http://identifiers.org/hco/9/GRCh38#132725722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28703041-C-A

132725722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 28703041-C-T

http://identifiers.org/hco/9/GRCh38#132725764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28702999-C-A

132725951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28702820-G-A

132725951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28702820-G-T

http://identifiers.org/hco/9/GRCh38#132725994-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28702807-A-C

132725994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28702807-A-G

132725994-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28702807-A-T

132726031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28702768-A-G

132726050-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28702749-T-A

132726050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28702749-T-C

132726050-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28702749-T-G

132726067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28702741-G-A

132726067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28702741-G-T

http://identifiers.org/hco/9/GRCh38#132726076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28702732-C-A

132726076-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28702732-C-G

132726076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28702732-C-T

132726087-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28702725-T-A

http://identifiers.org/hco/9/GRCh38#132727248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28699962-C-A

http://identifiers.org/hco/9/GRCh38#132727339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28699878-C-A

132727339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28699878-C-T

132727400-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28699803-G-C

132727400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28699803-G-T

132727424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28699780-A-G

132727556-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28699652-T-G

132727562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28699646-T-C

132727692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28699560-T-C

http://identifiers.org/hco/9/GRCh38#132727705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28699547-C-A

132727705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28699547-C-T

132727719-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28699533-T-A

132727719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28699533-T-C

132727719-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28699533-T-G

132727992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28699355-G-A

132728085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28699294-A-G

132728103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28699275-G-A

132728126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28699251-G-A

132728127-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28699250-T-A

http://identifiers.org/hco/9/GRCh38#132728139-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28699237-A-C

132728141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28699235-G-A

132743899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28689014-G-A

132744365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28688586-G-A

132744447-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28688543-T-G

http://identifiers.org/hco/9/GRCh38#132744531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28688468-C-A

132744997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28687991-C-T

132745367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28687610-G-T

132745427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28687550-G-A

132745427-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28687550-G-C

132746058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28686910-T-C

132746199-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28686791-A-T

132746329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28686645-C-T

132746330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28686644-G-A

132746382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28686583-G-A

132746451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28686529-T-C

http://identifiers.org/hco/9/GRCh38#132746810-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28686191-A-C

http://identifiers.org/hco/9/GRCh38#132746825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28686176-C-A

132746825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28686176-C-T

132748148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28684700-T-C

132748150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28684698-T-C

132748197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28684652-G-A

132748197-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28684652-G-C

132748351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28684443-G-A

http://identifiers.org/hco/9/GRCh38#132748376-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28684419-A-C

132748401-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28684398-G-C

132748487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28684332-C-T

132748518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28684301-A-G

http://identifiers.org/hco/9/GRCh38#132748590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28684237-C-A

132749843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28679565-G-A

132749850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28679558-C-T

132749851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28679557-G-A

132749988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28679404-T-C

132757073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28676973-T-C

132757133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28676913-T-C

132757293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28676775-C-T

132757310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28676758-C-T

132757365-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28676702-C-G

132757636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28676476-T-C

132758101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28675408-A-G

132768763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28671267-T-C

http://identifiers.org/hco/9/GRCh38#132768944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28671104-C-A

132768944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28671104-C-T

132769051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28671028-G-T

132769083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28671002-G-A

132769083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28671002-G-T

http://identifiers.org/hco/9/GRCh38#132769096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28670997-C-A

132769109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28670984-G-A

132769109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28670984-G-T

http://identifiers.org/hco/9/GRCh38#132769111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28670982-C-A

132769111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28670982-C-T

132769153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28670973-G-A

132769153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28670973-G-T

132769162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28670959-G-T

132769164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28670957-A-G

http://identifiers.org/hco/9/GRCh38#132769185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28670940-C-A

132769185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28670940-C-T

132769197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28670928-G-A

132769197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28670928-G-T

http://identifiers.org/hco/9/GRCh38#132769274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28670867-C-A

132769274-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28670867-C-G

132769280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28670861-T-C

132769284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28670857-T-C

132769396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28670752-G-T

132769439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28670719-C-T

132769440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28670718-G-A

132769440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28670718-G-T

http://identifiers.org/hco/9/GRCh38#132769609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28670571-C-A

132769619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 28670562-C-T

132769642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28670548-C-T

132769714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28670494-A-G

132769801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28670408-T-C

132769827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28670383-A-G

132769827-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28670383-A-T

132769925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28670293-T-C

132769937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28670281-G-A

132769937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28670281-G-T

http://identifiers.org/hco/9/GRCh38#132770275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28669978-C-A

http://identifiers.org/hco/9/GRCh38#132770289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28669964-C-A

132770389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28669863-G-A

132770538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28669747-G-A

132770538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28669747-G-T

132773448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28668516-C-T

132773746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28668357-G-A

http://identifiers.org/hco/9/GRCh38#132774148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28668064-C-A

132774197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28668013-G-A

http://identifiers.org/hco/9/GRCh38#132775007-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28667270-A-C

132775020-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28667258-T-G

132775823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28666418-T-C

132775891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28666357-A-G

132776313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28665970-C-T

132776420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28665833-G-A

132778165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28664415-C-T

132778650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28663893-G-T

132778686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28663845-G-A

132778705-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28663826-T-G

132780342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28662260-G-A

132781301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28661421-T-C

132781865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28660827-C-T

132781894-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28660798-A-T

132782019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28660674-T-C

132782307-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28660379-T-G

132783648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28656828-A-G

http://identifiers.org/hco/9/GRCh38#132783936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28656528-C-A

132783936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28656528-C-T

132783954-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28656510-T-G

132784284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28656337-T-C

132784320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28656302-A-G

132784612-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28656065-A-T

132784624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28656053-G-T

132784757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28655954-G-A

132792485-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28650210-A-T

132792486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28650209-T-C

132792486-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28650209-T-G

132792577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28650131-G-A

132792577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28650131-G-T

132792610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28650109-G-A

132792610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28650109-G-T

http://identifiers.org/hco/9/GRCh38#132792706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28650021-C-A

132792706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 28650021-C-T

132793324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28649046-T-C

132793391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28649001-G-A

132793430-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28648969-A-T

132793759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28648662-C-T

132793974-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28648470-G-C

132798104-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28647250-G-C

132798198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28647134-G-A

132798673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28646686-C-T

http://identifiers.org/hco/9/GRCh38#132798677-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28646682-A-C

132798701-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28646639-T-G

132799717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28646269-A-G

132799746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28646243-A-G

132799754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28646235-C-T

132799758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28646231-C-T

132800275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28645717-C-T

132800286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28645706-G-A

http://identifiers.org/hco/9/GRCh38#132805065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28642883-C-A

132805068-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28642882-T-G

132805238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28642694-T-C

132805852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28642127-G-A

132806570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28641350-T-C

132806775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28641135-G-A

132807129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28640814-T-C

132807131-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28640812-T-G

132807240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28640738-G-A

132807382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28640595-C-T

132807389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28640588-G-T

132807390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28640587-C-T

132807481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28640484-C-T

132807825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28640115-C-T

132807949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28639990-G-A

132807949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28639990-G-T

http://identifiers.org/hco/9/GRCh38#132808196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28639759-C-A

132808228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28639733-C-T

132808269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28639704-C-T

132808302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28639671-T-C

132808736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28639268-G-A

132808835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28639164-C-T

132809908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28636950-T-C

132810004-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28636901-C-G

132810041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28636866-C-T

132810276-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28636642-T-A

132810519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28636464-G-A

132810587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28636423-T-C

132810635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28636377-C-T

132814471-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28632886-G-C

132814471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28632886-G-T

132814487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28632868-G-A

132814487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28632868-G-T

http://identifiers.org/hco/9/GRCh38#132814523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28632849-C-A

132814722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 28632675-A-G

132814917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28632494-T-C

132814927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28632483-A-G

132815052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28632359-C-T

132815102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28632311-G-A

132822447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28630289-G-A

132822447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28630289-G-T

http://identifiers.org/hco/9/GRCh38#132822485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28630255-C-A

132822485-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28630255-C-G

132822485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28630255-C-T

132822957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28629892-G-A

132823062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28629789-G-A

132823062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28629789-G-T

http://identifiers.org/hco/9/GRCh38#132823066-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28629785-A-C

132823066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28629785-A-G

132823066-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28629785-A-T

http://identifiers.org/hco/9/GRCh38#132823150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28629712-C-A

132823216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 28629663-C-T

132823235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 28629644-G-A

132823236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 28629643-G-A

132823489-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28629416-G-C

132823656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28629246-T-C

132824047-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28628867-G-C

132824241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28628696-C-T

http://identifiers.org/hco/9/GRCh38#132825347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28627589-C-A

132825347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28627589-C-T

132826725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28625851-T-C

http://identifiers.org/hco/9/GRCh38#132826808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28625755-C-A

132826808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28625755-C-T

132826812-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28625751-C-G

132826907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 28625660-T-C

132826932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 28625635-C-T

http://identifiers.org/hco/9/GRCh38#132827060-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28625507-A-C

132827071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28625496-G-A

http://identifiers.org/hco/9/GRCh38#132827185-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28625382-A-C

132827576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28624886-G-A

132827576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28624886-G-T

132827683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28624747-G-A

132827710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28624722-G-A

132827710-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28624722-G-C

132827710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28624722-G-T

http://identifiers.org/hco/9/GRCh38#132827718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28624714-C-A

132827718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28624714-C-T

http://identifiers.org/hco/9/GRCh38#132827726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28624698-C-A

132827726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28624698-C-T

http://identifiers.org/hco/9/GRCh38#132827727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28624697-C-A

132827727-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28624697-C-G

132827730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28624694-T-C

132827813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28624594-A-G

http://identifiers.org/hco/9/GRCh38#132827830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28624580-C-A

132827830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28624580-C-T

http://identifiers.org/hco/9/GRCh38#132827887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28624535-C-A

132827887-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28624535-C-G

132827887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28624535-C-T

132827892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28624530-T-C

http://identifiers.org/hco/9/GRCh38#132827987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28624471-C-A

132828006-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 28624462-G-C

132828006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 28624462-G-T

http://identifiers.org/hco/9/GRCh38#132828007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28624461-C-A

132828007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28624461-C-T

132828117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28624353-A-G

132828133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28624338-G-A

132828133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28624338-G-T

132828407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28624146-T-C

132828420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28624127-T-C

http://identifiers.org/hco/9/GRCh38#132828504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28624050-C-A

132828707-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 28623836-A-T

132828738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28623805-A-G

http://identifiers.org/hco/9/GRCh38#132828741-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28623802-C-A

132828741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28623802-C-T

http://identifiers.org/hco/9/GRCh38#132828754-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28623789-A-C

132828767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28623772-T-C

http://identifiers.org/hco/9/GRCh38#132830912-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28620983-A-C

132830912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28620983-A-G

132830922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28620972-T-C

http://identifiers.org/hco/9/GRCh38#132831284-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28620627-A-C

132831291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28620620-G-A

132831291-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28620620-G-C

132831559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28620327-G-A

132831700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28620189-A-G

132831932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28619973-C-T

http://identifiers.org/hco/9/GRCh38#132831970-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28619936-A-C

132831970-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28619936-A-T

132832032-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28619889-T-A

132832040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28619881-T-C

132832066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28619855-A-G

132832068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28619853-A-G

132832150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28619664-A-G

132832150-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28619664-A-T

132832445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28619391-T-C

132832672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28618946-T-C

132832872-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28618642-T-G

132833732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28617920-A-G

132833770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28617883-G-A

132833789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28617864-G-A

132833793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28617860-C-T

132833905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28617751-T-C

132834053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28617617-T-C

132843790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28611629-G-T

132843796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28611623-T-C

132843808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28611606-G-A

132843889-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28611474-A-T

http://identifiers.org/hco/9/GRCh38#132843891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28611472-C-A

132844040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28611339-A-G

132844098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28611289-C-T

132844371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28611045-A-G

132844389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28611038-C-T

132844746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28610674-T-C

132845316-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28610159-C-G

132845757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28609847-G-A

132845821-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28609816-A-T

132845834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28609803-C-T

132845905-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28609741-A-T

132846007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28609494-A-G

132846240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28609269-C-T

132846242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28609267-C-T

132846245-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28609264-C-G

132854770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28606588-G-A

132854770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28606588-G-T

132854787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28606577-G-A

132854842-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28606517-T-G

132854872-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 28606480-C-G

132854947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28606408-G-A

132854978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28606378-C-T

132857521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28605499-C-T

132857873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28605193-G-A

132858063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28605003-C-T

132858221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28604888-A-G

132863682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 28602381-G-A

132863787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28602276-A-G

http://identifiers.org/hco/9/GRCh38#132866773-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28600106-A-C

132866773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28600106-A-G

132866813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28600072-T-C

132866861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28600026-A-G

132867646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28599351-C-T

132867907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28599276-A-G

132868076-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28599113-C-G

132868087-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28599102-G-C

132868123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28599069-G-A

132868138-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28599054-G-C

132868632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28598648-G-A

132868961-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28598238-T-G

132869034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28598124-G-A

http://identifiers.org/hco/9/GRCh38#132869450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28597714-C-A

132869450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28597714-C-T

132869473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28597700-G-A

132869538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28597654-C-T

132869579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28597614-G-A

132869902-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28597294-G-C

132869916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28597286-C-T

132870031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28597182-G-A

http://identifiers.org/hco/9/GRCh38#132870111-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28597092-A-C

132870732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28596493-G-A

132870744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28596481-C-T

http://identifiers.org/hco/9/GRCh38#132870832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28596417-C-A

132870838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28596409-C-T

132871970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28595818-C-T

132874351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28593456-T-C

132874370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28593438-T-C

132874430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28593395-T-C

132874559-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28593273-T-G

132874974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28592859-G-A

132874974-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28592859-G-C

132874974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28592859-G-T

132875008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28592826-G-A

132875008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28592826-G-T

132875123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28592775-T-C

132875176-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28592722-G-C

132875237-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 28592663-T-A

132875579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28592462-C-T

132875745-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28592344-C-G

132875747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28592342-G-A

132876200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28591975-G-A

132877734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28590914-C-T

132877808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28590843-G-T

132877828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28590828-C-T

132877850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28590799-C-T

132877896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28590753-G-T

http://identifiers.org/hco/9/GRCh38#132878082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#28590436-C-A

132878082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28590436-C-T

http://identifiers.org/hco/9/GRCh38#132878114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28590404-C-A

132878114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28590404-C-T

132878190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 28590266-G-A

132878190-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 28590266-G-C

132878220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 28590236-G-A

132878220-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 28590236-G-C

132878220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 28590236-G-T

132878273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 28590185-C-T

132878414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 28590091-G-A

132878414-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 28590091-G-C

132878414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 28590091-G-T

132878489-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 28590049-G-C

http://identifiers.org/hco/9/GRCh38#132878591-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28589993-A-C

132878662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 28589897-G-A

132878662-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 28589897-G-C

132878662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 28589897-G-T

132878706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 28589853-C-T

132878708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 28589851-T-C

132878717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 28589839-T-C

132878736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28589823-T-C

132878755-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28589806-C-G

132878755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28589806-C-T

132878778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28589783-G-A

132878778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28589783-G-T

http://identifiers.org/hco/9/GRCh38#132878825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#28589767-C-A

132878825-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28589767-C-G

132878825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28589767-C-T

http://identifiers.org/hco/9/GRCh38#132878861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#28589731-C-A

132878861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28589731-C-T

http://identifiers.org/hco/9/GRCh38#132878880-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28589712-C-A

http://identifiers.org/hco/9/GRCh38#132878927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28589676-C-A

http://identifiers.org/hco/9/GRCh38#132878929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28589674-C-A

132878934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28589669-T-C

132878940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28589663-G-A

132878940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28589663-G-T

http://identifiers.org/hco/9/GRCh38#132878970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28589636-C-A

132878970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28589636-C-T

http://identifiers.org/hco/9/GRCh38#132878998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28589608-C-A

132879024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26526
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28589582-G-T