127707807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3 prime UTR variant
orthologous variants: 28760538-T-C

127708010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3 prime UTR variant
orthologous variants: 28758960-C-T

http://identifiers.org/hco/6/GRCh38#127708012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28758958-C-A

127708120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3 prime UTR variant
orthologous variants: 28758855-C-T

127708275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3 prime UTR variant
orthologous variants: 28758702-A-G

127708477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3 prime UTR variant
orthologous variants: 28758495-G-T

127708516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3 prime UTR variant
orthologous variants: 28758464-A-G

127708646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3 prime UTR variant
orthologous variants: 28758323-A-G

http://identifiers.org/hco/6/GRCh38#127708729-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28758215-C-A

127708729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3 prime UTR variant
orthologous variants: 28758215-C-T

127708931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3 prime UTR variant
orthologous variants: 28758022-G-A

127708931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3 prime UTR variant
orthologous variants: 28758022-G-T

127709021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3 prime UTR variant
orthologous variants: 28757929-A-G

127709021-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3 prime UTR variant
orthologous variants: 28757929-A-T

127709094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3 prime UTR variant
orthologous variants: 28757862-A-G

127709126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3 prime UTR variant
orthologous variants: 28757833-G-A

127709157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3 prime UTR variant
orthologous variants: 28757803-G-A

127709157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3 prime UTR variant
orthologous variants: 28757803-G-T

http://identifiers.org/hco/6/GRCh38#127709298-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28757660-A-C

127709298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3 prime UTR variant
orthologous variants: 28757660-A-G

http://identifiers.org/hco/6/GRCh38#127709319-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28757639-A-C

127709472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3 prime UTR variant
orthologous variants: 28757490-A-G

127709556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3 prime UTR variant
orthologous variants: 28757406-G-T

127709578-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3 prime UTR variant
orthologous variants: 28757383-T-A

127709578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3 prime UTR variant
orthologous variants: 28757383-T-C

127709700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3 prime UTR variant
orthologous variants: 28757260-A-G

127709882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3 prime UTR variant
orthologous variants: 28757080-T-C

127709882-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3 prime UTR variant
orthologous variants: 28757080-T-G

127709891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3 prime UTR variant
orthologous variants: 28757071-C-T

127709934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3 prime UTR variant
orthologous variants: 28757027-T-C

127709975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3 prime UTR variant
orthologous variants: 28756986-T-C

127709977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3 prime UTR variant
orthologous variants: 28756984-A-G

127709977-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3 prime UTR variant
orthologous variants: 28756984-A-T

127709987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: undefined
orthologous variants: 28756974-A-G

127710014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 28756947-T-C

http://identifiers.org/hco/6/GRCh38#127710094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28756882-C-A

127710094-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28756882-C-G

127710094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28756882-C-T

http://identifiers.org/hco/6/GRCh38#127710107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28756865-C-A

http://identifiers.org/hco/6/GRCh38#127710144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28756829-C-A

127710144-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28756829-C-G

127710247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28756757-T-C

127710330-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28756674-T-G

127710618-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28756444-T-G

127711643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28754207-T-C

http://identifiers.org/hco/6/GRCh38#127711698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28754167-C-A

127711809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28754059-G-A

127711809-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28754059-G-C

127711809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28754059-G-T

127711840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28754030-T-C

127711967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28753907-A-G

127712140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28753737-C-T

127712202-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28753675-T-A

127712203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28753674-G-A

127712263-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28753615-T-G

127712272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28753606-A-G

127712416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28753491-C-T

127712417-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28753490-A-T

127712488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28753416-A-G

127712523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28753378-C-T

127712651-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28753241-T-A

127712784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28753119-T-C

127712817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28753074-A-G

127713205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28752662-G-A

127713229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28752640-T-C

127713429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28752436-G-A

127713522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28752337-A-G

127713704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28752160-A-G

127713767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28752131-A-G

127713885-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28752020-G-C

127713885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28752020-G-T

127713946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28751957-A-G

127714023-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28751803-T-G

127714024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28751802-G-A

127714140-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28751689-A-T

127714196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28751603-T-C

127714694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28751007-T-C

127714794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28750905-C-T

127714991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28750708-G-A

127714991-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28750708-G-C

127715174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28750537-G-A

127715279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28750372-G-A

127715348-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28750166-C-G

127715351-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28750163-T-G

127715559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28749944-A-G

127715779-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28749705-A-T

127715807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28749677-A-G

127715822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28749664-G-A

127715940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28749563-G-T

127715955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28749547-C-T

127716027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28749478-A-G

127716147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28749361-G-A

127716294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28749256-A-G

127716456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28749093-C-T

127716576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28748999-T-C

127716632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28748944-G-A

127716645-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28748931-T-A

127716692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28748884-G-A

127717004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28748650-A-G

127717124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28748558-T-C

127717405-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28748300-T-A

127717405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28748300-T-C

127717610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28748108-C-T

127717613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28748105-G-A

127717638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28748075-T-C

127717745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28747993-T-C

http://identifiers.org/hco/6/GRCh38#127718094-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28747497-A-C

127718163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28747424-C-T

127718500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28747101-A-G

http://identifiers.org/hco/6/GRCh38#127718643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28746963-C-A

127718773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28746834-T-C

127719303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28746308-A-G

127719595-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28739526-A-T

127719602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28739519-A-G

http://identifiers.org/hco/6/GRCh38#127719614-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28739507-A-C

http://identifiers.org/hco/6/GRCh38#127719616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28739505-C-A

http://identifiers.org/hco/6/GRCh38#127719628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28739493-C-A

127719628-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28739493-C-G

127719628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28739493-C-T

http://identifiers.org/hco/6/GRCh38#127719677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28739439-C-A

http://identifiers.org/hco/6/GRCh38#127719721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: stop gained
orthologous variants: http://identifiers.org/mco/10/GRCm39#28739396-C-A

127719721-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: missense variant
orthologous variants: 28739396-C-G

127719791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: synonymous variant
orthologous variants: 28739326-G-A

127719791-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: missense variant
orthologous variants: 28739326-G-C

http://identifiers.org/hco/6/GRCh38#127719813-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28739304-A-C

127719903-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28739213-A-T

127720024-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28739098-G-C

127720130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28738993-A-G

127720161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28738962-C-T

127720170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28738953-A-G

127720225-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28738718-T-A

127720259-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28738648-A-T

127720275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28738632-A-G

127720553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28738359-T-C

127720612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28738302-G-A

127720683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28738231-T-C

127721092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28737731-C-T

http://identifiers.org/hco/6/GRCh38#127721497-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28737355-A-C

127722339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28736292-T-C

127722445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28736182-C-T

127722490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28736141-C-T

127722610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28736032-C-T

127722674-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28735980-G-C

127722750-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28735940-C-G

http://identifiers.org/hco/6/GRCh38#127724192-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28735724-A-C

127724513-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28735417-T-G

127724557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28735379-A-G

127724558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28735378-T-C

127724702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28735256-T-C

127725303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28734736-A-G

127725342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28734705-T-C

127725382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28734693-T-C

127725815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28734305-G-A

127725815-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28734305-G-C

127725851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28734270-C-T

127725880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28734242-A-G

127725930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28734197-T-C

127726340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28733860-A-G

127726375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28733825-T-C

127726381-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28733819-T-G

127726406-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28733788-T-A

http://identifiers.org/hco/6/GRCh38#127727014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28733453-C-A

127727037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28733430-A-G

127727257-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28732830-T-A

127727268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28732819-A-G

http://identifiers.org/hco/6/GRCh38#127727466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28732639-C-A

127727536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28732573-T-C

127727698-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28732419-T-G

http://identifiers.org/hco/6/GRCh38#127727710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28732407-C-A

127735435-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28724873-C-G

127735534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28724638-T-C

127735776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28724395-C-T

127736127-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28723346-C-G

127736148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28723325-A-G

127736213-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28723241-T-A

127736214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28723240-G-T

127736237-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28723223-T-A

127736237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28723223-T-C

127736476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28723016-T-C

127736499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28722811-G-A

http://identifiers.org/hco/6/GRCh38#127736631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28722684-C-A

127736751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28722571-C-T

127736790-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28722528-T-A

127736796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28722522-G-A

http://identifiers.org/hco/6/GRCh38#127736842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28722472-C-A

127737170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28720308-C-T

127737191-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28720287-T-G

127737268-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28720210-A-T

127737342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28720032-A-G

127737605-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28719764-A-T

127737658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28719706-C-T

127737955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28719394-G-A

127738110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28719272-T-C

127738389-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28718986-T-A

127738566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28718832-C-T

127738589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28718809-C-T

127738787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28718607-A-G

127738938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28718490-C-T

127739366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28718099-G-A

127740046-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28717211-A-T

127740092-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28717181-T-G

127740294-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28716959-G-C

127740294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28716959-G-T

127741164-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28716100-A-T

127741202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28716085-G-A

127741202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28716085-G-T

127741301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28715987-A-G

127742643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28714657-A-G

127742935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28714370-T-C

http://identifiers.org/hco/6/GRCh38#127743153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28714159-C-A

127743202-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28714111-T-A

127743241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28714072-C-T

127743301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28714006-C-T

127743679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28713634-T-C

127743810-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28713493-T-A

127743923-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28713363-T-A

127743944-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28713341-T-A

127744051-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28713236-G-C

127744378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28712947-C-T

127744482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28712874-A-G

127744491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28712865-C-T

127744509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28712848-A-G

127744852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28712410-C-T

127744918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28712319-T-C

127745174-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28711885-T-A

127745275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28711789-C-T

http://identifiers.org/hco/6/GRCh38#127745421-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28711574-A-C

127745537-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28711459-T-A

127745560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28711436-A-G

http://identifiers.org/hco/6/GRCh38#127745599-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28711397-C-A

127745623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28711368-T-C

127745644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28711348-G-A

http://identifiers.org/hco/6/GRCh38#127745785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28711315-C-A

127746081-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28711031-T-A

127748855-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28710133-G-C

http://identifiers.org/hco/6/GRCh38#127748862-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28710117-A-C

127748988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28709975-A-G

127749074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28709894-T-C

127749170-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28709796-C-G

127749361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28709606-C-T

127749380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28709587-G-A

127749597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28707479-T-C

127749664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28707415-T-C

127749716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28707364-T-C

127750048-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28706745-C-G

127750142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28706660-G-T

127750287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28703651-T-C

127750448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28703499-G-A

127750581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28703146-C-T

127750606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28703121-T-C

http://identifiers.org/hco/6/GRCh38#127750904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28702752-C-A

127751001-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28702667-T-A

127751045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28702647-T-C

127751064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28702642-A-G

127751124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28702583-A-G

127751133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28702574-G-A

127751263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28702450-C-T

127751429-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28702294-C-G

127751649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28702075-C-T

http://identifiers.org/hco/6/GRCh38#127755324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28699189-C-A

127755369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28699149-A-G

127755484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28699043-C-T

127755595-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28698941-G-C

127755706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28698760-T-C

127756020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28698407-C-T

127756234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28698216-T-C

127756362-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28698099-T-A

127756362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28698099-T-C

127756440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28698022-T-C

127756639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28697816-G-A

127756661-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28697793-T-A

127756666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28697788-T-C

127756775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28697680-A-G

http://identifiers.org/hco/6/GRCh38#127756809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28697646-C-A

127756896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28697551-A-G

127756896-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28697551-A-T

127763415-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28697071-T-A

127763418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28697066-A-G

127763615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28696883-G-A

http://identifiers.org/hco/6/GRCh38#127763654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28696836-C-A

127763671-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28696806-C-G

http://identifiers.org/hco/6/GRCh38#127763687-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28696788-A-C

127763966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28696677-C-T

127763990-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28696652-T-A

127764298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28695177-A-G

127764298-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28695177-A-T

127764463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28695055-G-T

127764527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28694992-G-A

127764527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28694992-G-T

127764593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28694934-T-C

127764611-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28694916-C-G

127764709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28694822-C-T

127764923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28694692-A-G

127765303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28693965-G-A

127765341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28693928-G-A

127765369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28693900-T-C

127765388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28693882-G-A

http://identifiers.org/hco/6/GRCh38#127765467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28693819-C-A

127765512-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28693774-T-A

127765931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28693686-G-A

127765941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28693676-A-G

127765941-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28693676-A-T

127765978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28693634-T-C

127765983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28693629-T-C

127766031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28693582-T-C

127766090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28693409-T-C

127768047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28692265-G-T

127768048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28692264-C-T

127768144-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28692173-C-G

http://identifiers.org/hco/6/GRCh38#127768178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28692138-C-A

127768219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28692108-A-G

127768224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28692103-G-A

127768290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28692039-C-T

http://identifiers.org/hco/6/GRCh38#127768346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28691983-C-A

127768694-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28691638-T-A

127768706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28691626-G-A

127768706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28691626-G-T

127768870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28691489-C-T

http://identifiers.org/hco/6/GRCh38#127768956-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28691403-A-C

127769018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28691342-A-G

127769029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28691332-C-T

127769138-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28691223-T-G

127769320-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28691038-G-C

127769380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28690994-C-T

127769383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28690991-G-T

127769436-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28690940-T-A

127769455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28690925-C-T

127771762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28690473-C-T

127771822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28690196-A-G

127771987-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28690019-T-G

127772015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28689990-A-G

127772239-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28689776-T-A

127772324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28689690-C-T

127772467-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28689537-T-A

127772486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28689510-A-G

127772530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28689456-G-T

127772667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28689314-C-T

127772688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28689299-G-A

127772691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28689296-T-C

127772705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28689282-T-C

127773015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28688974-C-T

127773016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28688973-G-A

127773016-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28688973-G-C

127773016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28688973-G-T

127773198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28688788-T-C

http://identifiers.org/hco/6/GRCh38#127773268-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28688710-C-A

127773411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28688585-T-C

127773482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28688519-T-C

127773870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28688147-T-C

127773935-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28688086-C-G

127773935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28688086-C-T

127774040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28687991-A-G

127774698-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28687347-T-A

127774698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28687347-T-C

127774699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28687346-G-A

127776874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28685035-T-C

127777071-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28684807-A-T

127777151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28684732-G-A

127777188-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28684698-G-C

127777188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28684698-G-T

127777256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28684641-T-C

127777316-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28684582-T-G

127777895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28683694-G-A

127777895-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28683694-G-T

127777900-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28683689-A-T

127777936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28683648-T-C

127777962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28683622-T-C

127778423-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28683236-A-T

127778536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28683139-G-A

127778687-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28682988-A-T

127778803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28682874-G-T

127778868-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28682810-T-G

http://identifiers.org/hco/6/GRCh38#127778872-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28682806-A-C

127778872-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28682806-A-T

127779291-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28681081-G-C

127779471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28680902-T-C

http://identifiers.org/hco/6/GRCh38#127779752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28680627-C-A

127779878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28680510-T-C

127779899-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28680489-G-C

127785898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28679777-T-C

127785898-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28679777-T-G

127786020-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28679662-T-A

127786020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28679662-T-C

127786312-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28679277-T-G

127786440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28679175-G-A

127788569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28676698-A-G

127788596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28676671-T-C

127788627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28676639-C-T

127788634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28676632-G-A

127792778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28674704-C-T

127793220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28674253-G-A

127793241-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28674232-G-C

127793269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28674194-G-T

127793417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28674062-G-A

127793774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28673448-G-T

http://identifiers.org/hco/6/GRCh38#127793884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28673300-C-A

127793884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28673300-C-T

127793891-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28673293-C-G

127793891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28673293-C-T

127794115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28673076-T-C

127794187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28673005-A-G

127794449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28672752-C-T

127796196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28672308-G-A

127796282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28672229-T-C

127796299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28672215-T-C

127796402-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28672116-A-T

127796407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28672113-G-A

127796407-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28672113-G-T

127796584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28671933-A-G

127796694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28671817-C-T

127796977-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28671265-C-G

127797170-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28671137-G-C

127797202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28671105-G-T

127797203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28671104-A-G

127797273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28671036-T-C

127797325-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28670990-A-T

127797513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28670804-G-A

127797621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28670712-G-T

127797853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28670475-C-T

127797895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28670442-A-G

127797974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28670372-G-T

127798080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28670287-A-G

127798187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28670181-C-T

127799145-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28668461-G-C

127799620-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28667161-A-T

127799638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28667143-T-C

127807991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28666416-G-T

127807995-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28666412-T-G

127808025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28666382-A-G

127808029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28666378-C-T

127808169-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28666240-C-G

127808169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28666240-C-T

127808497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28665913-A-G

127808499-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28665911-A-T

127808812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28665671-T-C

127808917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28665570-A-G

127808918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28665569-C-T

127808919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28665568-C-T

127808920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28665567-G-A

127808983-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28665504-T-G

127808986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28665501-C-T

127809006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28665480-T-C

127809459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28665023-T-C

127809462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28665020-T-C

127809506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28664976-G-A

127809531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28664952-G-A

127809738-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28664762-G-C

127809738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28664762-G-T

http://identifiers.org/hco/6/GRCh38#127809879-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28664476-A-C

127809944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28664418-A-G

127809985-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28664376-G-C

127809990-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28664371-C-G

127809990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28664371-C-T

127810039-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28664333-T-A

127810041-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28664331-A-T

127810044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28664326-A-G

127810102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28664286-T-C

127810154-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28664236-A-T

127810198-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28664210-A-T

127810268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28664138-T-C

127812172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28659436-G-A

127812630-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28658987-T-G

127812682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28658936-A-G

127812744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28658862-T-C

http://identifiers.org/hco/6/GRCh38#127812798-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28658811-A-C

127812798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28658811-A-G

127812798-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28658811-A-T

127812803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28658806-A-G

http://identifiers.org/hco/6/GRCh38#127812877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28658742-C-A

127812877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28658742-C-T

127812935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: missense variant
orthologous variants: 28658684-G-T

127812944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: missense variant
orthologous variants: 28658675-G-A

127812952-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: synonymous variant
orthologous variants: 28658667-T-A

127813052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: missense variant
orthologous variants: 28658567-G-T

127813055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: missense variant
orthologous variants: 28658564-C-T

127813172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: missense variant
orthologous variants: 28658441-A-G

127813495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: synonymous variant
orthologous variants: 28658121-G-A

127813495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: synonymous variant
orthologous variants: 28658121-G-T

http://identifiers.org/hco/6/GRCh38#127813502-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28658114-A-C

127813754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: missense variant
orthologous variants: 28657862-A-G

127813769-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: missense variant
orthologous variants: 28657847-G-C

127813769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: missense variant
orthologous variants: 28657847-G-T

127814002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28657603-T-C

127814002-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28657603-T-G

127814066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28657536-G-A

127814066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28657536-G-T

127814078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28657524-T-C

127814233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28657379-T-C

127814487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28657126-A-G

127814492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28657112-C-T

127814519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28657091-T-C

127814706-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28656897-T-G

127814718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28656886-A-G

127815463-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28656290-C-G

127815463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28656290-C-T

127815548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28656204-T-C

127815740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28656004-T-C

127815847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28655891-T-C

127816080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28655067-C-T

127816236-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28654933-A-T

127816331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28654828-T-C

127817092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28654050-T-C

127817191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28653904-G-A

127817312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28653792-T-C

127817344-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28653762-A-T

http://identifiers.org/hco/6/GRCh38#127817405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28653725-C-A

127817715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28653474-G-A

127817750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28653433-G-A

127818028-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28653178-T-G

127818120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28653076-A-G

127818120-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28653076-A-T

127818347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28652863-T-C

127821002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28651811-T-C

127821075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28651750-A-G

http://identifiers.org/hco/6/GRCh38#127821076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28651749-C-A

127821232-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28651511-G-C

127821248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28651496-C-T

127821731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28650945-T-C

127821784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28650887-A-G

127822325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28644451-A-G

127823950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28644123-A-G

127823988-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28644096-G-T

127824036-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28644044-G-C

127825287-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28641770-T-G

127825628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28641431-A-G

127826068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28641232-A-G

127826086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28641215-T-C

http://identifiers.org/hco/6/GRCh38#127826195-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28641094-A-C

127826195-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28641094-A-T

127826302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28640987-T-C

127826833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28640480-A-G

127826840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28640473-T-C

127826867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28640447-T-C

127826873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28640439-G-A

127827193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28639809-T-C

127827245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28639765-C-T

127827420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28639622-A-G

127827584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28639475-A-G

127827585-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28639474-T-G

127827631-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28639425-C-G

http://identifiers.org/hco/6/GRCh38#127827768-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28639309-A-C

127827924-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28639129-A-T

127827970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28639093-C-T

127828132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28638972-T-C

127828161-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28638943-T-A

127828338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28638766-A-G

127829348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28637734-G-A

127829348-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28637734-G-C

127829348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28637734-G-T

127829364-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28637718-G-T

http://identifiers.org/hco/6/GRCh38#127829401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28637683-C-A

127829401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28637683-C-T

http://identifiers.org/hco/6/GRCh38#127829424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28637659-C-A

127829424-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28637659-C-G

127829424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28637659-C-T

127829451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28637632-A-G

http://identifiers.org/hco/6/GRCh38#127829453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28637630-C-A

127829453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28637630-C-T

127829565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron_variant, missense_variant
orthologous variants: 28637518-T-C

127829901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 28637182-T-C

127830071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28636724-T-C

127830384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28636416-G-T

127830901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28636242-A-G

127833372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28635123-A-G

127833604-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28634883-G-C

127834643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28632631-T-C

127834662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28632612-T-C

127834837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28632428-T-C

127835074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28632250-A-G

127835118-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28632232-G-C

http://identifiers.org/hco/6/GRCh38#127835368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28632047-C-A

127835420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28631999-T-C

127835650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28631806-A-G

127835884-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28631588-T-G

127836647-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28630821-T-A

127837203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28629711-T-C

127837255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28629660-A-G

127837333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28629605-G-A

http://identifiers.org/hco/6/GRCh38#127837557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28629439-C-A

127837779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28629230-T-C

127837779-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28629230-T-G

127838012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28629015-A-G

127838454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28628571-G-A

127838464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28628560-C-T

127838513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28628471-T-C

127838518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28628466-T-C

127840957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28617686-G-A

127840989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28617660-G-A

http://identifiers.org/hco/6/GRCh38#127840995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28617654-C-A

127841152-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28617503-C-G

127841174-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28617485-T-G

127841177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28617482-G-A

127841200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28617459-T-C

127841205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28617453-G-A

127841351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28617065-A-G

127841351-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28617065-A-T

127841403-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28617013-C-G

127841704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28616748-G-A

127841780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28616677-G-A

http://identifiers.org/hco/6/GRCh38#127841990-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28616478-A-C

127842021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 28616447-T-C

127844128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28614890-G-A

127844128-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28614890-G-T

127844173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28614852-G-A

127844173-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28614852-G-C

127844235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28614787-G-A

127844315-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28614737-T-G

127844316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28614736-G-A

http://identifiers.org/hco/6/GRCh38#127844368-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28614686-A-C

127844380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28614674-G-T

127844579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28614404-C-T

127844766-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28614217-T-G

127845017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28613961-A-G

127845286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28613701-G-A

127845286-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28613701-G-C

127845428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28613531-C-T

127845634-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28613373-A-T

127845697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28613286-T-C

127845749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28613236-C-T

127845758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28613227-G-A

127845835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28613155-T-C

http://identifiers.org/hco/6/GRCh38#127846046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28612970-C-A

127846053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28612963-G-A

127846197-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28612811-A-T

127846248-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28612766-C-G

127846248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28612766-C-T

127846275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28612742-T-C

127852679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28605156-A-G

127852727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28605115-C-T

http://identifiers.org/hco/6/GRCh38#127852765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28605077-C-A

127852777-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28605069-T-A

127852803-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28605058-T-G

127852805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28605056-T-C

127852928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28604946-A-G

127853069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28604811-A-G

127853072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28604808-T-C

127853132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28604768-G-A

127853221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28604682-T-C

127853301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28604339-G-A

127853301-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28604339-G-T

127853347-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28604294-C-G

127853504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28604153-G-A

127853542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28604122-T-C

http://identifiers.org/hco/6/GRCh38#127853601-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28604064-A-C

127853878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28603782-A-G

127853916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28603752-C-T

127853976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28603703-T-C

127853992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28603687-T-C

127854034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28603652-C-T

127854037-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28603649-C-G

127854096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28603599-T-C

127854197-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28603519-C-G

127854197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28603519-C-T

127854227-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28603488-T-G

127854305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28603412-T-C

http://identifiers.org/hco/6/GRCh38#127854386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#28603337-C-A

127854464-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28603268-A-T

127855055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 28598605-T-C

127855055-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 28598605-T-G

127855101-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 28598556-A-T

http://identifiers.org/hco/6/GRCh38#127855194-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28598463-A-C

127855194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 28598463-A-G

127855216-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28598449-T-A

127855216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28598449-T-C

127855217-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28598448-T-A

127855217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28598448-T-C

127855218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28598447-T-C

127855224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28598441-A-G

http://identifiers.org/hco/6/GRCh38#127855238-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28598424-A-C

127855238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28598424-A-G

127855238-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28598424-A-T

127855254-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28598408-A-T

127855340-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28598333-C-G

127855588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28598199-T-C

127855616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28598167-C-T

http://identifiers.org/hco/6/GRCh38#127855993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28597798-C-A

127856030-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28597762-C-G

127856030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28597762-C-T

127856134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28597656-A-G

127856169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28597622-T-C

127856392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28597404-G-A

127856412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28597387-C-T

127856420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28597379-G-T

127856521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28597169-A-G

127856664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28597072-A-G

127856664-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28597072-A-T

127856906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28596846-C-T

127856987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28596563-A-G

127856997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28596552-G-A

http://identifiers.org/hco/6/GRCh38#127857129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28596440-C-A

127857129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28596440-C-T

http://identifiers.org/hco/6/GRCh38#127857172-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28596389-C-A

127857207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28596354-G-A

127857218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28596343-G-A

127857610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28595958-A-G

127857845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28595722-T-C

127858204-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28595388-A-T

127858245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28595356-G-A

127858389-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28595199-G-C

127858763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28594536-G-A

http://identifiers.org/hco/6/GRCh38#127859488-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28593809-A-C

127859488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28593809-A-G

127859588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28593716-T-C

127859622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28593694-G-A

127859622-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28593694-G-C

127859622-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28593694-G-T

http://identifiers.org/hco/6/GRCh38#127859752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28593568-C-A

127859784-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28593529-T-G

127859892-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28593175-C-G

127860005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28593061-C-T

127860025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28593041-G-A

127860093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28592981-G-A

127860103-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28592971-A-T

127860236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28592841-G-A

127860382-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28590342-C-G

http://identifiers.org/hco/6/GRCh38#127860410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28590318-C-A

127860410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28590318-C-T

127860444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28590304-A-G

127860526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28590219-G-A

127860563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28590185-T-C

127860612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28590140-A-G

127860882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28583170-A-G

127861320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28582740-A-G

127861937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28582477-A-G

127862289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28582176-G-A

127862620-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28582021-T-A

127862940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28581858-C-T

127863099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28581705-T-C

127863272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28581554-C-T

127863481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28581346-G-A

http://identifiers.org/hco/6/GRCh38#127863491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28581336-C-A

127863491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28581336-C-T

127863689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28581153-T-C

127864294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28580084-G-A

127864294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28580084-G-T

127864320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28580058-T-C

127864371-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28579995-A-T

127864402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28579965-G-A

127864416-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28579948-T-A

127865838-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28579852-C-G

127865842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28579848-A-G

127865861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28579834-A-G

127866577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28579402-T-C

127866608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28579369-G-A

127867033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28575334-T-C

127867179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28575208-G-A

127867269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28575133-C-T

127867355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28574961-C-T

127867675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28574552-G-A

127867949-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28574281-T-G

127867995-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28574237-A-T

127876097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28569735-T-C

127876115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28569717-A-G

127876725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28568674-T-C

127876810-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28568589-A-T

127876815-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28568584-T-A

127878433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28565642-G-A

http://identifiers.org/hco/6/GRCh38#127878613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28565461-C-A

127878647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28565426-A-G

127878901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28565285-G-T

127879014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28565222-T-C

127879125-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28565141-T-A

http://identifiers.org/hco/6/GRCh38#127880621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28564040-C-A

http://identifiers.org/hco/6/GRCh38#127880967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28563753-C-A

127881027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28563696-T-C

127881444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28563358-T-C

127881729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28563094-C-T

127881846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28562981-T-C

127882353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28562682-A-G

127882643-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28562411-T-A

http://identifiers.org/hco/6/GRCh38#127882801-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28562247-A-C

127882827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28562221-G-A

http://identifiers.org/hco/6/GRCh38#127882838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28562210-C-A

127884523-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28560879-C-G

127884523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28560879-C-T

127884906-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28560469-G-C

127885252-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28560272-A-T

127885283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28560239-T-C

127885496-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28560042-T-A

127885504-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28560033-T-G

127885580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28559981-A-G

127885674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28559896-T-C

127890781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: -T-C

127892001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28553967-C-T

127892019-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28553949-T-G

127892031-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28553937-T-A

127892031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28553937-T-C

http://identifiers.org/hco/6/GRCh38#127892184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28553818-C-A

127892322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28553667-T-C

127892367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28553583-G-A

127892367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28553583-G-T

127892534-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28553395-G-T

127892741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28553184-G-A

127892868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28552907-T-C

127892932-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28552816-T-G

127892947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28552786-T-C

127892961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28552695-T-C

127893007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28552619-C-T

127893137-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28552392-G-C

127893334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28552191-T-C

127893403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28552135-A-G

127893462-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28552074-T-G

127893511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28552029-T-C

127893576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28551966-G-A

127893576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28551966-G-T

127893651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28551905-T-C

127893713-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28551845-T-A

127894284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28551790-C-T

127894421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28551657-C-T

127894584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28551356-T-C

http://identifiers.org/hco/6/GRCh38#127894696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28551237-C-A

127895381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28550269-G-A

127895398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28550252-A-G

127895400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28550250-T-C

127895458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28550190-G-A

127895585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28550047-G-T

127895915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28549694-A-G

http://identifiers.org/hco/6/GRCh38#127895971-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28549627-A-C

127895973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28549625-T-C

127896029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28549546-C-T

http://identifiers.org/hco/6/GRCh38#127896040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28549535-C-A

127896040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28549535-C-T

127896542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28549070-A-G

127896640-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28548975-T-G

127896809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28548813-A-G

127897230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28548166-C-T

127897258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28548138-A-G

127897302-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28548092-T-A

127897302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28548092-T-C

127897325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28548069-G-T

127897511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28547925-T-C

127898028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28547193-C-T

127898065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28547156-G-A

127900169-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28545523-G-C

127900464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28545258-G-A

http://identifiers.org/hco/6/GRCh38#127900517-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28545163-A-C

127900680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28544982-T-C

127900711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28544940-A-G

127900711-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28544940-A-T

127900807-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28544780-T-A

127900807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28544780-T-C

127900993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 28544592-C-T

127901025-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 28544561-T-G

http://identifiers.org/hco/6/GRCh38#127901053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28544538-C-A

127901071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 28544521-G-A

127901071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 28544521-G-T

127901157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28544353-G-A

127901157-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28544353-G-C

127901157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28544353-G-T

127901217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28544283-T-C

127901414-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28544113-T-A

127902716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28542887-C-T

127903026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28542549-C-T

127903039-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28542535-T-G

127903041-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28542533-A-T

127903151-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28542420-A-T

127903233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28542339-T-C

http://identifiers.org/hco/6/GRCh38#127903398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28542248-C-A

127903398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28542248-C-T

127903495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28542154-A-G

127906449-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28539400-T-A

127906471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28539375-T-C

127906769-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28538723-G-C

127906878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28538608-A-G

127906889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28538593-G-T

http://identifiers.org/hco/6/GRCh38#127907316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28538217-C-A

127907332-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28538201-C-G

127907332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28538201-C-T

127907336-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28538198-G-T

127907526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28538040-G-T

127907559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28538006-A-G

127908590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28536974-C-T

127908628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28536937-A-G

127908795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28536788-T-C

127908856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28536735-A-G

127908856-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28536735-A-T

127908880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28536711-A-G

127908919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28536670-T-C

127908944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28536646-T-C

127909108-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28536489-T-A

127909714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28535978-G-A

127909715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28535977-G-A

127909715-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28535977-G-T

127909751-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28535937-T-A

http://identifiers.org/hco/6/GRCh38#127909755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28535933-C-A

127909755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28535933-C-T

http://identifiers.org/hco/6/GRCh38#127909898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#28535813-C-A

127909898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron_variant, undefined
orthologous variants: 28535813-C-T

127909920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron_variant, undefined
orthologous variants: 28535791-G-T

127909940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron_variant, undefined
orthologous variants: 28535770-T-C

http://identifiers.org/hco/6/GRCh38#127909984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#28535730-C-A

http://identifiers.org/hco/6/GRCh38#127910034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#28535669-C-A

127910301-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28535397-C-G

127910569-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28535147-T-A

127910569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28535147-T-C

127913162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28531825-G-A

127913162-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28531825-G-C

127913162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28531825-G-T

127913384-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28530922-A-T

127913740-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28530592-G-C

127913823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28530517-T-C

127915038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28529663-T-C

http://identifiers.org/hco/6/GRCh38#127915197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28529524-C-A

127915197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28529524-C-T

127915237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28529493-T-C

127916309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28528983-T-C

http://identifiers.org/hco/6/GRCh38#127916429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#28528907-C-A

127916954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28528458-G-A

127917053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28528342-G-A

127917053-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28528342-G-C

127917053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28528342-G-T

127917067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28528328-G-T

127917327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28528107-C-T

127917484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28527987-G-A

127917725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28527756-C-T

127917850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28527645-T-C

127917933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21569
most severe consequence: intron variant
orthologous variants: 28527557-A-G