http://identifiers.org/hco/2/GRCh38#167814769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#67899101-C-A

167814769-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67899101-C-G

167814769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67899101-C-T

167814771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67899103-A-G

http://identifiers.org/hco/2/GRCh38#167814773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#67899105-C-A

167814773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67899105-C-T

167814817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67899148-T-C

http://identifiers.org/hco/2/GRCh38#167814877-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#67899218-A-C

167814877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67899218-A-G

http://identifiers.org/hco/2/GRCh38#167814888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#67899229-C-A

167814888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67899229-C-T

167814900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67899235-G-T

167814932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67899266-G-A

167814932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67899266-G-T

http://identifiers.org/hco/2/GRCh38#167814937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#67899271-C-A

167814989-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67899318-C-G

167814989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67899318-C-T

http://identifiers.org/hco/2/GRCh38#167815002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#67899327-C-A

167815002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67899327-C-T

167815003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67899328-T-C

167815009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67899331-A-G

167815023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67899345-G-T

167815048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67899371-G-T

http://identifiers.org/hco/2/GRCh38#167815170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#67899428-C-A

http://identifiers.org/hco/2/GRCh38#167815210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#67899458-C-A

167815210-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67899458-C-G

167815211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67899459-A-G

http://identifiers.org/hco/2/GRCh38#167815230-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#67899469-A-C

167815265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67899497-G-T

167815276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67899508-A-G

http://identifiers.org/hco/2/GRCh38#167815283-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#67899515-A-C

http://identifiers.org/hco/2/GRCh38#167815285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#67899517-C-A

167815285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67899517-C-T

167815301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67899533-T-C

167815301-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67899533-T-G

167815322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67899554-A-G

167815345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67899577-C-T

167815429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67899663-G-A

167815431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67899665-C-T

http://identifiers.org/hco/2/GRCh38#167815968-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#67900180-A-C

167816159-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67900358-C-G

167816170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67900368-G-A

167816241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67900473-G-T

167816745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67900977-A-G

167817075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67901295-C-T

167817081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67901301-T-C

167817120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67901339-T-C

167817120-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67901339-T-G

167817172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67901385-C-T

http://identifiers.org/hco/2/GRCh38#167817614-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#67902704-A-C

167817717-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67902823-C-G

167817787-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67902868-T-G

167817849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67902930-T-C

167818317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67903535-A-G

167818645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67903766-T-C

167818696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67903828-G-A

167818713-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67903845-T-G

167818760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67903889-G-A

167818760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67903889-G-T

167818971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67904057-C-T

167819402-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67904552-T-A

167819643-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67904791-A-T

167819986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67905098-G-A

167821058-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67906883-C-G

167821070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67909110-A-G

167821162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67909177-A-G

167821230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67909247-G-A

167821811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67909592-G-A

http://identifiers.org/hco/2/GRCh38#167821825-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#67909606-A-C

167821825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67909606-A-G

167821840-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67909621-T-G

167822085-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67909844-C-G

167822371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67910112-A-G

167822492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67910234-G-A

167822618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67910360-G-A

167822699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67910536-C-T

167822724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67910561-G-A

167822782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67910679-G-A

http://identifiers.org/hco/2/GRCh38#167822784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#67910681-C-A

167822784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67910681-C-T

167822910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67910798-T-C

167822914-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67910802-T-G

167822940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67910832-G-A

167822947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67910839-C-T

167822948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67910840-G-A

167822948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67910840-G-T

167823177-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67911050-G-C

167823215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67911093-G-T

167823280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67911155-G-A

167823569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67911458-A-G

167823606-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67911499-C-G

167823685-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67911578-T-A

167823685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67911578-T-C

167823776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67911673-C-T

167823875-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67911780-T-A

167824016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67913697-G-A

167824016-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67913697-G-C

167824098-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67913780-T-A

167824239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67913904-G-A

167825616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67915376-T-C

167825638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67915400-G-A

167825684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67915440-C-T

http://identifiers.org/hco/2/GRCh38#167825702-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#67915458-A-C

167825773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67915498-G-A

167825775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67915500-G-A

167826108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67915813-C-T

167826282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67915989-C-T

167826359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67916071-G-T

http://identifiers.org/hco/2/GRCh38#167826501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#67916216-C-A

http://identifiers.org/hco/2/GRCh38#167826544-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#67916237-A-C

167826545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67916238-C-T

167827648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67916528-G-A

167827817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67916696-C-T

167827820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67916699-A-G

167827955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67916827-C-T

167828140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67917169-C-T

167828279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67917295-G-A

167828364-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67917388-T-G

167828542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67917567-G-A

http://identifiers.org/hco/2/GRCh38#167828634-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#67917648-A-C

167828721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67917743-T-C

167828728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67917750-A-G

167828975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67917958-A-G

167829015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67917999-C-T

167829190-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67918169-A-T

167829706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67918473-C-T

167829794-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67918566-G-C

167829880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67918673-T-C

http://identifiers.org/hco/2/GRCh38#167829920-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#67918748-A-C

167829959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67918792-C-T

167829975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67918808-G-A

http://identifiers.org/hco/2/GRCh38#167830036-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#67918868-A-C

167830061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67918893-C-T

167830079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67918911-G-T

167830083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67918915-A-G

167830245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67919392-G-A

167830245-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67919392-G-C

167830440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67919563-G-A

167830529-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67919647-C-G

167830602-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67919701-G-C

167830871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67919957-G-A

167830871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67919957-G-T

167831089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67920419-A-G

167831377-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67920688-C-G

167831653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67920952-G-A

167831653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67920952-G-T

167831774-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67921056-G-C

167832209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67921346-G-A

167832429-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67921560-A-T

http://identifiers.org/hco/2/GRCh38#167832514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#67921638-C-A

167832514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67921638-C-T

167832879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67921980-G-A

167833050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67922162-G-A

167833208-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67922315-A-T

167833307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67922414-G-A

167833307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67922414-G-T

167833680-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67922746-G-C

167833750-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67922811-C-G

http://identifiers.org/hco/2/GRCh38#167833767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#67922828-C-A

http://identifiers.org/hco/2/GRCh38#167833979-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#67923029-A-C

http://identifiers.org/hco/2/GRCh38#167833983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#67923033-C-A

167834168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67923147-G-A

167834275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67923243-A-G

167841941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67923317-C-T

http://identifiers.org/hco/2/GRCh38#167842100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#67923509-C-A

167842348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67923758-G-A

167842517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67923907-G-A

167842932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67924002-T-C

http://identifiers.org/hco/2/GRCh38#167843254-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#67924294-A-C

167843320-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67924362-A-T

http://identifiers.org/hco/2/GRCh38#167843394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#67924427-C-A

167843428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67924460-G-A

167843511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67924543-C-T

167843669-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67924731-T-G

167843768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67924831-T-C

167843823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67924886-A-G

167843904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67924968-A-G

167844013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67925065-T-C

167844190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67925252-T-C

167851017-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67925292-A-T

http://identifiers.org/hco/2/GRCh38#167851025-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#67925300-A-C

http://identifiers.org/hco/2/GRCh38#167851242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#67925507-C-A

167851382-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67925618-T-A

http://identifiers.org/hco/2/GRCh38#167851906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#67925710-C-A

http://identifiers.org/hco/2/GRCh38#167851977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#67925773-C-A

167852678-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67926677-G-C

167852678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67926677-G-T

167852724-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67926735-C-G

167853368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67927406-A-G

167853399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67927420-C-T

167853447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67927467-G-A

167853555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67927575-G-A

167853676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67927989-G-T

167853683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67927996-T-C

167853715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67928028-T-C

167853767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67928078-G-A

167853852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67928162-G-A

167853852-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67928162-G-C

167854084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67928355-T-C

167854086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67928357-G-A

http://identifiers.org/hco/2/GRCh38#167854294-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#67928545-A-C

167854789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67928945-G-A

167854789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67928945-G-T

167855012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67929146-G-A

167855081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67929227-C-T

167855525-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67930462-G-C

167855821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67930758-C-T

167856143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67931065-G-A

167856387-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67931298-C-G

167856451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67931360-C-T

167856598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67931425-G-A

167856598-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67931425-G-C

167856600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67931427-G-T

167856807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67931571-T-C

167856837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67931598-G-T

167856838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67931599-G-T

167857242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67931965-G-A

167857275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67931998-T-C

167857326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67932038-C-T

167857421-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67932128-T-A

167857421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67932128-T-C

167857424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67932131-G-A

167857436-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67932139-C-G

http://identifiers.org/hco/2/GRCh38#167857558-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#67932277-A-C

167857707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67932427-G-A

http://identifiers.org/hco/2/GRCh38#167857940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#67932656-C-A

http://identifiers.org/hco/2/GRCh38#167857973-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#67932677-A-C

167857973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67932677-A-G

167858024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67932734-G-A

167858164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67932870-T-C

167858231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67932967-C-T

167858495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67933512-T-C

http://identifiers.org/hco/2/GRCh38#167858707-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#67933714-A-C

167858962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67933989-T-C

167859356-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67934374-A-T

167860084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67935147-T-C

167860223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67935259-T-C

167862592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67940940-G-A

167862594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67940942-G-A

167862626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67940974-C-T

http://identifiers.org/hco/2/GRCh38#167862627-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#67940975-C-A

http://identifiers.org/hco/2/GRCh38#167863179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#67941550-C-A

167863179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67941550-C-T

167863206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67941577-T-C

167863260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67941639-G-A

167863506-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67942027-C-G

167863838-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67942369-T-A

167863955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67942476-G-A

167864030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67942509-G-A

167864132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67942611-T-C

167864152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67942621-T-C

167864206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67942689-G-A

167864506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67942855-G-A

167864661-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67942913-T-G

167864786-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67943038-T-G

167864913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67943129-G-A

http://identifiers.org/hco/2/GRCh38#167865007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#67943178-C-A

167865018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67943185-T-C

167865386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67943534-G-A

167865386-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67943534-G-C

167865797-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67943833-C-G

167865910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67943948-G-T

167866290-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67944279-C-G

http://identifiers.org/hco/2/GRCh38#167866625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#67944899-C-A

167866625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67944899-C-T

167866710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67944973-G-A

167866710-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67944973-G-C

167866722-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67944982-G-C

167866846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67945097-G-A

167866893-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67945144-T-A

167867480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67945660-C-T

167867552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67945715-T-C

167867671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67945749-G-A

167867740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67945810-G-T

167867807-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67945879-G-C

167868020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67946110-G-A

167868248-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67947198-A-T

167868286-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67947224-C-G

167868286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67947224-C-T

167868530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67947790-T-C

167868530-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67947790-T-G

167868569-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67947827-T-G

167868690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67947936-A-G

167868887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67948132-G-A

167868887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67948132-G-T

167868900-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67948145-G-C

167868900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67948145-G-T

167868930-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67948176-C-G

167868930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67948176-C-T

http://identifiers.org/hco/2/GRCh38#167869492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#67948739-C-A

167869492-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67948739-C-G

167869492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67948739-C-T

167869555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67948802-T-C

167869837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 67949084-A-G

http://identifiers.org/hco/2/GRCh38#167869936-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#67949183-A-C

167870076-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67949317-G-C

167870076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67949317-G-T

167870107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67949351-G-A

167870212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67949452-G-T

167870227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67949466-T-C

http://identifiers.org/hco/2/GRCh38#167870260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#67949500-C-A

167870538-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67949785-A-T

http://identifiers.org/hco/2/GRCh38#167870754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#67949975-C-A

http://identifiers.org/hco/2/GRCh38#167871086-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#67950325-C-A

167871086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67950325-C-T

167871239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67950491-T-C

167871549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67950809-A-G

167871553-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67950813-G-C

167871659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67950898-G-A

167871659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67950898-G-T

167872320-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67951223-C-G

167872320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67951223-C-T

167872425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67951276-G-T

http://identifiers.org/hco/2/GRCh38#167872466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#67951317-C-A

167872466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67951317-C-T

167872490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67951342-G-T

167872510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67951361-A-G

167872527-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67951378-A-T

http://identifiers.org/hco/2/GRCh38#167872796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#67951653-C-A

167872796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67951653-C-T

167873594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67952581-G-A

167873594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67952581-G-T

167873616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67952603-A-G

167873786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67952768-G-T

167874067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67953056-G-T

167874108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67953090-G-T

http://identifiers.org/hco/2/GRCh38#167874110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#67953092-C-A

167874110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67953092-C-T

167874184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67953161-A-G

167874482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67953459-A-G

167874531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67953507-A-G

167875139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67953738-T-C

167876449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67954329-A-G

167876456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67954336-C-T

167876528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67954412-C-T

167876968-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67954923-G-C

167877099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67955028-G-T

167877348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67955272-G-A

167877404-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67955346-A-T

167877433-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67955366-T-A

167877598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67955520-A-G

167878270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67955764-T-C

167878291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67955789-C-T

167878296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67955792-T-C

167878407-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67955910-A-T

167878501-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67956000-C-G

167878577-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67956048-T-A

167878586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67956057-T-C

167878597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67956068-A-G

167878611-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67956075-C-G

167878840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67956249-G-A

167879636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67957897-G-T

167879826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67958039-A-G

167880346-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67958307-C-G

167880346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67958307-C-T

167880496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67958401-T-C

167880615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67958510-A-G

http://identifiers.org/hco/2/GRCh38#167880687-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#67958575-A-C

167880703-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67958591-G-C

167880763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67958650-C-T

167880787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67958673-G-A

http://identifiers.org/hco/2/GRCh38#167880789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#67958675-C-A

http://identifiers.org/hco/2/GRCh38#167881099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#67958963-C-A

167881496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67959351-G-A

167881496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67959351-G-T

http://identifiers.org/hco/2/GRCh38#167881597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#67959448-C-A

167881629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67959467-G-A

167881806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67959645-G-T

167882050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67959876-G-A

167882050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67959876-G-T

http://identifiers.org/hco/2/GRCh38#167882368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#67968953-C-A

167882392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67968977-G-A

167882434-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67969019-C-G

167882434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67969019-C-T

167882491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67969076-C-T

167882860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67969446-T-C

167883041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67969627-T-C

167895776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67972933-G-A

167896419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67973538-G-A

167896448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67973602-G-A

167896571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67973782-C-T

167896611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67973826-A-G

http://identifiers.org/hco/2/GRCh38#167898393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#67975059-C-A

167898393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67975059-C-T

167898736-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67975430-A-T

167898944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67975637-C-T

167899372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67976054-G-A

167899372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67976054-G-T

167899703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67976384-G-T

167899727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67976406-C-T

167899871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67976539-G-A

167899975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67976650-G-T

167900331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67976985-G-T

167900540-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67977357-A-T

167905691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67978592-C-T

167905732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67978633-G-A

167905913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67978825-A-G

http://identifiers.org/hco/2/GRCh38#167906017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#67978930-C-A

167906017-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67978930-C-G

167906017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67978930-C-T

167906120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67979031-G-A

167906214-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67979130-T-A

http://identifiers.org/hco/2/GRCh38#167906301-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#67979212-A-C

http://identifiers.org/hco/2/GRCh38#167906749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-A

167906749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

167907603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67980535-T-C

167907646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67980555-A-G

167907660-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67980568-G-C

http://identifiers.org/hco/2/GRCh38#167907696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#67980602-C-A

167907791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67980697-T-C

http://identifiers.org/hco/2/GRCh38#167907796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#67980702-C-A

167907811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67980717-G-A

167907811-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67980717-G-C

167907832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67980738-G-A

167908013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67980887-G-A

167908030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67980906-A-G

167908037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67980913-G-A

167908072-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67980944-C-G

167908115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67980989-G-A

167908320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67981203-G-T

167909238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67981542-C-T

167909278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67981601-G-A

167909463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67981781-C-T

http://identifiers.org/hco/2/GRCh38#167909514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#67981832-C-A

167909714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67982009-G-A

167909714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67982009-G-T

167909715-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67982010-T-A

http://identifiers.org/hco/2/GRCh38#167909910-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#67982182-A-C

167909910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67982182-A-G

167910067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67982328-T-C

http://identifiers.org/hco/2/GRCh38#167910125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#67982384-C-A

167910125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67982384-C-T

167910234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67982472-G-A

167910333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67982579-A-G

167910430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67982654-C-T

167912416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67987383-G-A

167912490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67987446-A-G

167912768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67987704-G-A

167912950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67987870-G-A

167913139-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67988042-G-C

167913165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67988069-C-T

167913276-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67988178-G-C

167913281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67988183-G-A

167913368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67988266-G-A

167913637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67989656-G-A

167914885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67990809-C-T

167914899-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67990825-G-C

167915179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67991113-A-G

http://identifiers.org/hco/2/GRCh38#167915369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#67991320-C-A

167915469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67991392-G-A

167915962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67991852-G-A

167916307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67992151-G-A

167916619-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67992473-C-G

167916661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67992517-C-T

167916691-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67992549-T-A

167917768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67993932-C-T

167917864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67994025-C-T

http://identifiers.org/hco/2/GRCh38#167919968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#67995941-C-A

167924887-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68000728-A-T

167924905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68000746-G-A

167924905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68000746-G-T

http://identifiers.org/hco/2/GRCh38#167925097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#68000907-C-A

167925123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68000933-T-C

167925429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68001346-C-T

167925541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68001436-G-A

http://identifiers.org/hco/2/GRCh38#167925633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#68001512-C-A

http://identifiers.org/hco/2/GRCh38#167925697-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#68001575-A-C

167925781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68001658-G-A

http://identifiers.org/hco/2/GRCh38#167925950-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#68001820-A-C

167925950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68001820-A-G

167926247-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68002093-C-G

167926471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68002252-A-G

167926512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68002292-G-A

167926646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68002375-A-G

http://identifiers.org/hco/2/GRCh38#167926803-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#68002550-A-C

167926844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68002598-A-G

167927472-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68002652-T-A

167927472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68002652-T-C

167927871-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68003024-G-C

167928280-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68004552-A-T

167928931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68005316-G-A

167929117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68005501-G-A

167929117-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68005501-G-C

167929211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68005595-G-A

167929263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68005647-T-C

167929828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68006209-T-C

167929947-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68006333-G-C

167930193-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68006560-T-A

167930201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68006567-T-C

167930334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68006690-G-A

http://identifiers.org/hco/2/GRCh38#167930410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#68006766-C-A

167930416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68006772-A-G

167930618-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68006999-T-A

167930872-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68008697-T-G

167930963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68008778-T-C

167931071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68008877-G-A

167931126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68008928-C-T

167931367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68009167-A-G

167931385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68009185-C-T

http://identifiers.org/hco/2/GRCh38#167931481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#68009296-C-A

167931499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68009326-A-G

http://identifiers.org/hco/2/GRCh38#167932031-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#68009790-A-C

167932031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68009790-A-G

167932114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68009873-C-T

167936691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68013874-C-T

167937102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68014290-G-A

167937139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68014327-A-G

167937141-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68014329-C-G

167937141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68014329-C-T

167937268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68014451-T-C

167937496-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68014633-T-A

http://identifiers.org/hco/2/GRCh38#167937817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#68014806-C-A

167938643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68019619-T-C

167938705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68019670-G-A

167938708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68019673-T-C

167938786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68019751-A-G

167939033-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68019985-A-T

167939132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68020087-G-A

167939132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68020087-G-T

167939335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68020272-G-A

167939384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68020321-A-G

167939406-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68020342-C-G

167939406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68020342-C-T

167939676-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68020606-A-T

167939766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68020687-T-C

167939872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68020791-G-T

167939951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68020875-T-C

167940073-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68020995-T-A

167940374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68021301-G-A

http://identifiers.org/hco/2/GRCh38#167940406-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#68021333-A-C

167940940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40089
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68021840-G-A