113751336-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: 5 prime UTR variant
orthologous variants: 56449728-G-T

113751406-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 56449797-T-G

113751427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 56449818-T-C

113751454-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 56449848-A-T

113751552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 56449943-T-C

113751609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 56449996-A-G

113751771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56450140-G-A

113751771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56450140-G-T

113751772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56450141-C-T

113751803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56450175-G-A

http://identifiers.org/hco/10/GRCh38#113755237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56452962-C-A

113755316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 56453039-G-A

http://identifiers.org/hco/10/GRCh38#113755339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56453062-C-A

113755339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 56453062-C-T

113763322-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56456231-G-C

113763375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56456285-C-T

113763622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56456639-G-A

113763672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56456699-A-G

113763776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56456802-A-G

113763933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56456959-C-T

113764099-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56457106-C-G

113764099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56457106-C-T

113764452-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56457343-T-A

113764484-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56457375-T-G

113764729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56457625-C-T

113764797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56457696-T-C

http://identifiers.org/hco/10/GRCh38#113764929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56457828-C-A

http://identifiers.org/hco/10/GRCh38#113764961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56457856-C-A

113765032-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 56457914-G-T

113765086-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 56457963-T-A

113765086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 56457963-T-C

113765235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 56458091-T-C

113765258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 56458120-T-C

113765458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56458274-A-G

http://identifiers.org/hco/10/GRCh38#113765492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56458328-C-A

113765514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56458375-G-T

http://identifiers.org/hco/10/GRCh38#113765516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56458377-C-A

113765790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56458626-A-G

113765791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56458627-C-T

113765886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56458704-G-T

113765986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56458768-C-T

113765988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56458770-G-A

113766258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56459016-G-A

113766260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56459018-T-C

113766285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56459056-G-A

113766552-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56459312-T-A

113766552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56459312-T-C

113766662-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 56459419-C-G

113766662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 56459419-C-T

http://identifiers.org/hco/10/GRCh38#113766727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56459484-C-A

113766753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56459510-A-G

113766787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56459535-G-A

113766787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56459535-G-T

113766816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56459565-G-A

113766819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56459568-A-G

113766858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56459610-G-A

113766860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56459612-G-A

113766860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56459612-G-T

113766927-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56459676-G-C

113767260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56460050-T-C

113767261-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56460051-A-T

113767303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56460086-T-C

113767303-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56460086-T-G

113767306-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56460094-A-T

113767334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56460123-A-G

113767344-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: splice acceptor variant
orthologous variants: 56460129-G-C

http://identifiers.org/hco/10/GRCh38#113767459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: stop gained
orthologous variants: http://identifiers.org/mco/19/GRCm39#56460244-C-A

113767459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: synonymous variant
orthologous variants: 56460244-C-T

113767564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56460409-A-G

113767565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56460410-T-C

113767568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56460413-T-C

http://identifiers.org/hco/10/GRCh38#113767600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56460461-C-A

113767600-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56460461-C-G

113767712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56460759-T-C

113767806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56460851-G-A

113767885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56460950-T-C

113767925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56460990-G-A

113768000-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56461060-T-G

113768089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56461142-G-A

113768094-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56461147-C-G

113768292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56461335-G-T

113768316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56461359-C-T

113768362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56461390-A-G

http://identifiers.org/hco/10/GRCh38#113768670-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56461468-A-C

113768672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56461471-G-A

http://identifiers.org/hco/10/GRCh38#113768675-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56461474-A-C

113768675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56461474-A-G

113768700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56461500-T-C

113768700-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56461500-T-G

http://identifiers.org/hco/10/GRCh38#113768903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56461709-C-A

113768985-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56461789-T-A

113768985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56461789-T-C

http://identifiers.org/hco/10/GRCh38#113768988-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56461792-C-A

113768988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56461792-C-T

http://identifiers.org/hco/10/GRCh38#113769365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56462169-C-A

http://identifiers.org/hco/10/GRCh38#113769560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56462342-C-A

113769560-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56462342-C-G

113769560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56462342-C-T

http://identifiers.org/hco/10/GRCh38#113769567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56462349-C-A

113769567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56462349-C-T

113769584-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56462366-C-G

113769614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56462396-G-A

113769791-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: missense variant
orthologous variants: 56462580-T-A

113769791-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: missense variant
orthologous variants: 56462580-T-G

http://identifiers.org/hco/10/GRCh38#113769813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56462602-C-A

113769813-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: synonymous variant
orthologous variants: 56462602-C-G

113769845-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: missense variant
orthologous variants: 56462634-C-G

113769860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: missense variant
orthologous variants: 56462649-C-T

113769909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56462698-G-A

113769909-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56462698-G-C

http://identifiers.org/hco/10/GRCh38#113770001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56462815-C-A

113770357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56463434-C-T

113770369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56463443-A-G

113770395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56463469-A-G

113770403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56463477-T-C

113771223-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron variant
orthologous variants: 56465144-A-T

http://identifiers.org/hco/10/GRCh38#113771822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56465417-C-A

113771822-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56465417-C-G

113771850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56465445-T-C

113771905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56465504-A-G

113772108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56465778-T-C

113772155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56465823-A-G

http://identifiers.org/hco/10/GRCh38#113772234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56465905-C-A

113772426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56466063-G-A

113772426-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56466063-G-C

http://identifiers.org/hco/10/GRCh38#113774176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56466805-C-A

113774176-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56466805-C-G

113774197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56466825-G-A

113774197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56466825-G-T

113774271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56466899-A-G

113774316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56466944-T-C

113774336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56466973-A-G

113774364-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56467000-G-T

113774511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56467932-A-G

113774617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56468019-G-A

113774675-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56468078-G-T

http://identifiers.org/hco/10/GRCh38#113774713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56468110-C-A

http://identifiers.org/hco/10/GRCh38#113774715-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56468112-A-C

113774715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56468112-A-G

113774735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56468133-T-C

http://identifiers.org/hco/10/GRCh38#113774738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56468136-C-A

113774738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56468136-C-T

http://identifiers.org/hco/10/GRCh38#113774745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56468153-C-A

113774779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56468187-A-G

113774856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56468264-G-A

113774856-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56468264-G-C

113774856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56468264-G-T

113774859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56468267-T-C

113774859-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56468267-T-G

http://identifiers.org/hco/10/GRCh38#113775165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56468560-C-A

113775165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56468560-C-T

http://identifiers.org/hco/10/GRCh38#113775175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56468568-C-A

113775175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56468568-C-T

113775272-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56468663-T-G

113775295-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56468686-T-A

113775336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56468725-C-T

113775623-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56469309-T-A

113775623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56469309-T-C

113775623-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56469309-T-G

http://identifiers.org/hco/10/GRCh38#113775649-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56469337-A-C

113775649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56469337-A-G

http://identifiers.org/hco/10/GRCh38#113775652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56469340-C-A

113775652-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56469340-C-G

113775727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56469416-G-A

113775870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56469564-G-A

113775870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56469564-G-T

113775908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56469600-G-A

113775985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56469660-G-A

113775985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56469660-G-T

113776082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56469743-A-G

113776372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56469987-G-T

113776813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56470699-T-C

113777006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56470882-G-A

113777006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56470882-G-T

113777013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56470888-G-A

113777013-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56470888-G-C

113777013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56470888-G-T

113777023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56470898-G-T

113777096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56470992-G-A

113777096-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56470992-G-C

http://identifiers.org/hco/10/GRCh38#113777172-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56471066-C-A

113777172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56471066-C-T

113777306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56471200-G-A

113777306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56471200-G-T

113777341-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56471235-G-C

113778085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56471355-G-A

113778085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56471355-G-T

http://identifiers.org/hco/10/GRCh38#113778109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56471380-C-A

113778202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56471464-T-C

113778294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56471617-C-T

113779594-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56472261-T-A

113779675-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56472344-C-G

113779675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56472344-C-T

113779761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56472420-G-A

113779904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56472592-T-C

113780116-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56472984-T-G

113780145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56473014-T-C

113780306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56473131-G-A

http://identifiers.org/hco/10/GRCh38#113780310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56473135-C-A

113780310-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56473135-C-G

113780310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56473135-C-T

113780525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56474024-G-A

113780525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56474024-G-T

http://identifiers.org/hco/10/GRCh38#113780877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56474357-C-A

113780877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56474357-C-T

http://identifiers.org/hco/10/GRCh38#113780902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56474377-C-A

113780902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56474377-C-T

113780910-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56474385-T-A

113780910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56474385-T-C

113780922-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56474396-T-A

113780922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56474396-T-C

113780922-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56474396-T-G

113780944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56474406-A-G

113780944-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56474406-A-T

113780993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56474435-G-T

113781045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56474486-G-T

113781092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56474535-A-G

113781171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56474594-T-C

113781171-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56474594-T-G

http://identifiers.org/hco/10/GRCh38#113781189-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56474606-A-C

113781977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56474683-G-T

113782032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56474726-A-G

113782065-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56474759-C-G

113782108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56474805-G-A

113782108-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56474805-G-C

113782122-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56474818-T-G

113782155-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56474850-G-C

113782259-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56474960-T-G

http://identifiers.org/hco/10/GRCh38#113782341-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56475043-C-A

http://identifiers.org/hco/10/GRCh38#113782350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26285
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56475052-C-A