180300833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: 3 prime UTR variant
orthologous variants: 49729308-G-T

180300835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: 3 prime UTR variant
orthologous variants: 49729306-G-A

180300905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: 3 prime UTR variant
orthologous variants: 49729235-G-A

180300905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: 3 prime UTR variant
orthologous variants: 49729235-G-T

180300959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: 3 prime UTR variant
orthologous variants: 49729187-G-A

180300959-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: 3 prime UTR variant
orthologous variants: 49729187-G-T

180300974-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: 3 prime UTR variant
orthologous variants: 49729172-A-T

180300984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: 3 prime UTR variant
orthologous variants: 49729162-G-A

180300984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: 3 prime UTR variant
orthologous variants: 49729162-G-T

180300986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: 3 prime UTR variant
orthologous variants: 49729160-A-G

180300986-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: 3 prime UTR variant
orthologous variants: 49729160-A-T

180301031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: 3 prime UTR variant
orthologous variants: 49729115-T-C

180301134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: 3 prime UTR variant
orthologous variants: 49729014-G-A

http://identifiers.org/hco/5/GRCh38#180301405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49728752-C-A

http://identifiers.org/hco/5/GRCh38#180301487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49728670-C-A

http://identifiers.org/hco/5/GRCh38#180302292-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49726779-A-C

180302292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49726779-A-G

180302295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49726776-A-G

180302295-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49726776-A-T

http://identifiers.org/hco/5/GRCh38#180302296-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49726775-A-C

180302314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49726749-A-G

180302314-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49726749-A-T

180302320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49726719-A-G

180302320-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49726719-A-T

180302475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: missense variant
orthologous variants: 49726546-A-G

180302501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: synonymous variant
orthologous variants: 49726520-C-T

180302502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: missense variant
orthologous variants: 49726519-A-G

180302507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: synonymous variant
orthologous variants: 49726514-G-A

180302541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: missense variant
orthologous variants: 49726480-G-A

http://identifiers.org/hco/5/GRCh38#180302591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49726430-C-A

180302600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49726421-A-G

http://identifiers.org/hco/5/GRCh38#180302610-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49726411-A-C

180302614-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49726407-G-C

180302614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49726407-G-T

180302674-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49726347-T-A

http://identifiers.org/hco/5/GRCh38#180302688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49726333-C-A

180302718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49726311-G-T

180303576-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49725525-A-T

180303617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49725483-G-A

180304040-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49724892-A-T

180304145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49724630-T-C

180304177-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49724610-T-A

180304395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49724409-A-G

180304412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49724392-A-G

180304455-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49724349-T-G

180304530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49724274-C-T

http://identifiers.org/hco/5/GRCh38#180304718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49723908-C-A

180304718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49723908-C-T

180304730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49723896-A-G

180304747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49723879-G-A

180304747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49723879-G-T

180304823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: synonymous variant
orthologous variants: 49723802-A-G

180304823-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: missense variant
orthologous variants: 49723802-A-T

180304848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: missense variant
orthologous variants: 49723777-G-A

180304862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: synonymous variant
orthologous variants: 49723763-A-G

180304893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: missense variant
orthologous variants: 49723732-C-T

180304895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: synonymous variant
orthologous variants: 49723730-A-G

180304895-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: synonymous variant
orthologous variants: 49723730-A-T

180304896-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: missense variant
orthologous variants: 49723729-G-C

180304903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: missense variant
orthologous variants: 49723722-T-C

180304913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: synonymous variant
orthologous variants: 49723712-G-A

180304920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: missense variant
orthologous variants: 49723705-T-C

180304920-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: missense variant
orthologous variants: 49723705-T-G

http://identifiers.org/hco/5/GRCh38#180304926-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49723699-A-C

180305054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49723563-G-A

180305054-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49723563-G-C

180305054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49723563-G-T

180305131-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49723485-C-G

180305292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49723350-C-T

180305327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49723315-C-T

180305399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49723219-C-T

180305478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49723143-C-T

180305558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49723061-T-C

180306426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49721699-C-T

180306481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49721647-T-C

180306943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49720945-C-T

http://identifiers.org/hco/5/GRCh38#180307066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49720835-C-A

180307294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: missense variant
orthologous variants: 49720574-T-C

http://identifiers.org/hco/5/GRCh38#180307362-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49720508-C-A

180307840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49720031-T-C

180307843-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49720028-T-A

180307846-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49720025-C-G

180312212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49718317-A-G

180312257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49718275-C-T

180312305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49718197-G-A

180312305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49718197-G-T

180312312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49718192-G-A

180312312-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49718192-G-C

180313611-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49717886-T-A

http://identifiers.org/hco/5/GRCh38#180313708-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49717795-A-C

180313708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49717795-A-G

http://identifiers.org/hco/5/GRCh38#180313711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49717792-C-A

180313711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49717792-C-T

180313829-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: missense variant
orthologous variants: 49717704-T-A

180313850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: missense variant
orthologous variants: 49717683-A-G

180313859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: missense variant
orthologous variants: 49717674-T-C

180313989-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49717543-G-C

180313989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49717543-G-T

http://identifiers.org/hco/5/GRCh38#180313990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49717542-C-A

180313990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49717542-C-T

180314034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49717496-T-C

http://identifiers.org/hco/5/GRCh38#180314108-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49717431-C-A

180314108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49717431-C-T

http://identifiers.org/hco/5/GRCh38#180314191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49717336-C-A

http://identifiers.org/hco/5/GRCh38#180314192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49717335-C-A

180314196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49717331-G-A

180314589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49716979-C-T

180314624-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49716965-T-A

180314655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49716932-G-A

180314655-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49716932-G-C

180314758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49716834-G-T

180314790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49716801-C-T

180315640-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49716131-T-G

180315886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, undefined
orthologous variants: 49715903-A-G

180316091-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, undefined
orthologous variants: 49715626-G-C

180316243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49715386-A-G

180316273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49715356-G-A

180316273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49715356-G-T

180316325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49715293-T-C

180316332-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49715286-G-C

180316400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: missense variant
orthologous variants: 49715218-A-G

http://identifiers.org/hco/5/GRCh38#180316623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#49715005-C-A

180316623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, undefined
orthologous variants: 49715005-C-T

http://identifiers.org/hco/5/GRCh38#180316652-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49714977-A-C

180316652-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49714977-A-T

180316716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49714922-T-C

180316732-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, undefined
orthologous variants: 49714906-T-G

180316749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, undefined
orthologous variants: 49714878-A-G

180316828-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49714799-T-G

180316865-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 49714762-C-G

180316894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49714724-G-T

180316946-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49714671-C-G

180316946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49714671-C-T

http://identifiers.org/hco/5/GRCh38#180316995-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49714622-A-C

180317043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49714574-A-G

180317046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49714571-G-A

180317046-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49714571-G-C

180317046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49714571-G-T

http://identifiers.org/hco/5/GRCh38#180317125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49714435-C-A

180317125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49714435-C-T

180317142-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49714418-A-T

180317144-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49714416-G-C

180317144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49714416-G-T

http://identifiers.org/hco/5/GRCh38#180317181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49714374-C-A

180317265-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49714287-G-C

180318746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49714265-G-A

180318746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49714265-G-T

http://identifiers.org/hco/5/GRCh38#180318755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49714256-C-A

180318755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49714256-C-T

180318766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49714228-C-T

180318850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49714143-C-T

180319091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49714007-T-C

http://identifiers.org/hco/5/GRCh38#180319099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49713999-C-A

180319099-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49713999-C-G

180319099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49713999-C-T

180319632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49713631-A-G

180319650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49713613-C-T

180322190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49711124-G-A

180322566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49710735-G-A

http://identifiers.org/hco/5/GRCh38#180324437-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49709840-A-C

180324437-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49709840-A-T

180324706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49709589-G-A

180324706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49709589-G-T

180324778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49709518-A-G

180324790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49709506-G-A

180324790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49709506-G-T

180325070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49709226-G-A

180325148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49709142-G-A

180325154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49709140-C-T

180325182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49709112-A-G

180325205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49709089-G-A

180325427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49708892-C-T

180325597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49708141-C-T

180325722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49708034-G-A

180326161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49707928-G-T

180326174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49707915-G-A

180327006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49706405-G-A

180328283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49706160-G-T

180328372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49706065-T-C

180328434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49706001-G-T

http://identifiers.org/hco/5/GRCh38#180328454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49705976-C-A

180328608-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49705833-T-A

180328624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49705819-G-A

180329104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49705069-C-T

180329135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49705038-T-C

180329188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 49704985-C-T

180329207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49704966-C-T

180329226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49704947-G-A

180329315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49704856-G-T

180329567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49703697-A-G

180329574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49703690-C-T

180329578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49703686-C-T

180329715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49703559-G-A

180329741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49703525-G-A

180329987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49703260-C-T

180330486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49702783-C-T

180330785-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49702544-G-C

180330835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: non_coding_transcript_exon_variant, splice_acceptor_variant, undefined
orthologous variants: 49702494-C-T

180330843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 49702486-T-C

180330843-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 49702486-T-G

180330851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 49702477-G-T

180330890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 49702436-G-T

http://identifiers.org/hco/5/GRCh38#180330909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#49702417-C-A

180331168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, undefined
orthologous variants: 49702177-T-C

180331295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49702048-A-G

180331323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron variant
orthologous variants: 49702021-T-C

http://identifiers.org/hco/5/GRCh38#180331371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#49701973-C-A

180331371-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, undefined
orthologous variants: 49701973-C-G

180331371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, undefined
orthologous variants: 49701973-C-T

180331377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, undefined
orthologous variants: 49701967-T-C

http://identifiers.org/hco/5/GRCh38#180331415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#49701929-C-A

180331445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49701900-G-T

180335637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49700167-T-C

180335807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49700000-A-G

180336249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49698892-T-C

http://identifiers.org/hco/5/GRCh38#180336333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49698819-C-A

180336333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49698819-C-T

180336344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49698808-C-T

http://identifiers.org/hco/5/GRCh38#180336439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49698711-C-A

180336439-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49698711-C-G

180336439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49698711-C-T

180336445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49698705-A-G

180336562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49698535-C-T

180336574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49698523-A-G

180336584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 49698513-T-C

180338350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49696235-A-G

180338350-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49696235-A-T

180338372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49695985-A-G

180338379-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49695977-T-G

180338445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49695909-G-A

180338445-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49695909-G-C

180338445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49695909-G-T

http://identifiers.org/hco/5/GRCh38#180338446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49695908-C-A

180338446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49695908-C-T

180338450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49695904-G-A

180338450-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49695904-G-C

180338450-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49695904-G-T

180338475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49695903-G-A

180338475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49695903-G-T

http://identifiers.org/hco/5/GRCh38#180338492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49695885-C-A

180338492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 49695885-C-T

180338509-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49695868-T-A

180338561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49695816-C-T

180338621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49695755-G-T

180338624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49695752-G-T

180338704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49695642-A-G

180338710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49695636-T-C

180338735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49695611-T-C

180343256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49692700-G-A

180343275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49692679-C-T

180343332-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49692638-C-G

180343332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49692638-C-T

180343481-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49692477-T-G

http://identifiers.org/hco/5/GRCh38#180343485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49692473-C-A

180343485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49692473-C-T

180343616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49692351-T-C

180343768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49692207-T-C

180343963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49692029-T-C

180344377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49691402-C-T

180344385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49691394-C-T

http://identifiers.org/hco/5/GRCh38#180344856-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49690947-A-C

180344856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49690947-A-G

180344983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49690835-G-A

180345020-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49690783-A-T

180345138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49690621-G-T

180345359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49690362-T-C

180345361-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49690360-G-C

180345464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49690237-G-A

180345512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49690194-G-A

180345512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49690194-G-T

180345644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49690046-T-C

180345775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49689910-G-A

180345812-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49689866-G-C

180347642-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49689778-T-A

180347642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49689778-T-C

180347642-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49689778-T-G

180347656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49689774-G-A

http://identifiers.org/hco/5/GRCh38#180347718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49689714-C-A

180347718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49689714-C-T

180347831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49689637-G-A

180350938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49686975-C-T

180351845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49686354-C-T

180351847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49686352-G-A

180352051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49686155-G-T

180352226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49685979-G-A

180352226-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49685979-G-C

180352226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49685979-G-T

http://identifiers.org/hco/5/GRCh38#180352269-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49685933-A-C

http://identifiers.org/hco/5/GRCh38#180352302-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49685900-A-C

http://identifiers.org/hco/5/GRCh38#180352683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49685515-C-A

180352683-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 49685515-C-G

180352783-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 49685413-T-A

180352783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 49685413-T-C

180352783-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 49685413-T-G

http://identifiers.org/hco/5/GRCh38#180352795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49685401-C-A

180352795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 49685401-C-T

180352914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49685296-G-A

180352914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49685296-G-T

http://identifiers.org/hco/5/GRCh38#180352951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49685259-C-A

180352951-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49685259-C-G

180352951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49685259-C-T

180352988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49685235-G-A

180352988-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49685235-G-T

180353104-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49685134-C-G

180353104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49685134-C-T

180353187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49685082-G-A

180353187-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49685082-G-C

180353187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49685082-G-T

http://identifiers.org/hco/5/GRCh38#180353201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49685078-C-A

180353201-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49685078-C-G

180353201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49685078-C-T

180353277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 49685033-G-A

180353277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4242
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 49685033-G-T