51542058-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7590517-T-A

51542150-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7590432-G-C

51542187-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7590397-G-C

51542201-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7590395-G-C

51542217-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7590379-C-G

51542249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7590369-C-T

http://identifiers.org/hco/8/GRCh38#51542391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#7590215-C-A

51542843-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7588543-T-A

51543089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7588325-C-T

51543110-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7588304-T-G

51543355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7587626-T-C

http://identifiers.org/hco/8/GRCh38#51543401-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#7587577-A-C

51586204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7585621-G-T

51586210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7585615-G-A

51586832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7584822-G-T

51587039-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7584641-G-T

51587470-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7584291-C-G

51587623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7584139-T-C

http://identifiers.org/hco/8/GRCh38#51587695-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#7584069-A-C

51587739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7584019-T-C

51587760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7583998-T-C

51587884-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7583886-T-G

51588091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7583730-G-A

51588492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7583365-G-A

http://identifiers.org/hco/8/GRCh38#51591568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#7582921-C-A

51592494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7581727-G-A

51617757-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7561515-A-T

51617807-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7561469-C-G

51618033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7561277-G-A

51618126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7561177-A-G

51618325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7561030-A-G

51618513-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7560852-T-G

51618640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7560730-C-T

51618713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7560656-T-C

http://identifiers.org/hco/8/GRCh38#51618721-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#7560648-A-C

http://identifiers.org/hco/8/GRCh38#51618921-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#7560503-A-C

http://identifiers.org/hco/8/GRCh38#51620284-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#7560267-A-C

51620284-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7560267-A-T

51620309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7560242-G-A

51620391-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7560161-T-A

51620958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7546013-G-A

51620958-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7546013-G-C

51620980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7545991-T-C

51621084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7545898-G-T

51621225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7545755-C-T

51621299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7545671-A-G

51621329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7545642-A-G

http://identifiers.org/hco/8/GRCh38#51621727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#7545412-C-A

51622409-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7544753-T-G

51622817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7540402-C-T

51622894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7540341-C-T

51623067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7540185-T-C

51623114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7540138-C-T

51623164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7540095-A-G

51623196-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7540061-C-G

51623201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7540056-G-A

51623421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7539865-C-T

http://identifiers.org/hco/8/GRCh38#51624074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#7539485-C-A

http://identifiers.org/hco/8/GRCh38#51624083-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#7539476-A-C

http://identifiers.org/hco/8/GRCh38#51624128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#7539444-C-A

51624147-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7539433-T-A

51624742-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7538819-G-C

51625732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7537651-T-C

http://identifiers.org/hco/8/GRCh38#51626465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#7536632-C-A

51626563-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7536541-C-G

51626783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7536164-T-C

http://identifiers.org/hco/8/GRCh38#51647481-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#7520679-A-C

51647775-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7520433-T-G

51647778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7520430-T-C

51647937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7520277-A-G

51647948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7520266-A-G

51648000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7520217-C-T

51648234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7520008-C-T

51648248-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7519994-T-G

51648330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7519912-G-A

51648841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7518754-T-C

51649386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7518206-T-C

51651921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7502814-C-T

51651955-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7502780-T-G

51651974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7502750-G-A

51652068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7502654-T-C

51652095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7502627-G-A

51652129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7502591-G-T

51652162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7502563-G-T

http://identifiers.org/hco/8/GRCh38#51652221-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#7502508-A-C

51652221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7502508-A-G

51652245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7502485-G-A

51652245-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7502485-G-C

http://identifiers.org/hco/8/GRCh38#51652330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#7502401-C-A

51652421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7502333-T-C

51653031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7501944-C-T

51653904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7501410-C-T

51653948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7501357-T-C

51654146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7501171-A-G

51654274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7501100-G-A

51654289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7501082-A-G

51654309-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7501062-G-T

51654514-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7500879-G-C

http://identifiers.org/hco/8/GRCh38#51654596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#7500805-C-A

51654601-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7500800-C-G

51654601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7500800-C-T

51654666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7500732-A-G

http://identifiers.org/hco/8/GRCh38#51654668-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#7500730-A-C

51654668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7500730-A-G

51654670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7500728-A-G

51654673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7500725-A-G

http://identifiers.org/hco/8/GRCh38#51654675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#7500723-C-A

51654675-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7500723-C-G

51654675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7500723-C-T

http://identifiers.org/hco/8/GRCh38#51654722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#7500680-C-A

51654722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 7500680-C-T

51654785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7500618-C-T

51654894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7500530-G-T

51656073-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7500215-T-A

51656179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7500092-A-G

51656580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7498203-A-G

51656604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7498180-A-G

51656684-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7498100-G-C

51656767-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7498044-T-G

51657415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7497584-T-C

51657549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7497474-T-C

51657700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7497353-G-A

51657810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7497240-A-G

51658710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7496649-T-C

51661790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7492062-A-G

51664621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7490572-A-G

51664676-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7490514-G-C

http://identifiers.org/hco/8/GRCh38#51664763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#7490419-C-A

51664763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7490419-C-T

51664825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7490358-C-T

http://identifiers.org/hco/8/GRCh38#51665048-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#7490174-A-C

51666547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7489024-A-G

51666911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7488681-A-G

51667477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7488193-G-A

51667477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7488193-G-T

51667838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7487892-C-T

51667848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7487882-G-A

51701277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7388976-A-G

http://identifiers.org/hco/8/GRCh38#51701326-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#7389024-A-C

51701598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7389296-C-T

51716167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7383766-T-C

51716201-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7383733-T-A

51716257-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7383678-T-A

51716437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7383515-C-T

51716455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7383497-A-G

51716472-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7383479-C-G

51716492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7383459-A-G

http://identifiers.org/hco/8/GRCh38#51716621-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#7383301-A-C

51716623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7383299-G-A

51716822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7383116-G-A

51716834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7383102-G-A

51716888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7383068-C-T

51725106-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7349172-T-A

http://identifiers.org/hco/8/GRCh38#51725145-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#7349117-A-C

51725244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7349012-C-T

http://identifiers.org/hco/8/GRCh38#51725246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#7349010-C-A

51725249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7349007-G-A

51725538-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7348735-T-A

http://identifiers.org/hco/8/GRCh38#51725712-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#7348562-A-C

51725712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7348562-A-G

51725754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7348521-T-C

51725785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7348489-G-A

51725785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7348489-G-T

51725813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7348447-G-T

51725949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7348333-G-A

51726055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7348231-G-T

51726115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7348174-G-A

51726273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7341818-A-G

51726511-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7341278-A-T

51726634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7341182-T-C

51726635-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7341181-T-A

51726696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7341129-C-T

51726755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7341080-A-G

http://identifiers.org/hco/8/GRCh38#51726800-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#7341047-A-C

51726911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7340936-C-T

51726969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7340877-T-C

51727129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7340748-G-T

51773442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7320354-C-T

http://identifiers.org/hco/8/GRCh38#51773528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#7320281-C-A

51773528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7320281-C-T

51773689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7320132-T-C

51773754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7320072-T-C

51773814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7320011-C-T

51773853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7319955-C-T

http://identifiers.org/hco/8/GRCh38#51774322-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#7317645-A-C

http://identifiers.org/hco/8/GRCh38#51774881-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#7317266-A-C

http://identifiers.org/hco/8/GRCh38#51774992-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#7317171-A-C

51778585-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7314231-A-T

51778619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7314202-C-T

http://identifiers.org/hco/8/GRCh38#51778730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#7314121-C-A

51778784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7314068-C-T

51778800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7314050-G-A

http://identifiers.org/hco/8/GRCh38#51778826-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#7314025-A-C

http://identifiers.org/hco/8/GRCh38#51778858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#7313993-C-A

http://identifiers.org/hco/8/GRCh38#51779091-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#7313595-A-C

51779150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7313542-T-C

51779323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7313376-C-T

51779393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7313331-C-T

51806407-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7294842-G-T

51806869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7294444-T-C

51807674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7294058-G-A

51807682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7294050-C-T

51807964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7293789-C-T

51807984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7293765-A-G

http://identifiers.org/hco/8/GRCh38#51808058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#7293692-C-A

51808060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7293690-A-G

51808205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7293561-T-C

51808436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7293283-C-T

http://identifiers.org/hco/8/GRCh38#51808765-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#7292824-A-C

51808765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7292824-A-G

51808893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7292694-G-A

http://identifiers.org/hco/8/GRCh38#51809298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#7292231-C-A

51809352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26359
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 7292177-T-C