T-C

58536362-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65439055-T-A

58536372-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65439065-A-T

58536620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 65439313-C-T

58536628-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65439321-A-T

58536738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65439431-G-A

58536738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65439431-G-T

58536773-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65439466-C-G

58536883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 65439576-G-A

58536883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65439576-G-T

58536891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65439581-G-A

58536942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65439629-A-G

http://identifiers.org/hco/18/GRCh38#58536951-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65439638-A-C

58536951-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65439638-A-T

58536979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65439666-T-C

58537002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65439689-C-T

58537006-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65439693-A-T

58537065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65439761-G-A

58537076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65439772-C-T

58537113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65439809-A-G

58537113-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65439809-A-T

58537120-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65439816-G-C

58537120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65439816-G-T

58537139-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65439835-T-A

58537139-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65439835-T-G

http://identifiers.org/hco/18/GRCh38#58537243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65439933-C-A

http://identifiers.org/hco/18/GRCh38#58537282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65439972-C-A

58537282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65439972-C-T

58537415-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65440081-T-G

58537416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65440082-G-A

58537416-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65440082-G-C

58537489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65440155-G-A

58537502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65440168-G-A

58537524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65440190-G-A

http://identifiers.org/hco/18/GRCh38#58537568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65440234-C-A

58537568-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65440234-C-G

58537568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65440234-C-T

58537678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65440338-A-G

58537844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65440504-G-A

58537932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65440592-G-A

58537932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65440592-G-T

58537935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65440595-A-G

58537935-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65440595-A-T

58537959-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65440619-A-T

58537971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65440631-T-C

58537971-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65440631-T-G

58537975-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 65440635-T-A

58538063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65440723-C-T

58538064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65440724-G-A

58538114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65440774-G-A

58538114-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65440774-G-C

58538135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65440795-A-G

58538254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65440913-A-G

58538292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65440951-A-G

58538292-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65440951-A-T

58538357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65441028-A-G

58538387-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65441058-T-G

58538508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65441178-G-T

58538624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65441285-C-T

58538648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65441310-C-T

58539717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65442147-T-C

58539720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65442156-A-G

58539720-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65442156-A-T

58539801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65442227-A-G

http://identifiers.org/hco/18/GRCh38#58539875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65442297-C-A

58540024-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65442411-T-G

58540114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65442508-G-A

58540160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65442554-G-A

58540362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65442828-G-A

58540362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65442828-G-T

58540384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65442905-C-T

58540594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65443197-T-C

58541874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65445235-G-A

58542440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65445755-C-T

58542457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65445771-A-G

58542557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65445874-A-G

58542569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65445886-T-C

http://identifiers.org/hco/18/GRCh38#58542772-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65446078-A-C

58542772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65446078-A-G

58542784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65446090-G-A

58542832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65446128-G-T

58542887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65446181-G-T

58543921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65447177-G-A

58543973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65447226-A-G

58544119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65447362-A-G

58544130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65447373-G-T

58544192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65447439-T-C

58544338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65447543-A-G

58544394-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65447598-T-G

58544579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65447769-T-C

58544581-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65447771-G-C

58544587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65447777-T-C

58544587-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65447777-T-G

http://identifiers.org/hco/18/GRCh38#58544657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65447821-C-A

58544665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 65447824-C-T

58544742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65447901-C-T

58544755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65447914-T-C

58544816-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65447965-T-G

58544822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65447971-A-G

58544871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65448018-A-G

58544908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65448059-T-C

http://identifiers.org/hco/18/GRCh38#58544913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65448064-C-A

58544946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65448096-G-T

58544962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65448112-A-G

58544968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65448118-G-T

58544973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65448123-A-G

http://identifiers.org/hco/18/GRCh38#58544985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65448135-C-A

58544985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65448135-C-T

58545012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 65448792-A-G

58545020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65448801-T-C

58545033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65448814-T-C

58545055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65448833-C-T

58545064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65448842-G-A

http://identifiers.org/hco/18/GRCh38#58545111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65448890-C-A

58545111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65448890-C-T

http://identifiers.org/hco/18/GRCh38#58545292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65449028-C-A

58545292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65449028-C-T

58545363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65449086-T-C

58545520-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65449243-G-C

58545657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65449364-G-A

http://identifiers.org/hco/18/GRCh38#58545666-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65449376-C-A

58545814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65449522-G-A

58545814-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65449522-G-C

58545917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65449589-C-T

58545929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65449601-C-T

http://identifiers.org/hco/18/GRCh38#58545951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65449623-C-A

58545951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65449623-C-T

58546075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65449747-C-T

http://identifiers.org/hco/18/GRCh38#58546149-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65449818-A-C

58546478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65450166-G-A

58546579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65450263-C-T

58546605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65450289-T-C

58546803-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65451187-C-G

58546963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65451318-G-T

58547002-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65451351-T-A

58547002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65451351-T-C

58547002-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65451351-T-G

58547009-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65451358-A-T

58547462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65451709-C-T

http://identifiers.org/hco/18/GRCh38#58547600-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65451839-A-C

58548085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65452280-A-G

58548085-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65452280-A-T

58548145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65452343-C-T

58548290-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65452458-A-T

58548607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65452682-C-T

58548612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65452687-C-T

58548613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65452688-G-A

58549096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65452957-G-A

58549286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65453151-A-G

58549549-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65453587-T-A

58549549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65453587-T-C

58549575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65453611-G-A

58549677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65453707-A-G

58550097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65454075-A-G

58550140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65454140-T-C

58550996-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65454319-C-G

58551084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65454393-T-C

58551116-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65454429-A-T

58551226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65454526-A-G

58551282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65454580-C-T

58551423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65454720-G-A

58551425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65454722-G-T

58551464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65454758-T-C

58551597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65454913-C-T

58551936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65455209-G-A

58555270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65460107-T-C

58555292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65460131-A-G

58555420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65460261-T-C

58555485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65460319-A-G

http://identifiers.org/hco/18/GRCh38#58556270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65461561-C-A

58556536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65461822-G-A

58556536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65461822-G-T

58556843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65462102-G-A

58556843-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65462102-G-C

http://identifiers.org/hco/18/GRCh38#58556926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65462189-C-A

58556926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65462189-C-T

58557219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65462488-A-G

58557222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65462492-G-T

58557229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65462500-G-A

58557229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65462500-G-T

http://identifiers.org/hco/18/GRCh38#58557235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#65462505-C-A

http://identifiers.org/hco/18/GRCh38#58557279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#65462548-C-A

58557279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65462548-C-T

58557288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65462558-C-T

http://identifiers.org/hco/18/GRCh38#58557391-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#65462650-A-C

58557391-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65462650-A-T

http://identifiers.org/hco/18/GRCh38#58557777-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65463064-A-C

http://identifiers.org/hco/18/GRCh38#58557941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65463231-C-A

58558067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65463358-G-A

58558072-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65463363-T-A

58558111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65463412-A-G

58558181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65463480-C-T

58558759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65464019-T-C

58558829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65464078-C-T

http://identifiers.org/hco/18/GRCh38#58558847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65464093-C-A

58558847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65464093-C-T

58558918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65464162-G-A

58559024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65464218-G-A

58559048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65464243-A-G

http://identifiers.org/hco/18/GRCh38#58559070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65464264-C-A

http://identifiers.org/hco/18/GRCh38#58559083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65464277-C-A

58559154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65464355-A-G

58559165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65464366-G-A

58559165-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65464366-G-T

58559335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65464525-C-T

58559336-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65464526-A-T

58559355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65464546-G-A

58559356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65464547-T-C

58559572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65464724-C-T

58559617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65464768-G-A

http://identifiers.org/hco/18/GRCh38#58559701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65464840-C-A

58559724-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65464849-G-C

58559741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65464866-G-A

58559766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65464890-C-T

58559882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65464962-T-C

58559936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65465022-C-T

58559940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65465026-A-G

58560686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65465582-G-A

58560730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65465617-G-A

58560990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65466181-T-C

http://identifiers.org/hco/18/GRCh38#58561472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65466844-C-A

58561472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65466844-C-T

58561476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65466848-C-T

58561534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65466939-C-T

58561799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65467173-G-T

58561890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65467247-G-A

58562065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65467404-T-C

58562112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65467450-G-T

58562257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65467520-G-T

58563826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65467891-G-A

58563870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65467931-A-G

58563885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65467946-A-G

http://identifiers.org/hco/18/GRCh38#58563956-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65468019-A-C

58566219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65471651-G-A

http://identifiers.org/hco/18/GRCh38#58566388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65471820-C-A

http://identifiers.org/hco/18/GRCh38#58566397-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65471829-A-C

http://identifiers.org/hco/18/GRCh38#58566483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65471915-C-A

58566483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65471915-C-T

58566526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65471967-C-T

58566566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65472013-G-A

58566566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65472013-G-T

http://identifiers.org/hco/18/GRCh38#58566598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65472036-C-A

58566618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65472056-C-T

http://identifiers.org/hco/18/GRCh38#58566847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65472221-C-A

58566862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65472240-G-A

58569325-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65473153-C-G

58569325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65473153-C-T

58569566-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65473492-C-G

58569566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65473492-C-T

http://identifiers.org/hco/18/GRCh38#58569814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65473730-C-A

58570370-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65473910-A-T

58570436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65473978-C-T

http://identifiers.org/hco/18/GRCh38#58570540-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#65474068-A-C

58570589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65474108-G-T

58574808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65479133-G-A

58575218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65479211-A-G

58575395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65479369-A-G

58576418-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65480064-T-G

58576503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65480146-G-T

58576536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65480177-G-A

58576893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65480538-G-A

58576902-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65480547-G-C

58576907-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65480554-G-C

58576907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65480554-G-T

58576917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65480564-C-T

58577063-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65480672-T-A

http://identifiers.org/hco/18/GRCh38#58577065-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65480674-A-C

58577088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65480687-A-G

58577175-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65480771-G-C

http://identifiers.org/hco/18/GRCh38#58577228-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65480808-C-A

58577250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65480818-G-A

58577995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65481282-C-T

58578317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65481605-G-A

58578317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65481605-G-T

http://identifiers.org/hco/18/GRCh38#58578330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65481619-C-A

58578352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65481641-G-T

58578409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65481698-T-C

58578410-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65481699-T-A

58578410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65481699-T-C

http://identifiers.org/hco/18/GRCh38#58578415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65481704-C-A

58578415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65481704-C-T

http://identifiers.org/hco/18/GRCh38#58578479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65481768-C-A

58578601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65481889-G-T

58578663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65481957-T-C

58578744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65482031-A-G

58578760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65482047-A-G

58578760-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65482047-A-T

http://identifiers.org/hco/18/GRCh38#58578786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65482073-C-A

58578786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65482073-C-T

58578787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65482074-G-A

58578787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65482074-G-T

58578886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 65482171-G-A

58578974-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 65482256-T-A

58579135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65482408-C-T

58579157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65482430-G-A

58579157-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65482430-G-C

58579165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65482438-C-T

http://identifiers.org/hco/18/GRCh38#58579213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#65482486-C-A

58579243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65482516-A-G

58579252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65482525-C-T

58579284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65482557-G-A

58579284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65482557-G-T

58579411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 65482684-G-A

58579411-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 65482684-G-C

58579438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65482711-C-T

58579545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65482818-C-T

58579555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65482828-G-A

58579555-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65482828-G-C

58579664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65482937-A-G

58579807-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 65483080-T-G

58579993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65483266-C-T

58580029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65483299-A-G

58580114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65483384-C-T

58580189-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: missense variant
orthologous variants: 65483444-G-T

58580240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: missense_variant, undefined
orthologous variants: 65483495-T-C

58580348-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65483582-T-A

58580417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65483651-T-C

http://identifiers.org/hco/18/GRCh38#58580512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65483743-C-A

58580512-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65483743-C-G

58580512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65483743-C-T

58580532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65483763-C-T

58580536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65483767-A-G

http://identifiers.org/hco/18/GRCh38#58581450-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#65484330-A-C

58581950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65484833-A-G

58582094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65484945-C-T

58582169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65485002-T-C

58583801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65485871-G-A

58583880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65485933-T-C

58583953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65486001-G-T

58584107-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65486241-A-T

58584261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65486375-T-C

58584602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65486841-T-C

58584880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, undefined
orthologous variants: 65487105-G-A

58584915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, undefined
orthologous variants: 65487141-G-A

58585093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65487538-G-A

58585229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65487677-T-C

58585230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65487678-A-G

58585365-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65487801-T-G

58585447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65487886-G-T

58588087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65488671-G-A

58588273-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65488852-C-G

58588273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65488852-C-T

58588465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65488977-T-C

58589209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65489465-A-G

58589210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65489466-T-C

58589256-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65489511-C-G

58589261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65489516-G-A

58589261-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65489516-G-T

58590422-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65490099-C-G

58590422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65490099-C-T

58590472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65490151-G-T

58590516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65490195-G-A

58590519-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65490198-T-G

58591387-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65491261-G-C

58591476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65491357-G-A

58591497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65491378-A-G

58591528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65491413-G-A

58591545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65491462-G-A

58591936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65492195-G-A

58592288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65492537-A-G

58592710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65492906-T-C

http://identifiers.org/hco/18/GRCh38#58592711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65492907-C-A

58592711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65492907-C-T

http://identifiers.org/hco/18/GRCh38#58595132-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65493319-C-A

58595296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65493483-C-T

58595446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65493658-C-T

58595478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65493749-G-A

58595876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65494363-T-C

58596148-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65494698-A-T

58596263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65494911-A-G

58596265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65494913-G-A

58596455-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65495094-C-G

58596473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65495113-C-T

http://identifiers.org/hco/18/GRCh38#58596524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65495159-C-A

58596570-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65495219-G-C

58596585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65495234-G-A

58599116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, undefined
orthologous variants: 65498106-G-A

58599248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65498233-C-T

58599265-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65498251-T-A

58600498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65499165-G-A

58600498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65499165-G-T

58600538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, undefined
orthologous variants: 65499208-G-T

58603211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65501596-C-T

58603236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65501629-A-G

58603251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65501637-C-T

58603290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65501676-G-A

58603339-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65501722-C-G

http://identifiers.org/hco/18/GRCh38#58603579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#65501923-C-A

58603601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, undefined
orthologous variants: 65501946-A-G

58603602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, undefined
orthologous variants: 65501947-A-G

58603704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65502011-G-A

58603751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65502061-A-G

58603924-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65502222-C-G

58603924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65502222-C-T

58603939-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65502237-T-A

58603940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65502238-G-T

http://identifiers.org/hco/18/GRCh38#58604106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65502721-C-A

58604203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65502809-T-C

58605601-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, undefined
orthologous variants: 65503073-A-T

58605610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, undefined
orthologous variants: 65503082-G-A

58605679-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, undefined
orthologous variants: 65503147-T-G

http://identifiers.org/hco/18/GRCh38#58605702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#65503168-C-A

58605702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron_variant, undefined
orthologous variants: 65503168-C-T

58606683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65504453-A-G

58606683-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65504453-A-T

http://identifiers.org/hco/18/GRCh38#58607266-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65505737-C-A

58607266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65505737-C-T

58607283-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65505753-G-C

58607283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65505753-G-T

58607295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65505765-A-G

http://identifiers.org/hco/18/GRCh38#58607300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65505770-C-A

58607300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65505770-C-T

58607448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65505918-A-G

58607497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65505966-A-G

58607507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65505978-A-G

58607531-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65506013-T-A

58608273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65508420-T-C

58608350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65508500-G-T

58608615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65508759-G-A

58608895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65508819-T-C

58609279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65509053-C-T

58609467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65509230-C-T

58609503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65509269-G-A

58609503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65509269-G-T

58609534-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65509298-T-G

58609969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65509779-C-T

58610505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65510413-G-T

http://identifiers.org/hco/18/GRCh38#58610568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65510480-C-A

58610590-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65510499-T-A

58610646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65510553-A-G

58611490-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65510832-T-G

58611508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65510847-T-C

58611583-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65510905-C-G

58611644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65510963-G-T

58611711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: synonymous variant
orthologous variants: 65511109-A-G

58611908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65511302-G-A

58611908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65511302-G-T

58611957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65511350-G-A

58611957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65511350-G-T

58611965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65511358-A-G

58612164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65511514-C-T

58612614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65512155-G-A

58612729-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65512238-C-G

58612753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65512255-C-T

58612849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65512351-C-T

58612883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65512377-C-T

58613911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65512993-C-T

58614010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65513079-C-T

58614128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65513183-T-C

58614141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65513196-G-A

58614192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65513247-A-G

58614216-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65513258-A-T

58614396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65513411-A-G

58614400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65513415-G-A

58614563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65513561-G-A

58615232-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65514457-T-A

58615253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65514477-G-A

http://identifiers.org/hco/18/GRCh38#58615420-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65514620-A-C

58615554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65514751-C-T

58615689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65514910-T-C

58616046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65515254-A-G

58619037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65516015-C-T

58622765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65520386-G-A

58622842-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65520459-C-G

58623831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65521123-A-G

58624182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65522125-A-G

58624398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65522374-A-G

http://identifiers.org/hco/18/GRCh38#58625177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65523044-C-A

58625200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65523060-G-A

58625510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65523335-G-A

58625809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65523584-C-T

58626243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65524511-C-T

58626572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65524848-C-T

58626919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65525269-A-G

http://identifiers.org/hco/18/GRCh38#58626991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65525341-C-A

http://identifiers.org/hco/18/GRCh38#58627872-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65525871-A-C

http://identifiers.org/hco/18/GRCh38#58628155-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#65526167-A-C

58628194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65526203-A-G

58628419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65526375-A-G

58628604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65526561-A-G

58628678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: intron variant
orthologous variants: 65526620-T-C

58628788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: 5 prime UTR variant
orthologous variants: 65526729-A-G

58628809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: 5 prime UTR variant
orthologous variants: 65526750-A-G

58628810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: 5 prime UTR variant
orthologous variants: 65526751-G-A

58628838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: 5 prime UTR variant
orthologous variants: 65526779-G-A

58628838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20565
most severe consequence: 5 prime UTR variant
orthologous variants: 65526779-G-T