26021705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134099929-A-G

26021732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134099902-G-A

http://identifiers.org/hco/1/GRCh38#26021773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#134099859-C-A

26021773-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134099859-C-G

26021773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134099859-C-T

26021776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134099856-G-A

26021776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134099856-G-T

26021872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134099749-T-C

26021874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134099747-G-A

26021874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134099747-G-T

26022115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134099555-C-T

26022148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134099508-G-A

26022148-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134099508-G-T

http://identifiers.org/hco/1/GRCh38#26022151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#134099505-C-A

26022151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134099505-C-T

26022301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134099353-T-C

26022304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134099350-A-G

http://identifiers.org/hco/1/GRCh38#26022401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#134099257-C-A

http://identifiers.org/hco/1/GRCh38#26022578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#134099094-C-A

26022578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134099094-C-T

26022748-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 134098935-G-C

26022748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 134098935-G-T

26022961-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 134098722-A-T

26023064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 134098616-G-A

26023247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134098445-C-T

http://identifiers.org/hco/1/GRCh38#26023263-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#134098429-C-A

26023263-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134098429-C-G

26023263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134098429-C-T

http://identifiers.org/hco/1/GRCh38#26023286-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#134098406-C-A

http://identifiers.org/hco/1/GRCh38#26023292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#134098400-C-A

26023292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134098400-C-T

http://identifiers.org/hco/1/GRCh38#26023547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#134098141-C-A

26023547-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134098141-C-G

http://identifiers.org/hco/1/GRCh38#26023552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#134098136-C-A

26023552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134098136-C-T

26023564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134098127-G-T

26023617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134098072-G-T

26023796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134097423-A-G

http://identifiers.org/hco/1/GRCh38#26023861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#134097365-C-A

26024148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134097097-G-A

http://identifiers.org/hco/1/GRCh38#26024219-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#134097061-A-C

26024375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134096962-T-C

26024491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134096850-G-A

26024510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134096826-C-T

26024523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134096813-C-T

26024549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134096789-C-T

26025298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134095876-G-T

26026456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134094250-G-A

26026759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134093942-C-T

26026837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134093864-G-A

26027338-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134093573-T-G

26027361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134093559-T-C

26027363-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134093557-G-C

26028275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134093106-C-T

26028496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134092932-G-A

26028592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134092845-T-C

http://identifiers.org/hco/1/GRCh38#26028664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#134092785-C-A

26028784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 134092667-G-A

26028874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134092548-C-T

26028952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134092483-G-A

26029095-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134092367-G-C

26029095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134092367-G-T

26029302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134092192-G-A

26029302-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134092192-G-C

26029302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134092192-G-T

26029355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134092141-G-T

26029503-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134092085-T-A

26029561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134092032-G-T

http://identifiers.org/hco/1/GRCh38#26029612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#134091985-C-A

26029612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134091985-C-T

http://identifiers.org/hco/1/GRCh38#26029699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#134091898-C-A

26029699-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134091898-C-G

26029699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134091898-C-T

26029859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134091781-G-A

26029859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134091781-G-T

26029860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134091780-C-T

26029874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134091767-G-T

26030142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134091592-T-C

26030455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134090533-T-C

26030461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134090527-C-T

26030462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134090526-C-T

http://identifiers.org/hco/1/GRCh38#26030463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#134090525-C-A

26030463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134090525-C-T

http://identifiers.org/hco/1/GRCh38#26031012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#134090135-C-A

26031019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134090128-T-C

26031019-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134090128-T-G

http://identifiers.org/hco/1/GRCh38#26031052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#134090109-C-A

26031115-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134090043-C-G

26031116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134090042-T-C

26031117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134090041-T-C

26031130-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 134090026-A-T

http://identifiers.org/hco/1/GRCh38#26031144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#134090012-C-A

26031144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 134090012-C-T

26031276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134089880-G-A

http://identifiers.org/hco/1/GRCh38#26031278-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#134089878-A-C

26031278-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134089878-A-T

http://identifiers.org/hco/1/GRCh38#26031325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#134089829-C-A

26031325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134089829-C-T

http://identifiers.org/hco/1/GRCh38#26031395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#134089776-C-A

26031395-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134089776-C-G

26031395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134089776-C-T

http://identifiers.org/hco/1/GRCh38#26031409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#134089762-C-A

26031411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134089760-T-C

http://identifiers.org/hco/1/GRCh38#26031487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#134089689-C-A

26031514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 134089662-A-G

http://identifiers.org/hco/1/GRCh38#26031551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#134089625-C-A

26031551-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 134089625-C-G

26031551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 134089625-C-T

26031571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron variant
orthologous variants: 134089605-G-A

26031571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron variant
orthologous variants: 134089605-G-T

http://identifiers.org/hco/1/GRCh38#26031591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#134089585-C-A

26031591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron variant
orthologous variants: 134089585-C-T

http://identifiers.org/hco/1/GRCh38#26031599-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#134089577-C-A

26031602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron variant
orthologous variants: 134089574-G-A

26031602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron variant
orthologous variants: 134089574-G-T

http://identifiers.org/hco/1/GRCh38#26031657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#134089540-C-A

http://identifiers.org/hco/1/GRCh38#26031770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#134089425-C-A

26031942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron variant
orthologous variants: 134089221-C-T

26032354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 134087970-G-T

26032367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 134087958-G-A

26032367-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 134087958-G-C

26032388-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 134087938-T-G

26032391-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 134087935-T-A

26032420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 134087906-A-G

26032420-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 134087906-A-T

26032422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 134087904-G-A

26032422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 134087904-G-T

26032469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 134087857-T-C

26032477-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 134087849-C-G

26032477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 134087849-C-T

http://identifiers.org/hco/1/GRCh38#26032520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#134087822-C-A

http://identifiers.org/hco/1/GRCh38#26032532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#134087810-C-A

26032532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134087810-C-T

26032608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134087739-A-G

26032622-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134087725-G-T

26032645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134087618-C-T

26032739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134087526-A-G

26032755-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134087511-T-A

http://identifiers.org/hco/1/GRCh38#26032784-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#134087482-A-C

http://identifiers.org/hco/1/GRCh38#26032833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#134087423-C-A

26033134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134087252-C-T

http://identifiers.org/hco/1/GRCh38#26033341-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#134087032-C-A

http://identifiers.org/hco/1/GRCh38#26033354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#134087020-C-A

26033354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134087020-C-T

http://identifiers.org/hco/1/GRCh38#26033389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#134086985-C-A

26033389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134086985-C-T

http://identifiers.org/hco/1/GRCh38#26033425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#134086966-C-A

26033425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134086966-C-T

26033430-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134086961-T-A

http://identifiers.org/hco/1/GRCh38#26033573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#134086674-C-A

26033573-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134086674-C-G

26033573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134086674-C-T

26033753-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 134086497-A-T

26033816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 134086434-G-A

26033863-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 134086387-A-T

26033866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134086379-C-T

26033871-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134086374-C-G

26033874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134086371-G-A

http://identifiers.org/hco/1/GRCh38#26033914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#134086329-C-A

26033914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134086329-C-T

http://identifiers.org/hco/1/GRCh38#26034688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#134085602-C-A

26034688-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134085602-C-G

26034688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134085602-C-T

26034710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134085580-T-C

26034710-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134085580-T-G

26034722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134085565-G-A

26034776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134085513-A-G

26035076-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron variant
orthologous variants: 134085222-T-G

26035118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron variant
orthologous variants: 134085185-C-T

26035120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron variant
orthologous variants: 134085183-G-A

26035120-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron variant
orthologous variants: 134085183-G-C

26035136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: intron variant
orthologous variants: 134085168-C-T

26035170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: synonymous variant
orthologous variants: 134085134-T-C

http://identifiers.org/hco/1/GRCh38#26035178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#134085126-C-A

26035178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: missense variant
orthologous variants: 134085126-C-T

26035201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: missense variant
orthologous variants: 134085103-G-T

26035347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: stop_retained_variant, undefined
orthologous variants: 134084957-G-A

26035347-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: stop_lost, undefined
orthologous variants: 134084957-G-C

26035459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 134084912-G-T

http://identifiers.org/hco/1/GRCh38#26035478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#134084894-C-A

26035478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 134084894-C-T

26035503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 134084860-G-A

26035503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 134084860-G-T

26035523-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 134084842-T-A

26035523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 134084842-T-C

26035523-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 134084842-T-G

http://identifiers.org/hco/1/GRCh38#26035529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#134084829-C-A

26035529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 134084829-C-T

26035539-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 134084813-C-G

26035539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 134084813-C-T

26035554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: 3 prime UTR variant
orthologous variants: 134084797-G-A

26035554-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: 3 prime UTR variant
orthologous variants: 134084797-G-C

26035599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: 3 prime UTR variant
orthologous variants: 134084752-G-A

26035599-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: 3 prime UTR variant
orthologous variants: 134084752-G-C

26035599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: 3 prime UTR variant
orthologous variants: 134084752-G-T

26035621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: 3 prime UTR variant
orthologous variants: 134084734-G-T

26035711-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: 3 prime UTR variant
orthologous variants: 134084700-T-A

26035711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: 3 prime UTR variant
orthologous variants: 134084700-T-C

26035711-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: 3 prime UTR variant
orthologous variants: 134084700-T-G

http://identifiers.org/hco/1/GRCh38#26035743-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#134084651-A-C

26035743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: 3 prime UTR variant
orthologous variants: 134084651-A-G

26035743-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: 3 prime UTR variant
orthologous variants: 134084651-A-T

26035751-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: 3 prime UTR variant
orthologous variants: 134084643-G-C

26035751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: 3 prime UTR variant
orthologous variants: 134084643-G-T

26035779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: 3 prime UTR variant
orthologous variants: 134084619-G-A

26035882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: 3 prime UTR variant
orthologous variants: 134084532-A-G

http://identifiers.org/hco/1/GRCh38#26035898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#134084527-C-A

26035898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: 3 prime UTR variant
orthologous variants: 134084527-C-T

26035909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: 3 prime UTR variant
orthologous variants: 134084517-C-T

26035990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: 3 prime UTR variant
orthologous variants: 134084442-A-G

26036078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: 3 prime UTR variant
orthologous variants: 134084386-C-T

26036086-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: 3 prime UTR variant
orthologous variants: 134084379-C-G

26036086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: 3 prime UTR variant
orthologous variants: 134084379-C-T

26036124-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: 3 prime UTR variant
orthologous variants: 134084342-G-T

http://identifiers.org/hco/1/GRCh38#26036131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#134084335-C-A

26036217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 134083894-G-A

26036217-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 134083894-G-C

26036227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: 3 prime UTR variant
orthologous variants: 134083884-A-G

26036228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: 3 prime UTR variant
orthologous variants: 134083883-G-A

26036228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: 3 prime UTR variant
orthologous variants: 134083883-G-T

26036270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 134083848-T-C

26036309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: 3 prime UTR variant
orthologous variants: 134083825-T-C

26036314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: 3 prime UTR variant
orthologous variants: 134083820-T-C

26036319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: 3 prime UTR variant
orthologous variants: 134083815-G-A

26036319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: 3 prime UTR variant
orthologous variants: 134083815-G-T

26036336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: 3 prime UTR variant
orthologous variants: 134083796-C-T

26036429-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 134083701-C-G

26036429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3515
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 134083701-C-T