94154200-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117979403-G-C

94154200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117979403-G-T

94154207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117979410-A-G

94154307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117979506-A-G

94154310-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117979509-T-G

94154342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117979541-G-A

94154383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117979586-G-T

94154390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117979593-G-A

94154390-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117979593-G-C

94154390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117979593-G-T

94154441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117979647-G-T

94154459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117979665-G-T

94154479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117979682-A-G

94154550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117979743-G-A

94154550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117979743-G-T

http://identifiers.org/hco/13/GRCh38#94154551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#117979744-C-A

94154551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117979744-C-T

94154556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117979749-G-A

94154556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117979749-G-T

94154577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117979763-G-A

http://identifiers.org/hco/13/GRCh38#94157002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#117982547-C-A

94157002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117982547-C-T

94157013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117982561-G-A

94157110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117982617-C-T

94157127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117982636-G-A

94157145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117982653-T-C

94157195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117982703-A-G

94157195-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117982703-A-T

94157299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117982769-T-C

94157339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117983308-G-A

94157382-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117983351-C-G

94157382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117983351-C-T

http://identifiers.org/hco/13/GRCh38#94157420-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#117983390-A-C

94157799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117983709-C-T

94157816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117983726-A-G

94157927-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117983827-T-G

http://identifiers.org/hco/13/GRCh38#94158054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#117983930-C-A

http://identifiers.org/hco/13/GRCh38#94158422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#117984278-C-A

94158583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117984438-A-G

94159783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117985278-A-G

94159854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117985343-T-C

94159948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117985438-A-G

94161014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117985897-C-T

94161020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117985900-C-T

94161045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117985925-C-T

94161363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117986622-C-T

94161376-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117986635-A-T

94161481-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117986733-A-T

94161504-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117986756-C-G

94161600-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117986836-G-C

http://identifiers.org/hco/13/GRCh38#94161657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#117986891-C-A

94161669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117986903-G-A

94161761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117986987-A-G

94162375-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117987412-G-C

94162386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117987423-C-T

94162388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117987425-T-C

94162424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117987460-G-A

94162478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117987538-G-A

94162508-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117987557-T-G

94162550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117987600-A-G

94162597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117987645-G-A

94162597-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117987645-G-C

94162701-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117987747-G-C

94163081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117988064-T-C

94163126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117988095-A-G

94163231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117988197-G-A

94163602-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117989202-A-T

94163708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117989312-G-T

94163895-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117989437-T-A

94163927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117989469-T-C

94164082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117989607-A-G

94164273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117989782-A-G

94164300-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117989808-T-G

http://identifiers.org/hco/13/GRCh38#94164518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#117990019-C-A

94164609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117990095-C-T

94165658-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117990438-A-T

94165881-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117990646-G-C

94165919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117990684-A-G

http://identifiers.org/hco/13/GRCh38#94166174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#117990935-C-A

94166257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117991018-G-A

94166627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117991382-G-A

94166661-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117991416-A-T

94166747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117991502-T-C

94166805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117991559-C-T

94167090-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117991845-A-T

94167108-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117991862-C-G

94167108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117991862-C-T

94167239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117991995-C-T

94168810-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117992547-T-G

http://identifiers.org/hco/13/GRCh38#94168911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#117992648-C-A

94169056-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117992772-A-T

94169122-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117992847-T-G

http://identifiers.org/hco/13/GRCh38#94169330-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#117993026-A-C

94169446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117993141-G-A

94169511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117993195-G-T

94169654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117993345-C-T

94169746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117993398-G-A

94169877-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117993529-A-T

94169932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117993582-G-A

94170051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117993707-G-T

94170319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117993967-A-G

94170328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117993976-G-A

94170481-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117994127-C-G

94170481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117994127-C-T

94170661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117994294-T-C

94170762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117994407-G-A

94170878-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117994476-C-G

94170898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117994496-G-A

94171069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117994667-G-A

94171069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117994667-G-T

94171274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117994817-C-T

94171305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117994847-T-C

94171485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117995032-C-T

94171597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117995144-G-T

94171787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117995344-C-T

94171844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117995388-A-G

94171932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117995473-G-A

94172098-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117995856-C-G

94172098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117995856-C-T

94172178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117995949-C-T

94172268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117996018-A-G

94172289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117996039-G-A

http://identifiers.org/hco/13/GRCh38#94172313-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#117996063-A-C

94172313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117996063-A-G

94172395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117996133-A-G

94172707-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117996433-T-G

94172884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117996610-C-T

94172924-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117996642-A-T

94172972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117996681-G-A

94172976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117996685-G-A

94173041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117996747-A-G

94173041-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117996747-A-T

94173084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117996801-C-T

94173642-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117997897-A-T

94173648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117997903-G-A

94173648-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117997903-G-C

94173653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117997908-C-T

94173687-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117997942-T-A

94173702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117997957-T-C

94173804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117998075-A-G

94173884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117998156-A-G

94174521-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117998780-A-T

94174638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117998893-A-G

94174772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117999030-A-G

94174993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117999249-T-C

94175032-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117999286-T-G

94175044-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117999298-T-A

94176113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117999880-G-A

94176221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117999986-G-A

94176230-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117999995-C-G

94176260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118000016-G-A

94176271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118000027-G-A

94176428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118000199-G-A

94176506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118000264-A-G

94176586-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118000344-T-A

94176601-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118000359-C-G

94176633-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118000394-C-G

94176652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118000413-C-T

94176832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118000593-C-T

94176858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118000619-C-T

94176915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118000666-G-A

94177047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118000785-A-G

94177132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118000880-G-T

94177355-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118001124-A-T

94177493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118001229-G-A

94177586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118001311-A-G

94177929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118001564-A-G

94178582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118001852-C-T

94178672-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118001943-C-G

94178760-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118002027-A-T

94179195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118002660-G-A

94179442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118002928-G-A

94179718-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118003224-A-T

94179857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118003347-A-G

94179899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118003389-A-G

94179899-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118003389-A-T

94180046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118003545-C-T

94180092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118003590-A-G

94180164-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118003687-G-C

94180192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118003728-C-T

94180206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118003742-C-T

94180218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118003753-A-G

94180262-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118003795-G-C

94180270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118003803-A-G

94180741-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118004248-G-C

94181306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118004623-C-T

94181436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118004661-G-A

94181487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118004713-G-T

http://identifiers.org/hco/13/GRCh38#94181843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118005010-C-A

94181864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118005031-T-C

94182203-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118005337-T-A

94182329-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118005459-T-A

94182430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118005558-A-G

94182431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118005559-T-C

94185917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118006864-G-A

94185917-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118006864-G-C

94185970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118006916-G-A

94185970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118006916-G-T

94186039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118006974-G-A

94186039-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118006974-G-T

94186124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118007019-G-A

94186832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118009014-A-G

http://identifiers.org/hco/13/GRCh38#94186864-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118009041-A-C

94186980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118009336-G-A

94186989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118009345-G-T

94187054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118009412-A-G

94187067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118009425-A-G

94187114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118009472-G-T

94187352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118009915-C-T

http://identifiers.org/hco/13/GRCh38#94187451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118010036-C-A

94187451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118010036-C-T

94187550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118010150-A-G

94187552-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118010152-C-G

94187552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118010152-C-T

http://identifiers.org/hco/13/GRCh38#94187737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118010620-C-A

94187774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118010653-A-G

94187862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118010867-G-A

http://identifiers.org/hco/13/GRCh38#94187920-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118010928-C-A

94187920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39909
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118010928-C-T