http://identifiers.org/hco/5/GRCh38#132311488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#53899331-C-A

132311488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53899331-C-T

132311529-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53899292-G-T

132311546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53899274-T-C

132311616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53899206-T-C

132311616-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53899206-T-G

132311774-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53899049-T-A

http://identifiers.org/hco/5/GRCh38#132311807-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#53899018-A-C

132311807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53899018-A-G

132311807-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53899018-A-T

132311808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53899017-G-A

132311808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53899017-G-T

132311817-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53899008-T-G

132311972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53898876-T-C

http://identifiers.org/hco/5/GRCh38#132312000-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#53898852-A-C

132312061-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53898791-G-C

132312061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53898791-G-T

132312294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53898563-A-G

132312294-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53898563-A-T

132312344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53898514-G-T

132312584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53898086-C-T

132312862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53897815-G-A

132312993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53897720-T-C

132313162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53897543-G-A

132313162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53897543-G-T

132313412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53896569-A-G

132313423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53896558-T-C

132313445-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53896536-A-T

132313486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53896502-G-A

132313486-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53896502-G-C

132313486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53896502-G-T

http://identifiers.org/hco/5/GRCh38#132313491-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#53896497-A-C

132313491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53896497-A-G

132313491-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53896497-A-T

132313536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53896433-T-C

132313723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 53896263-G-A

http://identifiers.org/hco/5/GRCh38#132313789-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#53896197-A-C

132313827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53896159-A-G

132313831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53896155-G-A

132313837-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53896149-A-T

132313889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53896086-G-A

132313889-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53896086-G-C

132314193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53895802-G-A

132314308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53895699-C-T

132314404-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53895598-T-A

132314420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53895581-G-A

http://identifiers.org/hco/5/GRCh38#132314445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#53895556-C-A

132314463-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53895546-A-T

132314627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53895387-T-C

132314834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53895197-C-T

132314957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53895071-G-A

132314990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53895034-G-A

http://identifiers.org/hco/5/GRCh38#132315707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#53893975-C-A

132315707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53893975-C-T

132315967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53893751-C-T

132316052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53893652-A-G

132316058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53893646-C-T

132316269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53893426-G-A

132316297-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53893399-G-C

132316348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53893363-C-T

132316415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53893312-A-G

132316482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53893249-T-C

132318519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53891683-G-A

132318570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53891635-G-A

132318686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53891576-G-A

http://identifiers.org/hco/5/GRCh38#132318994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#53891315-C-A

132318994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53891315-C-T

132319032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53891271-G-A

132320494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53889443-G-A

132320554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53889384-T-C

132320604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53889359-C-T

132320844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53889157-T-C

132320844-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53889157-T-G

132320922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53889067-T-C

http://identifiers.org/hco/5/GRCh38#132321008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#53888991-C-A

132321008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53888991-C-T

http://identifiers.org/hco/5/GRCh38#132321033-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#53888966-C-A

132321081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53888909-G-T

132321087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53888899-T-C

132321287-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53888774-A-T

http://identifiers.org/hco/5/GRCh38#132322216-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#53888340-A-C

132322288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 53888268-A-G

132322324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 53888232-G-A

132322324-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 53888232-G-C

132322375-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53888179-A-T

http://identifiers.org/hco/5/GRCh38#132322433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#53888124-C-A

132322440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53888118-T-C

132322441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53888117-G-A

132322441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53888117-G-T

132322447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53888111-G-A

132322447-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53888111-G-C

132322584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53888006-T-C

132322612-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53887969-C-G

132322612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53887969-C-T

132322634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53887947-G-A

132323217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53817167-A-G

132323410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53816990-G-A

132323419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53816987-G-A

132324316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53814178-G-A

132324316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53814178-G-T

132324741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53813813-A-G

132324913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53813683-G-A

132325112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53813531-T-C

132326825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53811978-G-A

http://identifiers.org/hco/5/GRCh38#132326877-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#53811930-A-C

132327043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53811599-G-A

132327044-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53811598-T-A

http://identifiers.org/hco/5/GRCh38#132327237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#53886954-C-A

132327237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53886954-C-T

132327258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53886933-T-C

132327258-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53886933-T-G

132327374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 53886817-G-A

132327389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53886802-T-C

132327389-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53886802-T-G

132327398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53886793-G-A

132327398-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53886793-G-C

132327422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53886762-T-C

132327431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53886753-A-G

132327466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53886716-A-G

132327534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53886660-A-G

132327750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53885962-A-G

132327885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53885824-A-G

132328138-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53885572-C-G

132328259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53885463-A-G

132328671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53884963-A-G

132329274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53884604-A-G

132329424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53884456-T-C

132329460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53884420-C-T

132329475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53884385-T-C

132329570-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53884293-C-G

132329659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53884206-T-C

132331828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53882831-A-G

132331835-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53882824-T-A

132331835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53882824-T-C

http://identifiers.org/hco/5/GRCh38#132331866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#53882793-C-A

132331866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53882793-C-T

132331874-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53882785-T-A

132331874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53882785-T-C

http://identifiers.org/hco/5/GRCh38#132331884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#53882775-C-A

132331884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53882775-C-T

132331896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53882763-A-G

http://identifiers.org/hco/5/GRCh38#132331899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#53882760-C-A

132331899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53882760-C-T

132331970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53882690-A-G

http://identifiers.org/hco/5/GRCh38#132332625-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#53882471-A-C

132332736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53882340-A-G

132333007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53882107-T-C

http://identifiers.org/hco/5/GRCh38#132334642-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#53881742-A-C

132334642-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53881742-A-T

132334941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53881439-T-C

132335484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53880092-G-A

http://identifiers.org/hco/5/GRCh38#132335643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#53879940-C-A

132335744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53879851-G-T

132335783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53879822-A-G

http://identifiers.org/hco/5/GRCh38#132335850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#53879756-C-A

132335850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53879756-C-T

132339583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53878421-A-G

http://identifiers.org/hco/5/GRCh38#132339683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#53878350-C-A

132339901-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53878170-T-G

132340037-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53878006-A-T

132340071-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53877971-T-G

132340233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53877734-C-T

132340324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53877649-C-T

132340379-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53877615-G-C

132340546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53877456-T-C

132340743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53877261-G-A

132342470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53875892-C-T

http://identifiers.org/hco/5/GRCh38#132342484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#53875877-C-A

132342484-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53875877-C-G

132342524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53875841-A-G

http://identifiers.org/hco/5/GRCh38#132342529-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#53875836-A-C

http://identifiers.org/hco/5/GRCh38#132342546-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#53875819-A-C

http://identifiers.org/hco/5/GRCh38#132342693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#53875701-C-A

132342816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53875597-T-C

132342845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53875568-A-G

132342907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53875529-G-A

132342969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53875449-C-T

http://identifiers.org/hco/5/GRCh38#132343063-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#53875365-A-C

132343301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53875127-T-C

132343504-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53874795-A-T

132343546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53874717-G-A

132343581-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53874683-T-G

132343612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53874649-A-G

132343712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53874557-G-A

132343741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53874528-G-A

http://identifiers.org/hco/5/GRCh38#132343768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#53874501-C-A

132343768-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53874501-C-G

132343788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53874481-T-C

http://identifiers.org/hco/5/GRCh38#132343805-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#53874464-A-C

132343962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53874175-A-G

http://identifiers.org/hco/5/GRCh38#132343967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#53874170-C-A

132343967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53874170-C-T

http://identifiers.org/hco/5/GRCh38#132343997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#53874140-C-A

132344282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53873819-A-G

132345332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53805997-T-C

132358198-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53802147-C-G

132358314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53802032-A-G

132358340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53801979-A-G

132358853-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53800125-T-A

132359474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53799649-G-A

132365923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53789221-A-G

132366146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53789006-T-C

132366233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53788940-T-C

132367956-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53785392-T-G

132368423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53785053-G-A

132368423-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53785053-G-C

http://identifiers.org/hco/5/GRCh38#132368577-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#53784895-A-C

132368602-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53784854-T-G

132368802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53784631-T-C

132369227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53871797-A-G

http://identifiers.org/hco/5/GRCh38#132369541-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#53871112-A-C

132369541-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53871112-A-T

http://identifiers.org/hco/5/GRCh38#132369554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#53871097-C-A

132369554-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53871097-C-G

132369554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53871097-C-T

http://identifiers.org/hco/5/GRCh38#132369567-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#53871084-A-C

132369567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53871084-A-G

132369580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53871070-G-A

132369580-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53871070-G-C

132369580-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53871070-G-T

132369592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53871058-G-A

132369592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53871058-G-T

http://identifiers.org/hco/5/GRCh38#132369598-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#53871052-A-C

132369598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53871052-A-G

132369598-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53871052-A-T

http://identifiers.org/hco/5/GRCh38#132369616-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#53871041-A-C

132369616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53871041-A-G

132369616-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53871041-A-T

http://identifiers.org/hco/5/GRCh38#132369648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#53782678-C-A

132369648-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53782678-C-G

132369648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53782678-C-T

http://identifiers.org/hco/5/GRCh38#132369649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#53782677-C-A

132369649-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53782677-C-G

132369649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53782677-C-T

http://identifiers.org/hco/5/GRCh38#132369712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#53782601-C-A

132369712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53782601-C-T

132369713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53782600-T-C

132369713-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53782600-T-G

132369714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53782599-T-C

132369714-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53782599-T-G

132369807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53782485-G-A

http://identifiers.org/hco/5/GRCh38#132369813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#53782479-C-A

132369852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 53782441-G-A

132369852-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 53782441-G-C

132369852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 53782441-G-T

132369896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 53782426-G-A

132369941-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 53782395-C-G

132369942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 53782394-A-G

132369942-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 53782394-A-T

132369968-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 53782368-G-C

132370003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 53782333-C-T

132370009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 53782327-G-A

132370009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 53782327-G-T

132370016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 53782320-G-A

132370016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 53782320-G-T

132370108-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 53782228-C-G

132370108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 53782228-C-T

132370129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40538
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 53782207-C-T