http://identifiers.org/hco/2/GRCh38#112138405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#128705861-C-A

112138405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 128705861-C-T

http://identifiers.org/hco/2/GRCh38#112138429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#128705885-C-A

112138429-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 128705885-C-G

112138429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 128705885-C-T

http://identifiers.org/hco/2/GRCh38#112138443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#128705899-C-A

112138443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 128705899-C-T

http://identifiers.org/hco/2/GRCh38#112138464-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#128705916-A-C

112138464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 128705916-A-G

http://identifiers.org/hco/2/GRCh38#112138486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128705921-C-A

112138486-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 128705921-C-G

112138490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 128705925-G-A

112138490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 128705925-G-T

http://identifiers.org/hco/2/GRCh38#112138549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128705938-C-A

112138549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 128705938-C-T

112138623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 128705960-C-T

112140445-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128706174-G-C

112140668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128706362-A-G

112140680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128706374-T-C

112140927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128706769-G-A

http://identifiers.org/hco/2/GRCh38#112140981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128706856-C-A

112141381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128707153-G-T

112141491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128707265-T-C

112141651-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128707417-G-C

112141737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128707498-A-G

112141785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128707523-C-T

112142216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128707890-C-T

112142574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128708361-G-A

112142649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128708454-C-T

112142768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128708578-T-C

112142768-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128708578-T-G

112142890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128708693-G-A

112150416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128712522-G-A

112150586-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128712656-T-G

http://identifiers.org/hco/2/GRCh38#112150635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#128712700-C-A

112150635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128712700-C-T

112150790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128712841-G-A

112152350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128712942-G-A

112152350-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128712942-G-C

112152350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128712942-G-T

http://identifiers.org/hco/2/GRCh38#112153395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128713876-C-A

112153805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128714264-G-A

112153843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128714288-C-T

112153879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128714324-C-T

112154541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128715479-G-A

112154554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128715492-G-T

112154654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128715562-G-A

112154776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128715673-T-C

112154988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128715864-A-G

112155409-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128716289-C-G

112155435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128716319-A-G

112155562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128716463-G-A

112155699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128716596-G-A

http://identifiers.org/hco/2/GRCh38#112155929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128716768-C-A

112155996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128716813-C-T

112156125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128716894-C-T

112156264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128717009-G-A

http://identifiers.org/hco/2/GRCh38#112156446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128717181-C-A

112156447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128717182-G-A

112156657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128717398-C-T

112156974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128717687-G-A

112159252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128718602-C-T

112159340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128718682-G-A

112159340-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128718682-G-C

112159416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128718751-C-T

112159462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128718795-C-T

112159546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128719005-T-C

112159546-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128719005-T-G

http://identifiers.org/hco/2/GRCh38#112159550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128719009-C-A

112159550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128719009-C-T

112159559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128719111-G-T

112159561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128719160-G-A

112159561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128719160-G-T

http://identifiers.org/hco/2/GRCh38#112159569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128719168-C-A

http://identifiers.org/hco/2/GRCh38#112159586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128719204-C-A

112159592-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128719210-C-G

112159626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128719243-G-T

http://identifiers.org/hco/2/GRCh38#112159673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128719277-C-A

http://identifiers.org/hco/2/GRCh38#112159704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/2/GRCm39#128719308-C-A

112159704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 128719308-C-T

http://identifiers.org/hco/2/GRCh38#112159711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128719315-C-A

112159711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 128719315-C-T

112159780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 128719384-C-T

112159851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128719457-G-A

112159851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128719457-G-T

http://identifiers.org/hco/2/GRCh38#112159879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128719480-C-A

112159879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128719480-C-T

http://identifiers.org/hco/2/GRCh38#112159892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128719493-C-A

112159892-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128719493-C-G

112159892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128719493-C-T

112159893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128719494-G-A

112159893-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128719494-G-C

112159893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128719494-G-T

http://identifiers.org/hco/2/GRCh38#112161100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128721382-C-A

112161100-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128721382-C-G

112164951-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128722127-G-C

112164973-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128722148-C-G

112164973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128722148-C-T

112165011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 128722186-G-A

112165012-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 128722187-G-C

112165075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 128722250-C-T

112165142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 128722317-C-T

112165564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128724130-T-C

112165648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128724193-C-T

112165746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128724288-A-G

112165774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128724307-G-A

112165854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128724384-C-T

112166036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128724551-G-A

112166549-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128724878-T-G

112166550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128724879-A-G

112166651-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128724969-G-C

112166782-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128725098-C-G

112166782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128725098-C-T

112168556-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128726413-C-G

112168763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128727397-G-T

112168933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128727552-A-G

http://identifiers.org/hco/2/GRCh38#112168968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128727583-C-A

112168968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128727583-C-T

112173682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128729443-G-A

112173726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128729507-A-G

112173904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128729691-G-A

112174619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128730349-G-A

112174623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128730353-A-G

112175050-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128730648-C-G

112175050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128730648-C-T

112175091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128730742-T-C

http://identifiers.org/hco/2/GRCh38#112175187-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128730834-A-C

112175311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128731071-G-A

112175311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128731071-G-T

112175376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128731187-C-T

112175575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128731369-G-T

112175588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128731406-G-A

112175588-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128731406-G-C

112175588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128731406-G-T

112175604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128731527-G-A

112175604-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128731527-G-C

http://identifiers.org/hco/2/GRCh38#112175636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128731556-C-A

112175636-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128731556-C-G

112175880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128731786-T-C

http://identifiers.org/hco/2/GRCh38#112175917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128731822-C-A

112175917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128731822-C-T

http://identifiers.org/hco/2/GRCh38#112175935-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128731840-A-C

112175954-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128731858-T-A

112175954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128731858-T-C

112175954-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128731858-T-G

112175977-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128731881-T-A

http://identifiers.org/hco/2/GRCh38#112175981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128731889-C-A

112175981-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128731889-C-G

112176032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128731936-A-G

http://identifiers.org/hco/2/GRCh38#112176039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128731943-C-A

112176039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128731943-C-T

112176084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128731972-T-C

112176087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128731975-C-T

http://identifiers.org/hco/2/GRCh38#112176146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128732031-C-A

http://identifiers.org/hco/2/GRCh38#112176166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128732051-C-A

112176178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128732063-G-A

112176178-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128732063-G-C

http://identifiers.org/hco/2/GRCh38#112176182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128732067-C-A

http://identifiers.org/hco/2/GRCh38#112176184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128732068-C-A

http://identifiers.org/hco/2/GRCh38#112176209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128732093-C-A

http://identifiers.org/hco/2/GRCh38#112176225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128732109-C-A

112176235-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128732114-T-A

112176235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128732114-T-C

112176235-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128732114-T-G

http://identifiers.org/hco/2/GRCh38#112176244-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128732116-A-C

112176259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128732131-T-C

112176365-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128732166-T-A

112176422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128732223-C-T

112176427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128732228-A-G

http://identifiers.org/hco/2/GRCh38#112176451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128732249-C-A

112176548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128732309-G-A

112176548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128732309-G-T

112176783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128732746-A-G

112176790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128732753-G-T

112177239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128732799-G-T

http://identifiers.org/hco/2/GRCh38#112181366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128734043-C-A

112181372-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128734049-A-T

112181563-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128734210-C-G

112181569-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128734216-G-C

http://identifiers.org/hco/2/GRCh38#112181613-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128734263-A-C

112181613-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128734263-A-T

112181624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128734274-A-G

112181656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128734298-G-T

http://identifiers.org/hco/2/GRCh38#112181692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#128734312-C-A

112181692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128734312-C-T

http://identifiers.org/hco/2/GRCh38#112181744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128734368-C-A

112181744-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 128734368-C-G

http://identifiers.org/hco/2/GRCh38#112181752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128734376-C-A

112181752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 128734376-C-T

http://identifiers.org/hco/2/GRCh38#112181755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128734379-C-A

112181755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 128734379-C-T

http://identifiers.org/hco/2/GRCh38#112181779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#128734403-C-A

112181779-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 128734403-C-G

112181779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 128734403-C-T

http://identifiers.org/hco/2/GRCh38#112181872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/2/GRCm39#128734499-C-A

112181872-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 128734499-C-G

112181872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 128734499-C-T

112181914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 128734519-G-A

112181914-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 128734519-G-C

112181914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 128734519-G-T

http://identifiers.org/hco/2/GRCh38#112181929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#128734534-C-A

112181929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 128734534-C-T

112181964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 128734596-G-A

112181964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 128734596-G-T

http://identifiers.org/hco/2/GRCh38#112181999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128734632-C-A

112181999-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 128734632-C-G

112181999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 128734632-C-T

112182000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 128734633-T-C

112182023-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128734654-G-C

http://identifiers.org/hco/2/GRCh38#112182677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128735608-C-A

112182689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128735620-G-A

112182689-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128735620-G-C

112182689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128735620-G-T

http://identifiers.org/hco/2/GRCh38#112182777-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128735673-A-C

112182933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128735855-G-A

112182933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128735855-G-T

112182972-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128735894-G-C

112182988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128735920-A-G

http://identifiers.org/hco/2/GRCh38#112183033-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128735965-C-A

http://identifiers.org/hco/2/GRCh38#112183061-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128735993-C-A

112183082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128736014-G-A

http://identifiers.org/hco/2/GRCh38#112183088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128736020-C-A

112183650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128736499-G-T

112183725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128736569-A-G

112185163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128736645-C-T

112185164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128736646-A-G

112185171-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128736653-T-G

112185180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128736665-G-T

112185185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128736670-A-G

112185185-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128736670-A-T

112185337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 128736822-A-G

112185422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128736912-A-G

112185919-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128736996-A-T

112187110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128737116-C-T

http://identifiers.org/hco/2/GRCh38#112187134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128737137-C-A

112187185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 128737188-G-T

112187269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 128737272-T-C

112187335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 128737338-C-T

112187371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 128737374-T-C

112187422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 128737425-C-T

112187431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 128737434-G-A

112187431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 128737434-G-T

http://identifiers.org/hco/2/GRCh38#112187568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128737576-C-A

112187568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 128737576-C-T

112187579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 128737587-G-A

http://identifiers.org/hco/2/GRCh38#112187605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#128737621-C-A

http://identifiers.org/hco/2/GRCh38#112187606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#128737622-C-A

112187606-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 128737622-C-G

112187606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 128737622-C-T

http://identifiers.org/hco/2/GRCh38#112187624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128737641-C-A

112187624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 128737641-C-T

112187638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128737655-G-T

http://identifiers.org/hco/2/GRCh38#112187652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128737669-C-A

112187652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128737669-C-T

http://identifiers.org/hco/2/GRCh38#112187719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128737744-C-A

112187719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128737744-C-T

112187733-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128737756-T-A

112187733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128737756-T-C

112187733-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128737756-T-G

112187741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128737764-G-A

112187741-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128737764-G-T

http://identifiers.org/hco/2/GRCh38#112187750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128737773-C-A

112187750-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128737773-C-G

http://identifiers.org/hco/2/GRCh38#112187776-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128737805-A-C

112187776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128737805-A-G

http://identifiers.org/hco/2/GRCh38#112187851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#128737883-C-A

112187851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128737883-C-T

112187857-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128737889-G-C

112187857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128737889-G-T

112187865-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128737899-T-A

112187865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128737899-T-C

112187866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128737900-G-T

112187869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128737903-T-C

112187875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128737909-C-T

http://identifiers.org/hco/2/GRCh38#112187877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128737911-C-A

112187877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128737911-C-T

112187890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128737924-G-A

112187890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128737924-G-T

http://identifiers.org/hco/2/GRCh38#112187899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128737933-C-A

112187899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128737933-C-T

112187906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128737940-T-C

112187930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128737963-G-A

112187930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128737963-G-T

http://identifiers.org/hco/2/GRCh38#112188049-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128738034-A-C

http://identifiers.org/hco/2/GRCh38#112188078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#128738064-C-A

112188084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128738070-A-G

112188203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128738184-A-G

112188203-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128738184-A-T

112188236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128738217-A-G

112188341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128738294-G-A

112188341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128738294-G-T

112188406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128738360-G-A

112188406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128738360-G-T

112188431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128738385-G-T

112188440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128738394-G-A

112188440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128738394-G-T

http://identifiers.org/hco/2/GRCh38#112188451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128738405-C-A

http://identifiers.org/hco/2/GRCh38#112188483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128738440-C-A

112188483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128738440-C-T

http://identifiers.org/hco/2/GRCh38#112188485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128738442-C-A

112188489-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128738446-C-G

112188616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128738547-A-G

112188616-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128738547-A-T

112188828-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128738857-C-G

112188867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128738894-A-G

http://identifiers.org/hco/2/GRCh38#112188912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128738949-C-A

112188912-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128738949-C-G

http://identifiers.org/hco/2/GRCh38#112188913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128738950-C-A

112189271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128739277-C-T

http://identifiers.org/hco/2/GRCh38#112189302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128739308-C-A

112189325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128739327-G-A

112189362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26740
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128739364-C-T