79236181-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: 5 prime UTR variant
orthologous variants: 93636195-G-C

79236181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: 5 prime UTR variant
orthologous variants: 93636195-G-T

79236227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: 5 prime UTR variant
orthologous variants: 93636145-G-A

79236227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: 5 prime UTR variant
orthologous variants: 93636145-G-T

79236233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: 5 prime UTR variant
orthologous variants: 93636140-G-A

79236233-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: 5 prime UTR variant
orthologous variants: 93636140-G-T

79236368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: 5 prime UTR variant
orthologous variants: 93636045-G-A

http://identifiers.org/hco/5/GRCh38#79236554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#93635894-C-A

79236554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: 5 prime UTR variant
orthologous variants: 93635894-C-T

http://identifiers.org/hco/5/GRCh38#79236720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#93635743-C-A

79236720-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: missense variant
orthologous variants: 93635743-C-G

79236720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: missense variant
orthologous variants: 93635743-C-T

79236836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: synonymous variant
orthologous variants: 93635627-G-A

79236836-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: synonymous variant
orthologous variants: 93635627-G-C

79236836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: synonymous variant
orthologous variants: 93635627-G-T

79236921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: missense variant
orthologous variants: 93635566-G-A

79236921-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: missense variant
orthologous variants: 93635566-G-C

http://identifiers.org/hco/5/GRCh38#79236966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#93635518-C-A

79236966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: missense variant
orthologous variants: 93635518-C-T

79237068-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: missense variant
orthologous variants: 93635419-C-G

79237068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: missense variant
orthologous variants: 93635419-C-T

79237095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: missense variant
orthologous variants: 93635392-A-G

79237233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: missense variant
orthologous variants: 93635257-G-A

79237233-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: missense variant
orthologous variants: 93635257-G-T

79237234-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: missense variant
orthologous variants: 93635256-T-A

79237254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: missense variant
orthologous variants: 93635236-G-A

79237284-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: missense variant
orthologous variants: 93635206-G-C

79237284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: stop gained
orthologous variants: 93635206-G-T

79237368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: missense variant
orthologous variants: 93635122-G-T

79237691-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: 93634801-G-C

79237698-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: 93634794-C-G

79237705-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: 93634787-T-G

79237712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: 93634780-T-C

79237718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: 93634774-T-C

79237718-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: 93634774-T-G

http://identifiers.org/hco/5/GRCh38#79237719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#93634773-C-A

79237719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: 93634773-C-T

79237747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: 93634755-G-A

79237747-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: 93634755-G-C

79237747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: 93634755-G-T

79237783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: 93634724-G-A

79237783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: 93634724-G-T

79237793-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: 93634714-T-A

79237793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: 93634714-T-C

http://identifiers.org/hco/5/GRCh38#79237829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#93634673-C-A

79237829-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: 93634673-C-G

http://identifiers.org/hco/5/GRCh38#79237881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#93634634-C-A

79238105-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: 93634435-T-G

79238165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: 93634375-T-C

79238438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: 93634114-A-G

79238564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: 93634017-C-T

79238994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: 93633925-C-T

79239078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: 93633855-T-C

79239179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: 93633765-A-G

79239403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: 93633418-A-G

79240160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: 93633038-C-T

79240169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: 93633029-C-T

79240645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: 93632852-A-G

79240667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: 93632832-A-G

79241054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: 93632273-A-G

79241079-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: 93632257-C-G

79262073-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: 93623638-T-A

79262211-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: 93623511-C-G

79262247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: 93623483-G-A

http://identifiers.org/hco/5/GRCh38#79262781-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#93622984-A-C

79262781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: 93622984-A-G

79262875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: 93622903-T-C

79262997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: 93622817-A-G

79277910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 93609300-C-T

79277919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: missense variant
orthologous variants: 93609291-A-G

79277991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: missense variant
orthologous variants: 93609219-C-T

79278054-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: missense variant
orthologous variants: 93609156-C-G

79278122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: 93609080-T-C

79278203-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: 93608993-T-A

79278203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: 93608993-T-C

79280207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: 93608803-A-G

79280235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: 93608775-A-G

79280361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: 93608674-A-G

http://identifiers.org/hco/5/GRCh38#79280431-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#93608635-A-C

79280586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: 93608497-A-G

79280618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: 93608454-A-G

79280632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: 93608441-G-A

79280920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: 93608239-T-C

http://identifiers.org/hco/5/GRCh38#79280968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#93608213-C-A

79280968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: 93608213-C-T

79280977-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: 93608204-T-A

79285876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: 93604527-A-G

http://identifiers.org/hco/5/GRCh38#79285899-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#93604504-A-C

79285899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: 93604504-A-G

79285968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: 93604426-T-C

79286152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: 93604223-G-A

79286217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: 93604172-T-C

79286264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: 93604143-G-T

79286781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: 93603893-T-C

79286869-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: 93603798-A-T

79287124-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: 93603560-C-G

79289945-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: 93601395-G-C

79290020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: 93601329-G-A

79290020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: 93601329-G-T

79290027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: 93601322-A-G

79290060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: 93601265-G-A

79290109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: 93601235-T-C

79290121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 93601223-A-G

79290157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: missense variant
orthologous variants: 93601187-A-G

79290160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: missense variant
orthologous variants: 93601184-G-A

79290160-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: missense variant
orthologous variants: 93601184-G-C

79290160-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: stop gained
orthologous variants: 93601184-G-T

79290181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: missense variant
orthologous variants: 93601163-G-A

http://identifiers.org/hco/5/GRCh38#79291055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#93596375-C-A

79291055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: 93596375-C-T

79291120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: 93596305-T-C

79291195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: missense variant
orthologous variants: 93596230-G-A

79291267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: synonymous variant
orthologous variants: 93596158-T-C

79295071-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: 93591578-C-G

79295122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: 93591537-T-C

http://identifiers.org/hco/5/GRCh38#79300099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#93590644-C-A

79300099-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: 93590644-C-G

79300119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron variant
orthologous variants: 93590624-G-A

79300188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: synonymous variant
orthologous variants: 93590564-A-G

79300189-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: missense variant
orthologous variants: 93590563-C-G

79300189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: stop gained
orthologous variants: 93590563-C-T

79300201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: synonymous variant
orthologous variants: 93590551-T-C

79300303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 93590449-A-G

79300343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93590409-A-G

79300410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93590339-T-C

79300413-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93590336-A-T

http://identifiers.org/hco/5/GRCh38#79300783-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#93589974-A-C

http://identifiers.org/hco/5/GRCh38#79300932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#93589824-C-A

79300932-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93589824-C-G

79300932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93589824-C-T

http://identifiers.org/hco/5/GRCh38#79301003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#93589741-C-A

79301003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93589741-C-T

http://identifiers.org/hco/5/GRCh38#79301015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#93589729-C-A

79301015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93589729-C-T

http://identifiers.org/hco/5/GRCh38#79306330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#93589432-C-A

79306413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 93589361-G-A

79309303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93586887-A-G

79312262-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93579334-T-G

http://identifiers.org/hco/5/GRCh38#79312264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#93579332-C-A

79312264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93579332-C-T

79312317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93579280-A-G

http://identifiers.org/hco/5/GRCh38#79312522-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#93579061-A-C

79312522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93579061-A-G

79312522-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93579061-A-T

79312526-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93579057-T-A

79312526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93579057-T-C

79312526-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93579057-T-G

79314215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93578162-T-C

79314215-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93578162-T-G

79314227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93578149-A-G

79314238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93578143-A-G

79314316-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 93578068-A-T

79314421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 93577966-G-T

http://identifiers.org/hco/5/GRCh38#79314497-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#93577890-A-C

79314497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 93577890-A-G

http://identifiers.org/hco/5/GRCh38#79314647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#93577734-C-A

79314647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 93577734-C-T

http://identifiers.org/hco/5/GRCh38#79314650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#93577731-C-A

79314650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 93577731-C-T

http://identifiers.org/hco/5/GRCh38#79314812-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#93577560-A-C

http://identifiers.org/hco/5/GRCh38#79314858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#93577514-C-A

79314858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 93577514-C-T

79314880-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93577494-T-G

79314911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93577462-A-G

79315276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93577296-T-C

79315276-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93577296-T-G

79315330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93577252-A-G

79315469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93577176-G-A

79315563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93577095-G-T

79315962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93576289-G-A

79315962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93576289-G-T

79315976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93576279-A-G

79316176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 93576079-T-C

79316299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 93575956-G-A

http://identifiers.org/hco/5/GRCh38#79316349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#93575906-C-A

79316349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93575906-C-T

79316360-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93575895-T-A

79316360-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93575895-T-G

79316397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93575860-G-A

79316398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93575859-A-G

http://identifiers.org/hco/5/GRCh38#79316406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#93575852-C-A

79316406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93575852-C-T

79316425-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93575833-T-A

79317140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93575179-A-G

79317349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93575000-C-T

79318463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93574218-C-T

79318720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93574016-G-A

http://identifiers.org/hco/5/GRCh38#79318723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#93574013-C-A

79318800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93573947-A-G

79318800-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93573947-A-T

http://identifiers.org/hco/5/GRCh38#79318810-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#93573934-A-C

79318858-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93573888-C-G

79319139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93573680-A-G

79319175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93573648-G-A

79319196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93573630-G-A

http://identifiers.org/hco/5/GRCh38#79319198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#93573628-C-A

79321701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93571826-G-T

http://identifiers.org/hco/5/GRCh38#79321808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#93571742-C-A

http://identifiers.org/hco/5/GRCh38#79321816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#93571734-C-A

79322016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93571553-T-C

79322028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93571537-G-T

79322106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93571461-T-C

http://identifiers.org/hco/5/GRCh38#79322330-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#93571241-A-C

79322478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93571091-A-G

http://identifiers.org/hco/5/GRCh38#79322539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#93571038-C-A

79322542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93571035-C-T

79322641-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93570918-A-T

79322689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93570871-G-A

79322689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93570871-G-T

79322735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93570834-T-C

79322774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93570797-T-C

79322942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93570645-C-T

79322948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93570639-A-G

79322948-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93570639-A-T

79322961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93570628-T-C

79322969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93570620-G-T

79323002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93570596-A-G

79323584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93570233-G-A

79324208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93569450-G-T

79324333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93569294-C-T

79324523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93569178-C-T

79324554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93569143-C-T

http://identifiers.org/hco/5/GRCh38#79324569-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#93569128-A-C

http://identifiers.org/hco/5/GRCh38#79324575-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#93569115-A-C

79324626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93569066-G-T

79324635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93569058-A-G

79324967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93568637-A-G

http://identifiers.org/hco/5/GRCh38#79324997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#93568609-C-A

79324997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93568609-C-T

http://identifiers.org/hco/5/GRCh38#79325006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#93568600-C-A

79325006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93568600-C-T

http://identifiers.org/hco/5/GRCh38#79325054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#93568561-C-A

79325107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93568519-A-G

http://identifiers.org/hco/5/GRCh38#79325434-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#93568252-A-C

79325434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93568252-A-G

79325665-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93568063-G-C

http://identifiers.org/hco/5/GRCh38#79325709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#93568035-C-A

79325709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93568035-C-T

79325884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93567860-G-A

79326059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93567692-G-A

79326198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93567559-T-C

79326455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93567331-C-T

79326490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93567279-G-T

79326567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93567213-C-T

79326579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93567201-T-C

http://identifiers.org/hco/5/GRCh38#79326624-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#93567156-A-C

79326624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93567156-A-G

79326701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93567078-T-C

http://identifiers.org/hco/5/GRCh38#79326830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#93566964-C-A

79326852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93566944-G-A

79326977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28916
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93566822-C-T