42555242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 82986083-C-T

42555266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 82986107-T-C

42555396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82986200-C-T

http://identifiers.org/hco/22/GRCh38#42555540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#82986370-C-A

42555540-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82986370-C-G

42555914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82986690-A-G

http://identifiers.org/hco/22/GRCh38#42555947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#82986706-C-A

42555947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82986706-C-T

http://identifiers.org/hco/22/GRCh38#42555962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#82986721-C-A

42555962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82986721-C-T

42556033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82986796-G-A

42556033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82986796-G-T

42556225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82986943-G-A

42556312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82987021-G-A

42556312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82987021-G-T

42556333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82987029-G-A

42556564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82987185-G-A

42556670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82987292-G-A

http://identifiers.org/hco/22/GRCh38#42556759-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#82987381-A-C

42556792-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82987414-G-C

42556792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82987414-G-T

42556943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82987565-G-A

42556966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82987588-A-G

42557612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82987979-G-A

42557888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82988193-C-T

42557974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82988267-G-A

http://identifiers.org/hco/22/GRCh38#42558139-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#82988381-A-C

42560132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82989756-T-C

http://identifiers.org/hco/22/GRCh38#42560160-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#82989784-C-A

42560160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82989784-C-T

http://identifiers.org/hco/22/GRCh38#42560181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#82989807-C-A

42560181-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 82989807-C-G

http://identifiers.org/hco/22/GRCh38#42560198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#82989824-C-A

42560198-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82989824-C-G

42560198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82989824-C-T

42560261-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82989887-C-G

42560261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82989887-C-T

42560346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82989944-G-A

42560346-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82989944-G-C

42560346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82989944-G-T

42560360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82989957-G-A

42560360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82989957-G-T

http://identifiers.org/hco/22/GRCh38#42560451-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#82990042-A-C

42560452-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82990043-C-G

42560452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82990043-C-T

42560454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82990045-C-T

42566117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82996229-G-A

http://identifiers.org/hco/22/GRCh38#42566229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#82996348-C-A

42566229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82996348-C-T

http://identifiers.org/hco/22/GRCh38#42566249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#82996364-C-A

42566249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82996364-C-T

42566278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82996386-T-C

42566290-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82996399-G-C

42570769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82998219-G-T

http://identifiers.org/hco/22/GRCh38#42570848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#82998284-C-A

42570848-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82998284-C-G

42570874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82998309-G-T

42570892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82998318-C-T

42571004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82998442-G-T

42571008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82998446-G-T

42571021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82998459-G-T

http://identifiers.org/hco/22/GRCh38#42571022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#82998460-C-A

42571022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82998460-C-T

42571023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82998461-C-T

42571062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82998491-G-A

42571062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82998491-G-T

42571072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82998501-G-A

42571087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82998517-G-A

42571087-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82998517-G-C

42571087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82998517-G-T

42571103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82998533-A-G

http://identifiers.org/hco/22/GRCh38#42571142-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#82998579-A-C

42571142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82998579-A-G

42571142-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82998579-A-T

42571159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82998596-T-C

42571257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82998683-G-A

42571257-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82998683-G-C

42571257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82998683-G-T

42571258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82998684-A-G

42571286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82998711-G-A

42571307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82998730-G-A

42571307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82998730-G-T

42571328-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82998750-G-C

42571328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82998750-G-T

42571378-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82998804-T-A

42571378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82998804-T-C

42571396-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82998825-C-G

42571396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82998825-C-T

http://identifiers.org/hco/22/GRCh38#42571446-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#82998872-A-C

42571446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82998872-A-G

42572125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82999484-T-C

42572141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82999500-T-C

42572170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82999519-C-T

42572365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82999708-G-T

42572394-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82999737-T-G

42572427-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82999759-A-T

42572463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82999795-A-G

42572503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82999838-G-A

42572503-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82999838-G-C

42572517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82999852-C-T

42572521-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82999856-C-G

42572521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82999856-C-T

42572631-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82999958-C-G

http://identifiers.org/hco/22/GRCh38#42572638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#82999965-C-A

42572638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82999965-C-T

42572664-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82999978-G-C

42572664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82999978-G-T

42572739-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83000048-T-A

http://identifiers.org/hco/22/GRCh38#42573920-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#83000445-C-A

42573920-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 83000445-C-G

42573920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 83000445-C-T

42574036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 83000561-T-C

42574036-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 83000561-T-G

http://identifiers.org/hco/22/GRCh38#42574050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#83000575-C-A

42574050-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 83000575-C-G

42574052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 83000577-G-A

42574052-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 83000577-G-C

42574089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 83000602-C-T

42574121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 83000631-G-A

42574150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 83000656-A-G

42574186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 83000703-G-A

42574186-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 83000703-G-C

http://identifiers.org/hco/22/GRCh38#42574244-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#83000751-A-C

42574244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 83000751-A-G

42574244-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 83000751-A-T

http://identifiers.org/hco/22/GRCh38#42574282-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#83000784-A-C

42574282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 83000784-A-G

42574341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 83000838-G-A

42574341-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 83000838-G-C

42574341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 83000838-G-T

42574376-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 83000866-A-T

http://identifiers.org/hco/22/GRCh38#42574440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83000918-C-A

42574440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83000918-C-T

42574455-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83000935-T-A

42574455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83000935-T-C

42574461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83000941-G-A

42574461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83000941-G-T

42574576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83001020-G-A

42574576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83001020-G-T

42574577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83001021-G-A

42574577-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83001021-G-C

42574577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83001021-G-T

http://identifiers.org/hco/22/GRCh38#42574599-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83001039-C-A

http://identifiers.org/hco/22/GRCh38#42574638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83001078-C-A

42574772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: non coding transcript exon variant
orthologous variants: 83001126-G-A

42574772-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: non coding transcript exon variant
orthologous variants: 83001126-G-C

42574772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: non coding transcript exon variant
orthologous variants: 83001126-G-T

42574827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83001181-G-A

http://identifiers.org/hco/22/GRCh38#42574856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83001204-C-A

42574856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83001204-C-T

http://identifiers.org/hco/22/GRCh38#42574932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83001246-C-A

42574932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83001246-C-T

42574962-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83001267-T-G

42574965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83001274-G-A

42575025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83001331-G-A

42575883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83001692-G-A

42575883-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83001692-G-C

42575883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83001692-G-T

42575901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83001719-G-A

42575901-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83001719-G-C

42575901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83001719-G-T

42575907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83001725-G-A

42575907-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83001725-G-C

42575907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83001725-G-T

42575923-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 83001742-T-A

42575923-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 83001742-T-G

42575959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: non coding transcript exon variant
orthologous variants: 83001778-G-A

42575959-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: non coding transcript exon variant
orthologous variants: 83001778-G-T

42575986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: non coding transcript exon variant
orthologous variants: 83001808-G-A

42575986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: non coding transcript exon variant
orthologous variants: 83001808-G-T

42576007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: non coding transcript exon variant
orthologous variants: 83001829-C-T

42576046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: non coding transcript exon variant
orthologous variants: 83001868-A-G

http://identifiers.org/hco/22/GRCh38#42576067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83001889-C-A

42576094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: non coding transcript exon variant
orthologous variants: 83001916-G-A

42576094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: non coding transcript exon variant
orthologous variants: 83001916-G-T

42576154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83001973-G-A

42576154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83001973-G-T

42576204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83002024-T-C

42576204-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83002024-T-G

http://identifiers.org/hco/22/GRCh38#42576247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83002059-C-A

42576247-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83002059-C-G

42576247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83002059-C-T

42576272-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83002071-T-G

http://identifiers.org/hco/22/GRCh38#42576435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83002208-C-A

42576435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83002208-C-T

http://identifiers.org/hco/22/GRCh38#42576476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83002250-C-A

42576476-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83002250-C-G

42576476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83002250-C-T

42576482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83002256-G-A

42576482-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83002256-G-C

42576482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83002256-G-T

http://identifiers.org/hco/22/GRCh38#42576500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83002266-C-A

42576500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83002266-C-T

42576536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: non coding transcript exon variant
orthologous variants: 83002302-C-T

42576547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: non coding transcript exon variant
orthologous variants: 83002313-T-C

42576653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83003073-G-A

42576653-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83003073-G-C

42576653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83003073-G-T

42576660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83003080-G-A

42576660-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83003080-G-C

42576660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83003080-G-T

42576707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83003125-G-T

42576708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83003126-G-A

42576708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83003126-G-T

http://identifiers.org/hco/22/GRCh38#42576709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83003127-C-A

42576709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83003127-C-T

42576748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83003191-G-A

42576748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83003191-G-T

42576804-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83003228-A-T

42576846-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83003260-C-G

42576846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83003260-C-T

42576852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83003266-C-T

http://identifiers.org/hco/22/GRCh38#42576887-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83003289-A-C

42576895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83003297-T-C

42576895-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83003297-T-G

http://identifiers.org/hco/22/GRCh38#42576935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83003340-C-A

42576948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83003353-A-G

http://identifiers.org/hco/22/GRCh38#42577391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83003712-C-A

42577391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83003712-C-T

42577465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83003781-G-A

42577572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83003876-G-A

http://identifiers.org/hco/22/GRCh38#42577637-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83003913-A-C

42577637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83003913-A-G

http://identifiers.org/hco/22/GRCh38#42577694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83003954-C-A

42577694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83003954-C-T

http://identifiers.org/hco/22/GRCh38#42577721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83003981-C-A

42577721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83003981-C-T

http://identifiers.org/hco/22/GRCh38#42577760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83004018-C-A

42577760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83004018-C-T

42577810-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83004056-T-A

42577810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83004056-T-C

http://identifiers.org/hco/22/GRCh38#42577813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83004059-C-A

42577813-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83004059-C-G

42577813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83004059-C-T

42577845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 83004094-G-A

42577845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 83004094-G-T

42577858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: non coding transcript exon variant
orthologous variants: 83004107-G-A

42577858-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: non coding transcript exon variant
orthologous variants: 83004107-G-C

42577858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: non coding transcript exon variant
orthologous variants: 83004107-G-T

42577986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83004245-G-A

42577986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83004245-G-T

http://identifiers.org/hco/22/GRCh38#42578010-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83004254-A-C

42578040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83004273-A-G

42578040-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83004273-A-T

42578041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83004274-G-A

42578041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83004274-G-T

http://identifiers.org/hco/22/GRCh38#42578106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83004325-C-A

42578106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83004325-C-T

http://identifiers.org/hco/22/GRCh38#42578109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83004328-C-A

42578109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83004328-C-T

42578125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83004351-T-C

42580103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83005939-G-A

42580114-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83005949-T-A

42580114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83005949-T-C

42580118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83005953-T-C

http://identifiers.org/hco/22/GRCh38#42580132-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83005967-C-A

42580132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83005967-C-T

42580349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: non coding transcript exon variant
orthologous variants: 83006165-G-T

42580367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 83006183-G-A

42580367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 83006183-G-T

42580403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83006218-G-A

42581749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 83006681-G-A

42581782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83006712-T-C

http://identifiers.org/hco/22/GRCh38#42581797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#83006747-C-A

42581797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 83006747-C-T

http://identifiers.org/hco/22/GRCh38#42581872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#83006814-C-A

42581872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 83006814-C-T

42581925-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 83006859-T-A

42581925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 83006859-T-C

http://identifiers.org/hco/22/GRCh38#42581979-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#83006913-A-C

42581979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: non coding transcript exon variant
orthologous variants: 83006913-A-G

42581979-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: non coding transcript exon variant
orthologous variants: 83006913-A-T

http://identifiers.org/hco/22/GRCh38#42582026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#83006961-C-A

42582026-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 83006961-C-G

42582026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30454
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 83006961-C-T