101965545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121487326-C-T

http://identifiers.org/hco/15/GRCh38#101965666-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121487422-C-A

101965845-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121487539-C-G

101965845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121487539-C-T

http://identifiers.org/hco/15/GRCh38#101965893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121487578-C-A

101965893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121487578-C-T

101965908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121487593-G-A

101965908-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121487593-G-C

101965908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121487593-G-T

http://identifiers.org/hco/15/GRCh38#101965910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121487595-C-A

101965910-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121487595-C-G

101965910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121487595-C-T

http://identifiers.org/hco/15/GRCh38#101965933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121487615-C-A

101965933-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121487615-C-G

101965933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121487615-C-T

101965993-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121487668-C-G

101965993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121487668-C-T

101966050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121487695-G-A

101966050-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121487695-G-C

101966050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121487695-G-T

101966057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121487702-C-T

101966099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: non coding transcript exon variant
orthologous variants: 121487744-T-C

101966141-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: non coding transcript exon variant
orthologous variants: 121487784-G-C

101966141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: non coding transcript exon variant
orthologous variants: 121487784-G-T

101966146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: non coding transcript exon variant
orthologous variants: 121487789-G-A

101966146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: non coding transcript exon variant
orthologous variants: 121487789-G-T

101966163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 121487806-T-C

http://identifiers.org/hco/15/GRCh38#101966169-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#121487812-A-C

101966169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 121487812-A-G

http://identifiers.org/hco/15/GRCh38#101966175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#121487817-C-A

101966175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 121487817-C-T

http://identifiers.org/hco/15/GRCh38#101966183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121487825-C-A

101966183-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: non coding transcript exon variant
orthologous variants: 121487825-C-G

101966183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: non coding transcript exon variant
orthologous variants: 121487825-C-T

http://identifiers.org/hco/15/GRCh38#101966205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121487844-C-A

101966205-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: non coding transcript exon variant
orthologous variants: 121487844-C-G

101966205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: non coding transcript exon variant
orthologous variants: 121487844-C-T

101966284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121487931-G-A

101966284-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121487931-G-C

101966284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121487931-G-T

http://identifiers.org/hco/15/GRCh38#101966326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121487966-C-A

101966326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121487966-C-T

101966343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121487982-G-T

http://identifiers.org/hco/15/GRCh38#101966436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121488079-C-A

101966436-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121488079-C-G

101966436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121488079-C-T

http://identifiers.org/hco/15/GRCh38#101966457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121488098-C-A

101966457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121488098-C-T

101966479-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121488126-T-G

101966527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121488160-A-G

http://identifiers.org/hco/15/GRCh38#101966528-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121488161-A-C

http://identifiers.org/hco/15/GRCh38#101966529-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121488162-A-C

101966529-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121488162-A-T

http://identifiers.org/hco/15/GRCh38#101966579-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121488206-A-C

http://identifiers.org/hco/15/GRCh38#101966582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121488209-C-A

101966582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121488209-C-T

101967296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121489712-G-A

101967423-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121489840-C-G

101967423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121489840-C-T

101967486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121489916-C-T

http://identifiers.org/hco/15/GRCh38#101967551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121490386-C-A

101967551-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121490386-C-G

101967551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121490386-C-T

101967623-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121490448-C-G

101967623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121490448-C-T

101967749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121490555-G-T

101967765-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121490571-A-T

101967769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121490575-T-C

101967794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121490600-A-G

101967799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121490605-A-G

101967802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121490608-G-A

101967966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121490771-A-G

101968087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121490881-T-C

101968138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121490936-C-T

101969319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121491062-T-C

http://identifiers.org/hco/15/GRCh38#101969340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121491079-C-A

101969340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121491079-C-T

101969345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121491084-G-A

101969345-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121491084-G-C

101969362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121491109-C-T

101969481-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121491217-T-A

101969501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121491237-G-T

101969641-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121491342-G-C

101970261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121495079-G-A

101970266-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121495084-A-T

101970359-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121495181-C-G

101970359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121495181-C-T

101970596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121495388-T-C

101970616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121495406-G-A

101970616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121495406-G-T

101970685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121495491-T-C

http://identifiers.org/hco/15/GRCh38#101970688-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121495494-A-C

101970688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121495494-A-G

101970746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121495535-G-A

101970749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121495538-T-C

101970757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121495546-G-T

http://identifiers.org/hco/15/GRCh38#101970770-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121495559-A-C

101970770-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121495559-A-T

101970777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121495564-T-C

101970783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121495570-A-G

http://identifiers.org/hco/15/GRCh38#101970828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#121495615-C-A

http://identifiers.org/hco/15/GRCh38#101970831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#121495618-C-A

101970831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121495618-C-T

http://identifiers.org/hco/15/GRCh38#101970878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121495661-C-A

101970878-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121495661-C-G

101971163-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121495888-T-G

101971406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121496086-G-A

101971407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121496087-C-T

101971647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121496244-G-A

101971673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121496260-G-T

101971713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121496299-G-A

101971921-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121496685-G-C

101971950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121496713-C-T

101971986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121496750-A-G

http://identifiers.org/hco/15/GRCh38#101972021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121496785-C-A

101972084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121496844-G-T

101972121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121496873-A-G

101972230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121496956-G-A

101972230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121496956-G-T

101972237-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121496963-T-G

101972281-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121497013-T-G

101972371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121497119-C-T

101972386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121497140-C-T

http://identifiers.org/hco/15/GRCh38#101972394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121497148-C-A

101972394-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121497148-C-G

101972414-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121497168-T-G

101972431-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121497185-C-G

101972431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121497185-C-T

101972451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121497205-G-A

101972451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121497205-G-T

101972467-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 121497221-T-G

101972480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121497231-A-G

101972480-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121497231-A-T

101972497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121497248-G-A

101972497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121497248-G-T

101972525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121497278-G-A

101972525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121497278-G-T

101972545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121497303-G-A

101972596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 121497357-G-A

101972596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 121497357-G-T

101972628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: non coding transcript exon variant
orthologous variants: 121497389-T-C

101972714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121497425-G-A

101972714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121497425-G-T

http://identifiers.org/hco/15/GRCh38#101972739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121497448-C-A

http://identifiers.org/hco/15/GRCh38#101972814-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121497493-A-C

101972814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121497493-A-G

101972818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121497497-T-C

101972833-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121497505-C-G

101972841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121497513-A-G

http://identifiers.org/hco/15/GRCh38#101972878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121497547-C-A

101972878-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121497547-C-G

101972878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121497547-C-T

101972911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: non coding transcript exon variant
orthologous variants: 121497579-G-A

101972911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: non coding transcript exon variant
orthologous variants: 121497579-G-T

http://identifiers.org/hco/15/GRCh38#101973008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121497663-C-A

http://identifiers.org/hco/15/GRCh38#101973088-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121497736-A-C

101973091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121497740-G-A

http://identifiers.org/hco/15/GRCh38#101973195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121497838-C-A

http://identifiers.org/hco/15/GRCh38#101973215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121497854-C-A

http://identifiers.org/hco/15/GRCh38#101973235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121497874-C-A

101973235-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: non coding transcript exon variant
orthologous variants: 121497874-C-G

101973235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: non coding transcript exon variant
orthologous variants: 121497874-C-T

101973282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: non coding transcript exon variant
orthologous variants: 121497952-G-A

101973292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: non coding transcript exon variant
orthologous variants: 121497959-G-A

101973292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: non coding transcript exon variant
orthologous variants: 121497959-G-T

101973321-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: non coding transcript exon variant
orthologous variants: 121497988-T-A

101973378-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121498054-G-C

101973378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121498054-G-T

101973396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121498072-G-A

101973396-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121498072-G-C

101973412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121498088-G-A

101973538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121498199-A-G

http://identifiers.org/hco/15/GRCh38#101973563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121498220-C-A

101973563-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121498220-C-G

101973563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121498220-C-T

101973759-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121498381-T-A

101973759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121498381-T-C

101973759-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121498381-T-G

101973760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121498382-G-A

101973760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121498382-G-T

http://identifiers.org/hco/15/GRCh38#101973779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121498396-C-A

101973779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121498396-C-T

101973949-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: non coding transcript exon variant
orthologous variants: 121498555-T-A

101973949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: non coding transcript exon variant
orthologous variants: 121498555-T-C

101973949-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: non coding transcript exon variant
orthologous variants: 121498555-T-G

http://identifiers.org/hco/15/GRCh38#101973967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121498562-C-A

101973967-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: non coding transcript exon variant
orthologous variants: 121498562-C-G

101973967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: non coding transcript exon variant
orthologous variants: 121498562-C-T

http://identifiers.org/hco/15/GRCh38#101974076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121498636-C-A

101974076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: non coding transcript exon variant
orthologous variants: 121498636-C-T

http://identifiers.org/hco/15/GRCh38#101974136-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121498687-C-A

http://identifiers.org/hco/15/GRCh38#101974137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121498688-C-A

101974137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121498688-C-T

101974206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: non coding transcript exon variant
orthologous variants: 121498752-G-A

101974206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: non coding transcript exon variant
orthologous variants: 121498752-G-T

http://identifiers.org/hco/15/GRCh38#101974223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121498768-C-A

101974223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: non coding transcript exon variant
orthologous variants: 121498768-C-T

101974310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: non coding transcript exon variant
orthologous variants: 121498849-A-G

101974383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121498891-T-C

101974392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121498900-G-A

101974474-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121498976-T-G

101974564-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121499066-T-A

101974610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121499112-G-A

101974639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121499141-T-C

101974723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121499211-G-A

101974798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121499305-G-A

101974917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121499374-A-G

101974933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121499388-G-A

101974933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121499388-G-T

101974940-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121499395-G-C

101974940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121499395-G-T

101974950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121499413-G-A

101974950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121499413-G-T

http://identifiers.org/hco/15/GRCh38#101974951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121499414-C-A

101974964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121499427-G-T

101975001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121499470-T-C

http://identifiers.org/hco/15/GRCh38#101975022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#121499491-C-A

101975022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: non coding transcript exon variant
orthologous variants: 121499491-C-T

101975035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: non coding transcript exon variant
orthologous variants: 121499504-G-A

101975035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: non coding transcript exon variant
orthologous variants: 121499504-G-T

101975055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: non coding transcript exon variant
orthologous variants: 121499524-G-A

101975055-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: non coding transcript exon variant
orthologous variants: 121499524-G-C

101975055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24362
most severe consequence: non coding transcript exon variant
orthologous variants: 121499524-G-T