19242312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 145043180-C-T

19242492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 145043371-T-C

19243424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145046408-G-A

19243733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145046707-G-A

19243733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145046707-G-T

http://identifiers.org/hco/20/GRCh38#19243740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#145046714-C-A

19243740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145046714-C-T

19243805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145046778-A-G

http://identifiers.org/hco/20/GRCh38#19243845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#145046806-C-A

19243845-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145046806-C-G

19243886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 145046846-G-T

19243888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 145046848-T-C

19243888-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 145046848-T-G

19243963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 145046890-T-C

http://identifiers.org/hco/20/GRCh38#19244161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#145047073-C-A

19244161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 145047073-C-T

19244217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 145047133-C-T

19244354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145047252-A-G

19246308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145053257-T-C

19246357-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145053296-T-A

19246438-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145053376-T-A

19246622-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145053541-G-C

http://identifiers.org/hco/20/GRCh38#19246762-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#145053678-A-C

19246762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145053678-A-G

19246865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145053744-G-T

19246909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145053787-A-G

19246960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145053835-G-A

19247308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145054143-C-T

19247318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145054153-G-A

19247328-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145054163-T-G

http://identifiers.org/hco/20/GRCh38#19247595-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#145054446-A-C

19247640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145054480-T-C

19248180-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145054987-C-G

http://identifiers.org/hco/20/GRCh38#19249502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#145055541-C-A

19249502-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145055541-C-G

http://identifiers.org/hco/20/GRCh38#19249532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#145055571-C-A

19249812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145055852-C-T

19249837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145055869-A-G

19249959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145055976-G-A

19250982-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145057002-C-G

19251123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145057140-G-A

19251407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145057464-G-A

19251407-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145057464-G-C

19251802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145058341-A-G

19251898-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145058430-T-G

19252000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145058531-G-T

19252170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145058702-G-A

19252321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145058855-A-G

19252601-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145059144-C-G

19252601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145059144-C-T

19252830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145059372-G-A

19252904-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145059441-G-C

19253003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145059545-T-C

19253704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145060278-G-A

19254285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145061062-A-G

19254365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145061163-G-A

19254596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145061356-C-T

19254657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145061402-A-G

19254981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145061737-A-G

19255234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145061986-A-G

19257010-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145063364-C-G

19257126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145063481-T-C

19257137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145063520-G-A

19257271-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145063621-G-C

19257427-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145063744-C-G

19257479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145063790-G-A

19257479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145063790-G-T

19257495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145063806-A-G

19257525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145063829-C-T

19257568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145063868-G-A

19257568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145063868-G-T

19257582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145063882-T-C

19257600-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145063900-T-A

19257605-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145063906-A-T

19258732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145065373-G-T

19258733-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145065374-C-G

19258814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145065456-C-T

19259120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145065748-C-T

19259279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145065882-A-G

19259338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145065934-C-T

19259343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145065939-G-A

19259465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145066022-A-G

19259552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145066100-A-G

19259689-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145066212-C-G

19259699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145066222-G-A

19259788-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145066293-C-G

19259803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145066308-C-T

19259837-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145066347-C-G

19260364-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145066801-T-A

http://identifiers.org/hco/20/GRCh38#19260467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#145066883-C-A

19260489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145066902-G-A

19260659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145067074-C-T

19260712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145067126-G-T

19260777-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145067187-G-C

19261294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145067561-A-G

19261648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145067645-C-T

19261667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145067664-A-G

http://identifiers.org/hco/20/GRCh38#19262021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#145067981-C-A

19262054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145068014-C-T

19262063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145068023-T-C

19262696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145068291-G-T

19262826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145068356-C-T

19263410-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145068825-G-C

19263424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145068839-G-A

19263772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145069136-A-G

19263785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145069149-T-C

19263887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145069242-A-G

19263903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145069258-G-A

19264210-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145069343-C-G

19264267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145069401-G-A

19264267-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145069401-G-C

19264267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145069401-G-T

19264307-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145069441-C-G

19264307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145069441-C-T

http://identifiers.org/hco/20/GRCh38#19264387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#145069510-C-A

19264387-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145069510-C-G

19264435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145069562-G-A

19264876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145069710-T-C

19264876-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145069710-T-G

19264886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145069720-G-T

19264989-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145069817-C-G

19265091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145069970-A-G

19265467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145070277-G-A

http://identifiers.org/hco/20/GRCh38#19265712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#145070510-C-A

19265712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145070510-C-T

19265857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 145070662-G-A

19265857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 145070662-G-T

http://identifiers.org/hco/20/GRCh38#19265859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#145070664-C-A

19265859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 145070664-C-T

19265938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 145071057-G-A

http://identifiers.org/hco/20/GRCh38#19265955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#145071086-C-A

19265955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 145071086-C-T

http://identifiers.org/hco/20/GRCh38#19265997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#145071127-C-A

19265998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 145071128-T-C

http://identifiers.org/hco/20/GRCh38#19266000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#145071137-C-A

19266052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145071189-G-A

19266052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145071189-G-T

19266144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145071280-G-T

19266159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145071295-A-G

19266370-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145071501-G-C

19266486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145071616-C-T

19266602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145071736-G-A

19266714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145071864-G-A

19266721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145071871-T-C

http://identifiers.org/hco/20/GRCh38#19266742-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#145071891-A-C

19266742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145071891-A-G

19266790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145071951-C-T

19267369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145072405-G-T

19267460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145072474-A-G

19267944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145072879-C-T

19271110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145073257-G-A

19273245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145073550-G-A

19273554-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145073829-C-G

19273560-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145073830-G-C

19273608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145073874-G-A

19273626-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145073893-G-C

19273676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145073937-A-G

19274094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145074050-G-A

19274199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145074151-C-T

19274411-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145074347-T-A

19274411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145074347-T-C

19274414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145074350-A-G

19274551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145074420-A-G

19274559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145074428-A-G

19274741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145074761-A-G

19275013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145075025-G-A

19275044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145075054-A-G

19275192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145075186-A-G

19275230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145075225-A-G

19275246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145075233-T-C

19275533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145075696-A-G

http://identifiers.org/hco/20/GRCh38#19275669-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#145075848-A-C

19275677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145075864-A-G

19275686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145075873-G-A

19275749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145075937-C-T

19276110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145076307-G-A

19276216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145076414-A-G

19276284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145076470-G-T

19276311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145076497-G-A

19276311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145076497-G-T

19277199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145076744-G-A

19277445-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145076969-G-C

19277643-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145077152-T-G

19278041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145077556-G-T

19278915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145084898-A-G

19279018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145084996-T-C

19279217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145085179-G-A

19279307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145085399-G-A

19279417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145085537-G-A

19279417-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145085537-G-T

19279465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145085585-C-T

19279467-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145085587-G-C

19279851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145077591-G-T

19279924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145077522-C-T

19280043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145077393-C-T

19280396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145086241-T-C

19280521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145086365-A-G

19280685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145086525-G-A

19280685-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145086525-G-C

19280818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145086735-T-C

http://identifiers.org/hco/20/GRCh38#19280823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#145086740-C-A

19280823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145086740-C-T

19280827-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145086744-T-G

http://identifiers.org/hco/20/GRCh38#19280850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#145086770-C-A

19280850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145086770-C-T

19280894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145086814-G-T

19281061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 145086983-G-A

19281150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145087072-G-A

19281207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145087129-G-A

19281207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145087129-G-T

19283028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145088129-G-A

http://identifiers.org/hco/20/GRCh38#19283035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#145088136-C-A

19283044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145088145-G-T

19283157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 145088347-G-A

19283157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 145088347-G-T

19283378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145088554-A-G

19283491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145088904-G-A

19283710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145089148-T-C

19284316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 145090038-A-G

http://identifiers.org/hco/20/GRCh38#19284343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#145090066-C-A

19284346-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 145090069-T-G

19284528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40540
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 145090244-G-T