159194372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 173171610-T-C

159194375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 173171607-G-T

159194381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 173171601-G-A

159194381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 173171601-G-T

http://identifiers.org/hco/1/GRCh38#159194424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173171552-C-A

159194459-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 173171517-T-A

http://identifiers.org/hco/1/GRCh38#159194461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173171515-C-A

159194461-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 173171515-C-G

159194484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 173171480-C-T

159194506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 173171458-G-A

159194524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 173171443-C-T

159194585-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 173171382-T-A

159194585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 173171382-T-C

159194585-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 173171382-T-G

159194614-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 173171353-G-C

159194628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 173171340-A-G

159194672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 173171293-G-T

159194760-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 173171201-A-T

http://identifiers.org/hco/1/GRCh38#159194792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173171167-C-A

159194908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 173171049-A-G

159195001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 173170962-A-G

159195027-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 173170892-A-T

159195080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 173170842-T-C

http://identifiers.org/hco/1/GRCh38#159195106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173170816-C-A

159195106-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 173170816-C-G

http://identifiers.org/hco/1/GRCh38#159195254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173170669-C-A

159195254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 173170669-C-T

159195270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 173170653-G-A

159195270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 173170653-G-T

159195408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 173170522-G-T

159195538-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 173170396-A-T

159195614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 173170320-T-C

159195693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 173170241-G-A

159195693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 173170241-G-T

159195908-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 173170022-C-G

159195947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 173169983-G-T

159196099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 173169831-T-C

159196126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 173169809-A-G

159196199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 173169732-A-G

http://identifiers.org/hco/1/GRCh38#159196321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173169367-C-A

159196405-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 173169283-C-G

159196405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 173169283-C-T

159196548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 173169140-T-C

159196576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 173169112-T-C

159196586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 173169102-T-C

159196586-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 173169102-T-G

159196622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 173169069-A-G

159196622-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 173169069-A-T

159196643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 173169048-T-C

159196660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 173169029-T-C

159196665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 173169024-A-G

159196665-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 173169024-A-T

http://identifiers.org/hco/1/GRCh38#159196713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173168977-C-A

159196713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 173168977-C-T

159196717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 173168973-G-T

http://identifiers.org/hco/1/GRCh38#159196737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173168957-C-A

159196749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 173168945-C-T

159196866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 173168813-T-C

159196958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 173168721-C-T

http://identifiers.org/hco/1/GRCh38#159197048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#173168631-C-A

159197048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 173168631-C-T

159197154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 173168539-G-A

159197154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 173168539-G-T

159197175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 173168513-G-A

http://identifiers.org/hco/1/GRCh38#159197189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173168498-C-A

159197189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 173168498-C-T

http://identifiers.org/hco/1/GRCh38#159197221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173168475-C-A

159197388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 173168339-G-T

http://identifiers.org/hco/1/GRCh38#159197412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173168326-C-A

159197440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 173168310-C-T

159197456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 173168294-T-C

159197466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 173168284-G-A

159197466-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 173168284-G-C

159197466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 173168284-G-T

http://identifiers.org/hco/1/GRCh38#159197470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173168280-C-A

159197470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 173168280-C-T

http://identifiers.org/hco/1/GRCh38#159197478-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173168272-A-C

159197478-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 173168272-A-T

159197549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 173168202-G-T

159197579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 173168168-A-G

159197873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 173167693-G-A

http://identifiers.org/hco/1/GRCh38#159197884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173167681-C-A

http://identifiers.org/hco/1/GRCh38#159198003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173167559-C-A

159198161-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 173167284-A-T

159198593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173166944-A-G

http://identifiers.org/hco/1/GRCh38#159198680-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173166858-A-C

159198680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173166858-A-G

159198684-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173166854-G-C

159198978-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173166588-C-G

159199583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173165888-A-G

159200110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173165368-A-G

159200143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173165339-C-T

159200465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173165083-G-A

159200473-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173165075-G-C

159200476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173165072-G-A

159200509-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173165011-T-A

159200512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173165008-G-A

http://identifiers.org/hco/1/GRCh38#159200516-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173165004-A-C

159200520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173165000-A-G

159200522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173164998-A-G

159200635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173164867-A-G

159200963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 173164546-G-A

159200963-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 173164546-G-C

159200963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 173164546-G-T

http://identifiers.org/hco/1/GRCh38#159201096-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#173164413-A-C

159201096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 173164413-A-G

159201096-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 173164413-A-T

http://identifiers.org/hco/1/GRCh38#159201230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#173164278-C-A

159201230-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 173164278-C-G

159201230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 173164278-C-T

159201292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 173164235-A-G

http://identifiers.org/hco/1/GRCh38#159201326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#173164199-C-A

159201326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 173164199-C-T

159201452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 173164092-G-T

159201537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 173164016-G-T

http://identifiers.org/hco/1/GRCh38#159201620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#173163947-C-A

159201620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: 173163947-C-T

http://identifiers.org/hco/1/GRCh38#159201894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#173163669-C-A

159201936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 173163628-A-G

159202080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 173163477-T-C

159202092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 173163465-T-C

159202174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 173163360-G-T

159202179-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 173163355-T-A

159202179-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 173163355-T-G

159202221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 173163313-G-A

159202221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 173163313-G-T

http://identifiers.org/hco/1/GRCh38#159202289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#173163245-C-A

159202324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 173163214-G-T

http://identifiers.org/hco/1/GRCh38#159202338-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#173163201-C-A

159202340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 173163199-G-A

159202414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 173163124-G-A

159202414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 173163124-G-T

http://identifiers.org/hco/1/GRCh38#159202468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#173163077-C-A

159202521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 173163046-G-A

159202524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 173163043-G-T

http://identifiers.org/hco/1/GRCh38#159202534-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#173163033-C-A

http://identifiers.org/hco/1/GRCh38#159202660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#173162910-C-A

159202660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 173162910-C-T

159202673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 173162897-C-T

159202815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 173162756-G-A

159202815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 173162756-G-T

159202980-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 173162584-G-C

http://identifiers.org/hco/1/GRCh38#159203024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#173162540-C-A

159203024-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 173162540-C-G

159203028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 173162536-G-T

http://identifiers.org/hco/1/GRCh38#159203062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#173162498-C-A

159203062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 173162498-C-T

159203173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 173162387-T-C

159203238-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 173162331-T-A

159203238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 173162331-T-C

159203414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173162173-A-G

159203446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173162141-A-G

159203458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173162129-A-G

159203459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173162128-G-T

159203487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173162089-T-C

http://identifiers.org/hco/1/GRCh38#159203499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173162077-C-A

159203499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173162077-C-T

http://identifiers.org/hco/1/GRCh38#159203985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173161922-C-A

159204011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173161896-G-A

159204011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173161896-G-T

159204121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173161787-T-C

159204181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 173161727-G-T

159204200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173161708-T-C

159204242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 173161665-C-T

159204264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173161643-T-C

159204264-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173161643-T-G

159204368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 173161514-C-T

159204394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 173161493-G-A

159204394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 173161493-G-T

159204404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 173161483-A-G

http://identifiers.org/hco/1/GRCh38#159204519-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173161356-A-C

159204519-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173161356-A-T

http://identifiers.org/hco/1/GRCh38#159204532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173161343-C-A

159204532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173161343-C-T

http://identifiers.org/hco/1/GRCh38#159204536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173161339-C-A

http://identifiers.org/hco/1/GRCh38#159204539-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#173161336-A-C

159204539-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 173161336-A-T

159204714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173161255-C-T

159204740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173161225-A-G

http://identifiers.org/hco/1/GRCh38#159204786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173161180-C-A

159204786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173161180-C-T

http://identifiers.org/hco/1/GRCh38#159204810-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173161156-A-C

159204811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173161155-G-A

159204819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173161147-G-A

159204819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173161147-G-T

159204825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173161141-G-A

159204891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 173161042-T-C

159205082-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173160859-T-A

159205082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173160859-T-C

http://identifiers.org/hco/1/GRCh38#159205090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173160851-C-A

159205090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173160851-C-T

159205106-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173160835-T-A

159205106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173160835-T-C

159205122-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173160819-T-A

http://identifiers.org/hco/1/GRCh38#159205151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173160798-C-A

159205151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173160798-C-T

159205168-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173160781-T-A

159205168-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173160781-T-G

159205191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173160758-G-A

159205191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173160758-G-T

http://identifiers.org/hco/1/GRCh38#159205252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173160697-C-A

159205252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173160697-C-T

159205253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173160694-T-C

159205282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173160674-T-C

http://identifiers.org/hco/1/GRCh38#159205284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173160672-C-A

159205284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173160672-C-T

159205324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173160631-G-A

159205324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173160631-G-T

159205345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173160610-G-A

159205345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173160610-G-T

159205351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173160600-T-C

159205370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173160581-T-C

http://identifiers.org/hco/1/GRCh38#159205374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173160577-C-A

159205374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173160577-C-T

159205377-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173160574-T-A

159205377-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173160574-T-G

http://identifiers.org/hco/1/GRCh38#159205383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173160568-C-A

159205383-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173160568-C-G

159205383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173160568-C-T

159205440-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 173160515-T-G

http://identifiers.org/hco/1/GRCh38#159205454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#173160501-C-A

159205466-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 173160489-G-C

159205625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 173160336-G-T

159205669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 173160292-G-A

159205669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 173160292-G-T

159205809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 173160152-C-T

159205976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 173159985-A-G

159206006-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 173159955-T-A

159206063-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 173159898-C-G

159206064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 173159897-A-G

http://identifiers.org/hco/1/GRCh38#159206105-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#173159856-A-C

159206105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 173159856-A-G

159206211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 173159750-G-A

159206211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 173159750-G-T

159206246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 173159715-G-A

159206265-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 173159696-T-A

159206265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 173159696-T-C

http://identifiers.org/hco/1/GRCh38#159206564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173159379-C-A

159206564-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173159379-C-G

159206564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173159379-C-T

159206587-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173159362-T-A

159206587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173159362-T-C

159206611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173159339-G-A

159206612-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173159338-T-A

159206671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173159279-G-A

159206690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173159260-G-T

159206720-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173159233-T-A

159206818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173159125-G-A

159207212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173158287-A-G

159207225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173158276-A-G

http://identifiers.org/hco/1/GRCh38#159207353-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173158173-A-C

159207543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173157982-C-T

159207590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173157935-T-C

159207821-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: non coding transcript exon variant
orthologous variants: 173157699-A-T

159207869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: non coding transcript exon variant
orthologous variants: 173157650-T-C

http://identifiers.org/hco/1/GRCh38#159207907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173157612-C-A

159207907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: non coding transcript exon variant
orthologous variants: 173157612-C-T

159207912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40812
most severe consequence: non coding transcript exon variant
orthologous variants: 173157607-G-T