http://identifiers.org/hco/15/GRCh38#98437288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68012725-C-A

98437288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: non coding transcript exon variant
orthologous variants: 68012725-C-T

98437299-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: non coding transcript exon variant
orthologous variants: 68012714-T-A

98437378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: non coding transcript exon variant
orthologous variants: 68012643-C-T

98437466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: non coding transcript exon variant
orthologous variants: 68012568-A-G

98437467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: non coding transcript exon variant
orthologous variants: 68012567-T-C

98437467-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: non coding transcript exon variant
orthologous variants: 68012567-T-G

http://identifiers.org/hco/15/GRCh38#98437472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68012562-C-A

98437490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: non coding transcript exon variant
orthologous variants: 68012544-G-T

98437583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: non coding transcript exon variant
orthologous variants: 68012457-T-C

98437595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: non coding transcript exon variant
orthologous variants: 68012445-T-C

http://identifiers.org/hco/15/GRCh38#98437598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68012442-C-A

98437598-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: non coding transcript exon variant
orthologous variants: 68012442-C-G

http://identifiers.org/hco/15/GRCh38#98437615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68012425-C-A

98437615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: non coding transcript exon variant
orthologous variants: 68012425-C-T

http://identifiers.org/hco/15/GRCh38#98437623-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68012417-A-C

98437729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: non coding transcript exon variant
orthologous variants: 68012319-A-G

98437731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: non coding transcript exon variant
orthologous variants: 68012317-G-A

98437737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: non coding transcript exon variant
orthologous variants: 68012311-A-G

98437746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: non coding transcript exon variant
orthologous variants: 68012303-G-T

98437749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: non coding transcript exon variant
orthologous variants: 68012300-T-C

98437749-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: non coding transcript exon variant
orthologous variants: 68012300-T-G

98440295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68008733-A-G

98440305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68008723-G-T

98440317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68008711-G-T

98440382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68008650-G-T

98440383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68008649-A-G

98440392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68008640-C-T

98440462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68008585-C-T

98440617-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68008472-C-G

98440617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68008472-C-T

98440771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68008328-C-T

98440926-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68008179-G-C

98440926-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68008179-G-T

98441127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: non coding transcript exon variant
orthologous variants: 68007978-C-T

98441165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 68007937-G-A

98442223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68007743-A-G

98442443-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68007518-G-C

98442574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 68007394-G-A

98442638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68007321-G-T

98442668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68007291-C-T

http://identifiers.org/hco/15/GRCh38#98443017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68006936-C-A

98443564-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68006156-T-A

98443594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68006126-A-G

http://identifiers.org/hco/15/GRCh38#98443650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68006088-C-A

98443650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68006088-C-T

98443779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68005976-G-A

http://identifiers.org/hco/15/GRCh38#98443908-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68005879-A-C

http://identifiers.org/hco/15/GRCh38#98444151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68005674-C-A

98444243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68005581-T-C

98444326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68005529-G-A

98444499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68005372-C-T

http://identifiers.org/hco/15/GRCh38#98444695-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68005174-A-C

98444721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68005144-C-T

98445748-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68003744-T-A

98445798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68003701-G-A

98445798-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68003701-G-C

98445855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68003654-T-C

http://identifiers.org/hco/15/GRCh38#98445859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68003649-C-A

98445899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68003603-G-T

98445903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68003599-T-C

98445903-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68003599-T-G

98445932-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68003570-T-A

98445932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68003570-T-C

98445932-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68003570-T-G

98445984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68003504-T-C

98446062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68003421-C-T

98446113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68003370-A-G

98446116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68003367-A-G

http://identifiers.org/hco/15/GRCh38#98446155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68003328-C-A

98446155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68003328-C-T

http://identifiers.org/hco/15/GRCh38#98446165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68003320-C-A

98446171-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68003314-T-A

98446171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68003314-T-C

98446210-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68003280-A-T

98446229-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68003262-T-A

98446229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68003262-T-C

98446257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68003232-G-A

98446257-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68003232-G-C

98446257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68003232-G-T

http://identifiers.org/hco/15/GRCh38#98446267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68003225-C-A

98446267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68003225-C-T

98447372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68001940-G-A

98447379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68001933-A-G

98447406-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68001905-T-A

98447406-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68001905-T-G

98447543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68001755-C-T

http://identifiers.org/hco/15/GRCh38#98451590-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68000371-A-C

98451590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68000371-A-G

98451710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68000279-A-G

98451736-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68000254-C-G

98451736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68000254-C-T

http://identifiers.org/hco/15/GRCh38#98451760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68000231-C-A

98451760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68000231-C-T

98451776-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68000216-T-A

98451781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68000211-T-C

http://identifiers.org/hco/15/GRCh38#98451970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#68000020-C-A

98451970-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: non coding transcript exon variant
orthologous variants: 68000020-C-G

98451970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: non coding transcript exon variant
orthologous variants: 68000020-C-T

98451986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: non coding transcript exon variant
orthologous variants: 68000004-C-T

http://identifiers.org/hco/15/GRCh38#98466929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#67990257-C-A

98466929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67990257-C-T

98466972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67990216-T-C

http://identifiers.org/hco/15/GRCh38#98467069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#67990129-C-A

98467085-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67990117-G-C

98467186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67990044-G-T

http://identifiers.org/hco/15/GRCh38#98467199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#67990031-C-A

98467222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67990008-T-C

98467397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67989860-T-C

98472895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67989458-G-A

98473561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67988821-A-G

98473589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67988793-C-T

98473723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67988623-G-A

98473723-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67988623-G-C

98473768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67988581-T-C

98473769-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67988580-G-C

98473875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67988477-G-A

98479777-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67979686-T-G

98479986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67979561-G-A

98480442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67979287-C-T

98480451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67979278-G-T

98480521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67979221-G-A

98480767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: non coding transcript exon variant
orthologous variants: 67978978-A-G

98480868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67978911-A-G

http://identifiers.org/hco/15/GRCh38#98480871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#67978908-C-A

98480871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67978908-C-T

98480872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67978907-A-G

98480886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67978893-G-T

98481078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67978753-T-C

98482714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67976002-C-T

98483026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67975721-G-A

http://identifiers.org/hco/15/GRCh38#98483053-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#67975697-A-C

98483391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67975380-A-G

98484759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67973165-A-G

98484759-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67973165-A-T

98484903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67973031-C-T

98484908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67973026-A-G

98485104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67972864-A-G

98485124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67972843-A-G

98485599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67972371-A-G

http://identifiers.org/hco/15/GRCh38#98485743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#67972243-C-A

98485743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67972243-C-T

http://identifiers.org/hco/15/GRCh38#98486023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#67971519-C-A

98486023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67971519-C-T

98486026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67971516-A-G

98486026-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67971516-A-T

http://identifiers.org/hco/15/GRCh38#98486027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#67971515-C-A

98486027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67971515-C-T

98486093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67971458-G-A

98486093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67971458-G-T

98486234-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67971226-G-C

98486617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67970219-C-T

http://identifiers.org/hco/15/GRCh38#98486657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#67970174-C-A

98486657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67970174-C-T

98486879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67969962-C-T

98486964-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67969889-G-C

98487045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67969812-A-G

98487416-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67969594-T-G

98487437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67969573-G-A

98487512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67969494-G-A

98488146-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67969418-T-A

http://identifiers.org/hco/15/GRCh38#98488151-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#67969413-A-C

98488312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67969181-G-A

98488390-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67969111-G-C

98488424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67969079-A-G

98490279-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67968667-T-A

98490490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67968469-G-A

98490682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67968293-A-G

98490736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67968212-C-T

98490841-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67968076-T-A

98490841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67968076-T-C

98490936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67967981-C-T

98491028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67967894-G-A

98491212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67967715-G-A

98491311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67967622-G-A

98491733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67967249-T-C

98491748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67967234-C-T

98491889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67967126-C-T

http://identifiers.org/hco/15/GRCh38#98491917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#67967086-C-A

98491917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67967086-C-T

98503074-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67963856-T-A

98503074-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67963856-T-G

98503613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67963556-G-A

98503901-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67963260-G-C

http://identifiers.org/hco/15/GRCh38#98504057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#67963082-C-A

98504057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67963082-C-T

98504180-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67962955-T-G

98504363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67962755-G-A

98504526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67962604-T-C

98505093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67962101-G-A

98505101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67962093-T-C

98505581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67961716-T-C

98505581-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67961716-T-G

98505618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67961679-G-A

98505799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67961436-T-C

98505820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67961415-C-T

98506119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67961095-T-C

http://identifiers.org/hco/15/GRCh38#98506155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#67961062-C-A

98506345-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67960876-A-T

98506623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67960622-A-G

98506664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67960581-C-T

98506768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67960456-G-T

98507079-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67960138-T-G

98507831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67959840-C-T

98512552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67958484-G-A

98512552-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67958484-G-C

98512574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67958462-C-T

http://identifiers.org/hco/15/GRCh38#98512693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#67957984-C-A

98512694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67957983-C-T

http://identifiers.org/hco/15/GRCh38#98512850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#67957854-C-A

98513039-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67957669-G-C

98513482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67957552-C-T

98513794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67957281-G-A

98513808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67957268-A-G

98513820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67957256-A-G

98513820-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67957256-A-T

98513837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67957239-C-T

98513842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 67957235-C-T

98514186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67956946-A-G

http://identifiers.org/hco/15/GRCh38#98514214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#67956919-C-A

98514276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67956855-A-G

98514815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67956151-C-T

98514821-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67956145-C-G

98516514-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67953819-G-C

98516672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67953681-G-T

98516756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67953601-G-T

98517825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67953244-T-C

98518982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67952770-T-C

98518993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67952762-A-G

http://identifiers.org/hco/15/GRCh38#98519016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#67952739-C-A

http://identifiers.org/hco/15/GRCh38#98519028-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#67952727-C-A

98519028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67952727-C-T

98519283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67952503-G-A

98519359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67952435-G-A

98519359-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67952435-G-C

98519411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67952376-C-T

98519418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67952369-T-C

98519465-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67952341-C-G

http://identifiers.org/hco/15/GRCh38#98520237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#67950728-C-A

http://identifiers.org/hco/15/GRCh38#98520333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#67950632-C-A

http://identifiers.org/hco/15/GRCh38#98520351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#67950614-C-A

98520351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26835
most severe consequence: non coding transcript exon variant
orthologous variants: 67950614-C-T