195959749-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: non coding transcript exon variant
orthologous variants: 74469851-T-A

195959749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: non coding transcript exon variant
orthologous variants: 74469851-T-C

195959899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: non coding transcript exon variant
orthologous variants: 74470011-A-G

195959899-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: non coding transcript exon variant
orthologous variants: 74470011-A-T

195960005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: non coding transcript exon variant
orthologous variants: 74470111-T-C

http://identifiers.org/hco/3/GRCh38#195960007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74470113-C-A

195960008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: non coding transcript exon variant
orthologous variants: 74470114-A-G

195960015-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: non coding transcript exon variant
orthologous variants: 74470121-C-G

195960015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: non coding transcript exon variant
orthologous variants: 74470121-C-T

195963178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74471037-G-A

195963178-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74471037-G-C

195963178-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74471037-G-T

195963181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74471040-A-G

195963183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74471042-G-A

195963183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74471042-G-T

195963198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74471074-G-A

195963198-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74471074-G-C

195963198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74471074-G-T

http://identifiers.org/hco/3/GRCh38#195963236-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74471113-A-C

195963236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74471113-A-G

195963236-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74471113-A-T

195963250-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74471127-T-A

195963250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74471127-T-C

http://identifiers.org/hco/3/GRCh38#195963288-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74471164-A-C

195963288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74471164-A-G

195963288-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74471164-A-T

195963344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: non coding transcript exon variant
orthologous variants: 74471215-G-T

195965183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74471734-T-C

195965249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74471801-T-C

195965293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74471841-G-A

195965459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: non coding transcript exon variant
orthologous variants: 74471990-G-A

195965486-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: non coding transcript exon variant
orthologous variants: 74472017-G-C

195965486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: non coding transcript exon variant
orthologous variants: 74472017-G-T

195965635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74472142-G-A

195965635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74472142-G-T

http://identifiers.org/hco/3/GRCh38#195965666-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74472154-C-A

195965666-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74472154-C-G

195965666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74472154-C-T

http://identifiers.org/hco/3/GRCh38#195965701-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74472173-A-C

195967404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74474951-T-C

195967404-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74474951-T-G

195967425-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74474971-T-A

http://identifiers.org/hco/3/GRCh38#195967427-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74474973-A-C

http://identifiers.org/hco/3/GRCh38#195967454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74475001-C-A

195967454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74475001-C-T

http://identifiers.org/hco/3/GRCh38#195967478-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74475012-A-C

http://identifiers.org/hco/3/GRCh38#195967489-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74475023-A-C

195967489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74475023-A-G

195967495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74475028-G-A

195967504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74475037-G-A

195967504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74475037-G-T

195967510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74475042-G-A

195967510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74475042-G-T

http://identifiers.org/hco/3/GRCh38#195967535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74475067-C-A

195967535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: non coding transcript exon variant
orthologous variants: 74475067-C-T

195967544-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: non coding transcript exon variant
orthologous variants: 74475076-T-G

http://identifiers.org/hco/3/GRCh38#195967586-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74475118-A-C

195967589-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: non coding transcript exon variant
orthologous variants: 74475121-T-A

195967589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: non coding transcript exon variant
orthologous variants: 74475121-T-C

195967589-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: non coding transcript exon variant
orthologous variants: 74475121-T-G

195967791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74475287-A-G

195967859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74475346-A-G

195967886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: non coding transcript exon variant
orthologous variants: 74475373-A-G

http://identifiers.org/hco/3/GRCh38#195968017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74475501-C-A

195968017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74475501-C-T

195968195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74475653-T-C

http://identifiers.org/hco/3/GRCh38#195971341-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74476434-C-A

195971341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: non coding transcript exon variant
orthologous variants: 74476434-C-T

195971392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: non coding transcript exon variant
orthologous variants: 74476482-A-G

195971392-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: non coding transcript exon variant
orthologous variants: 74476482-A-T

195971404-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: non coding transcript exon variant
orthologous variants: 74476494-T-A

195971404-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: non coding transcript exon variant
orthologous variants: 74476494-T-G

195971430-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: non coding transcript exon variant
orthologous variants: 74476520-G-C

195971430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: non coding transcript exon variant
orthologous variants: 74476520-G-T

195971434-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: non coding transcript exon variant
orthologous variants: 74476524-G-C

195971434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: non coding transcript exon variant
orthologous variants: 74476524-G-T

195971472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74476553-T-C

195971472-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74476553-T-G

195971484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74476568-A-G

195971484-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74476568-A-T

195971509-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74476597-T-A

195971511-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74476599-T-G

195971531-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74476618-T-A

195971531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74476618-T-C

195971579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74476666-A-G

195971621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74476704-G-A

195972035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74476757-A-G

195972086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74476806-G-A

195974356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74479375-G-T

195974498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: non coding transcript exon variant
orthologous variants: 74479521-A-G

195974525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: non coding transcript exon variant
orthologous variants: 74479548-G-A

195974525-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: non coding transcript exon variant
orthologous variants: 74479548-G-C

195974534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: non coding transcript exon variant
orthologous variants: 74479557-A-G

195974555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: non coding transcript exon variant
orthologous variants: 74479578-G-A

http://identifiers.org/hco/3/GRCh38#195974599-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74479618-A-C

195974599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74479618-A-G

http://identifiers.org/hco/3/GRCh38#195974606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74479625-C-A

http://identifiers.org/hco/3/GRCh38#195974610-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74479629-C-A

195974617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74479636-A-G

http://identifiers.org/hco/3/GRCh38#195974632-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74479650-A-C

195974632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74479650-A-G

195975057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74479727-T-C

195975060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74479730-C-T

195975328-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74479934-C-G

195975347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74479952-C-T

195975438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74479994-A-G

195975484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74480030-G-A

195975608-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74480160-T-A

195975608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74480160-T-C

195975626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74480178-A-G

195975626-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74480178-A-T

195975627-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74480179-T-G

195975635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74480187-G-A

195975635-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74480187-G-C

195975635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74480187-G-T

http://identifiers.org/hco/3/GRCh38#195975644-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74480196-A-C

195975644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74480196-A-G

195975644-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74480196-A-T

195975759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: non coding transcript exon variant
orthologous variants: 74480272-G-A

195975759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: non coding transcript exon variant
orthologous variants: 74480272-G-T

195975765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: non coding transcript exon variant
orthologous variants: 74480278-G-A

195975765-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: non coding transcript exon variant
orthologous variants: 74480278-G-C

195975765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: non coding transcript exon variant
orthologous variants: 74480278-G-T

195975807-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: non coding transcript exon variant
orthologous variants: 74480320-T-A

195975810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: non coding transcript exon variant
orthologous variants: 74480323-C-T

http://identifiers.org/hco/3/GRCh38#195975825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74480338-C-A

195975825-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: non coding transcript exon variant
orthologous variants: 74480338-C-G

http://identifiers.org/hco/3/GRCh38#195975923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74480426-C-A

195975923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74480426-C-T

http://identifiers.org/hco/3/GRCh38#195975953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74480452-C-A

195975953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74480452-C-T

195976001-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74480487-T-A

195976001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74480487-T-C

195976037-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74480524-C-G

195976037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74480524-C-T

http://identifiers.org/hco/3/GRCh38#195976684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74480755-C-A

http://identifiers.org/hco/3/GRCh38#195976934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74480967-C-A

195976934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74480967-C-T

http://identifiers.org/hco/3/GRCh38#195976941-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74480974-A-C

195976941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74480974-A-G

195976944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74480977-G-A

195976944-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74480977-G-C

195976944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74480977-G-T

195976968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74481000-G-A

195976968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74481000-G-T

http://identifiers.org/hco/3/GRCh38#195977020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74481069-C-A

195977020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74481069-C-T

http://identifiers.org/hco/3/GRCh38#195977041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74481092-C-A

195977041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74481092-C-T

195977060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74481120-T-C

195977065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74481125-G-A

195977065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74481125-G-T

195977154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: non coding transcript exon variant
orthologous variants: 74481212-G-A

195977154-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: non coding transcript exon variant
orthologous variants: 74481212-G-C

195977154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: non coding transcript exon variant
orthologous variants: 74481212-G-T

195977273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74481338-T-C

195977515-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74481537-C-G

195977531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74481553-G-A

195977532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74481554-C-T

195977592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74481603-G-A

195977601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74481611-G-A

195977741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74481721-C-T

195977904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74481830-A-G

195977919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74481845-A-G

195977937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74481862-G-A

195977970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74481885-T-C

195978001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74481915-A-G

195978001-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74481915-A-T

195978005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74481919-T-C

195978155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74482041-C-T

195978171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74482058-G-A

195978171-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74482058-G-C

195978171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74482058-G-T

195978198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74482080-C-T

http://identifiers.org/hco/3/GRCh38#195979686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74482362-C-A

195979693-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74482369-C-G

195979693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74482369-C-T

195979811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: non coding transcript exon variant
orthologous variants: 74482484-G-A

195979811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: non coding transcript exon variant
orthologous variants: 74482484-G-T

195979949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74482601-G-A

195979949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74482601-G-T

http://identifiers.org/hco/3/GRCh38#195980011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74482673-C-A

195980011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74482673-C-T

195980013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74482675-A-G

195980018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74482680-C-T

195980019-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74482681-A-T

195980112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74482760-T-C

195980112-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74482760-T-G

195981447-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74484895-T-G

195981475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74484921-C-T

195981489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74484935-T-C

http://identifiers.org/hco/3/GRCh38#195981552-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74484981-A-C

195981552-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74484981-A-T

195981586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74485005-T-C

195981760-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74485166-T-A

195981842-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74485232-T-G

195981895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74485282-T-C

195982011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74485362-G-T

http://identifiers.org/hco/3/GRCh38#195982030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74485381-C-A

195982030-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74485381-C-G

195982030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74485381-C-T

195982031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74485382-T-C

195982048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74485399-G-A

195982048-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74485399-G-C

195982048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74485399-G-T

195982053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74485404-G-A

195982053-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74485404-G-C

195982053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74485404-G-T

195982055-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74485406-G-C

195982069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74485420-T-C

http://identifiers.org/hco/3/GRCh38#195982109-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74485454-A-C

195982109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74485454-A-G

195982109-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74485454-A-T

195982118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74485471-T-C

195982118-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74485471-T-G

195982146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74485496-G-T

195982791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74485750-G-A

195982791-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74485750-G-C

195982810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74485769-C-T

http://identifiers.org/hco/3/GRCh38#195982815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74485775-C-A

195982815-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74485775-C-G

195982873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74485835-G-A

195982873-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74485835-G-C

195982874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74485836-C-T

195982893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74485855-T-C

195982895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74485857-G-A

195983019-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74485964-C-G

195983845-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74486569-C-G

195983940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74486656-C-T

http://identifiers.org/hco/3/GRCh38#195983978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74486694-C-A

195983978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74486694-C-T

195984124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: non coding transcript exon variant
orthologous variants: 74487178-G-A

195984124-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: non coding transcript exon variant
orthologous variants: 74487178-G-C

195984124-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: non coding transcript exon variant
orthologous variants: 74487178-G-T

http://identifiers.org/hco/3/GRCh38#195984265-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74487319-A-C

195984265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: non coding transcript exon variant
orthologous variants: 74487319-A-G

195984266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: non coding transcript exon variant
orthologous variants: 74487320-T-C

195984285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74487339-G-A

195984285-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74487339-G-C

195984285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74487339-G-T

http://identifiers.org/hco/3/GRCh38#195984384-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74487454-A-C

http://identifiers.org/hco/3/GRCh38#195984414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74487483-C-A

195984485-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 74487585-T-A

195984502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74487602-G-A

195984502-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74487602-G-C

195984502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74487602-G-T

http://identifiers.org/hco/3/GRCh38#195984579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74487676-C-A

195984579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74487676-C-T

195984745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 74487842-C-T

http://identifiers.org/hco/3/GRCh38#195984761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74487859-C-A

195984761-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74487859-C-G

195984761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74487859-C-T

195984786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74487869-T-C

195984786-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74487869-T-G

http://identifiers.org/hco/3/GRCh38#195984825-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74487908-A-C

195984825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74487908-A-G

195984856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74487939-G-A

195984856-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74487939-G-C

195984856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74487939-G-T

195984927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74487991-C-T

195985085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74488129-G-A

195985085-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74488129-G-C

195985085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74488129-G-T

http://identifiers.org/hco/3/GRCh38#195985397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74491256-C-A

195985397-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74491256-C-G

http://identifiers.org/hco/3/GRCh38#195985429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74491272-C-A

195985575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74491412-G-A

195985575-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74491412-G-C

195985575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74491412-G-T

195985600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74491431-G-A

195985600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74491431-G-T

195985657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: non coding transcript exon variant
orthologous variants: 74491486-A-G

http://identifiers.org/hco/3/GRCh38#195985815-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74491641-A-C

195985815-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74491641-A-T

195985925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74491745-C-T

http://identifiers.org/hco/3/GRCh38#195986036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74492331-C-A

195986036-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74492331-C-G

195986044-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74492339-C-G

http://identifiers.org/hco/3/GRCh38#195986118-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74492433-A-C

http://identifiers.org/hco/3/GRCh38#195986121-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74492436-A-C

195986233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74492546-C-T

195986342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74492655-G-A

195986342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74492655-G-T

195986409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74492710-A-G

195986409-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74492710-A-T

195986417-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74492721-T-A

195986486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74492943-T-C

195986595-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: non coding transcript exon variant
orthologous variants: 74493047-C-G

195986595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: non coding transcript exon variant
orthologous variants: 74493047-C-T

http://identifiers.org/hco/3/GRCh38#195986653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74493092-C-A

195986653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74493092-C-T

195986657-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74493096-T-A

195986657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74493096-T-C

195986661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74493100-G-A

195986661-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74493100-G-T

195986678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74493113-A-G

195986678-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74493113-A-T

195986682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74493117-T-C

195986685-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74493120-C-G

195986685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74493120-C-T

http://identifiers.org/hco/3/GRCh38#195986722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74493157-C-A

195986722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74493157-C-T

195986728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74493163-T-C

195986728-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74493163-T-G

195986805-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74493213-C-G

http://identifiers.org/hco/3/GRCh38#195986844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74493259-C-A

195986844-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74493259-C-G

195986871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74493284-A-G

195987043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74493417-T-C

195987043-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74493417-T-G

195987245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74493658-T-C

http://identifiers.org/hco/3/GRCh38#195987348-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74493695-A-C

195987348-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74493695-A-T

195987351-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74493698-T-A

195987351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74493698-T-C

195988989-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74497472-T-G

http://identifiers.org/hco/3/GRCh38#195989193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74497668-C-A

195989384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74497849-T-C

195989862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74498103-G-A

195989862-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74498103-G-C

195989869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74498110-G-A

195989871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74498112-G-A

195989899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74498121-C-T

195989901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74498123-G-A

195989901-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74498123-G-C

195989952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 74498145-G-A

195990057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74498186-G-A

195990057-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74498186-G-C

195990057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74498186-G-T

http://identifiers.org/hco/3/GRCh38#195990066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74498195-C-A

195990066-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74498195-C-G

195990066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74498195-C-T

195990083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74498212-G-A

195990083-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74498212-G-C

195990083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74498212-G-T

http://identifiers.org/hco/3/GRCh38#195990133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74498230-C-A

195990133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74498230-C-T

http://identifiers.org/hco/3/GRCh38#195990140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#74498237-C-A

195990140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 74498237-C-T

http://identifiers.org/hco/3/GRCh38#195990313-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#74498369-C-A

195990313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32455
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 74498369-C-T