118994559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron variant
orthologous variants: 54197912-A-G

http://identifiers.org/hco/8/GRCh38#118994597-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54197948-A-C

118994597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron variant
orthologous variants: 54197948-A-G

118994635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron variant
orthologous variants: 54197990-G-A

http://identifiers.org/hco/8/GRCh38#118994747-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54198087-A-C

118994747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron variant
orthologous variants: 54198087-A-G

118994783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron variant
orthologous variants: 54198123-C-T

118994979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron variant
orthologous variants: 54198651-G-A

118995000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron variant
orthologous variants: 54198668-G-T

118995156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron variant
orthologous variants: 54198804-T-C

118995192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron variant
orthologous variants: 54198842-G-A

118995335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron variant
orthologous variants: 54198978-T-C

118995385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron variant
orthologous variants: 54199033-G-A

118995392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron variant
orthologous variants: 54199040-G-A

118995392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron variant
orthologous variants: 54199040-G-T

http://identifiers.org/hco/8/GRCh38#118995431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54199079-C-A

118995540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54199217-G-T

118995604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54199281-T-C

118995610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54199287-T-C

118995710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54199384-T-C

118995768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54199442-G-A

118995853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54199514-C-T

http://identifiers.org/hco/8/GRCh38#118997600-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54209696-A-C

118997627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54209724-C-T

118997641-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54209738-T-G

118997770-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54209856-C-G

118998475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54210618-G-A

118998476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54210619-C-T

118999719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54211552-G-A

http://identifiers.org/hco/8/GRCh38#118999900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54211711-C-A

118999973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54211779-A-G

119001787-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54211929-T-A

http://identifiers.org/hco/8/GRCh38#119001990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54212110-C-A

119002136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54212254-G-T

119002313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54212454-T-C

119002791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54212916-G-A

119002867-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54213353-T-A

119002867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54213353-T-C

http://identifiers.org/hco/8/GRCh38#119002944-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54213430-A-C

119002970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54213459-A-G

http://identifiers.org/hco/8/GRCh38#119003119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54213587-C-A

http://identifiers.org/hco/8/GRCh38#119003129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54213598-C-A

119003129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54213598-C-T

119003298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54213793-A-G

119003459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54213963-C-T

119003597-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54214550-G-C

119003680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54214629-G-A

http://identifiers.org/hco/8/GRCh38#119003738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54214687-C-A

119003762-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54214711-T-A

119003893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54214870-C-T

119004029-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54215057-C-G

119004036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54215064-A-G

119004289-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54215316-C-G

119004453-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54216545-C-G

119004453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54216545-C-T

119004586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54216661-T-C

119004807-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54216882-A-T

119004946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54217010-T-C

119005120-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54217203-T-G

119005542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54217524-G-A

119005651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54217890-G-A

119006369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54222309-T-C

119006474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54222413-G-T

119006559-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54222492-G-C

119006559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54222492-G-T

119006659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54222588-C-T

119006736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54222636-C-T

http://identifiers.org/hco/8/GRCh38#119006737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54222637-C-A

119006932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54222798-A-G

119006966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54222830-G-A

119007042-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54222887-C-G

119007150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54222993-C-T

119007386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54223306-A-G

119007523-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54223457-A-T

119007617-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54223550-T-A

119007618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54223551-T-C

119007953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54223869-A-G

http://identifiers.org/hco/8/GRCh38#119008000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54223905-C-A

119008142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54224008-G-T

119008285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54224165-A-G

119008645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54224514-G-A

119008883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54224721-G-A

119008888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54224726-C-T

119009025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54224869-T-C

119018195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54225406-A-G

119018526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54225734-T-C

119018544-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54225752-C-G

119018580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54225788-G-A

119018665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54225873-T-C

119019109-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54226364-T-G

119019309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54226560-C-T

119019450-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54226700-G-C

119019550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54226781-G-A

119019648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54226876-A-G

http://identifiers.org/hco/8/GRCh38#119019664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54226892-C-A

119020076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54228370-A-G

119020160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54228452-G-A

119020241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54228522-C-T

119020334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54228612-G-A

119020334-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54228612-G-C

119020338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54228616-A-G

119020465-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54228741-T-A

119020482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54228758-A-G

119020546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54228819-C-T

119020557-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54228838-G-C

119020557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54228838-G-T

119020573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54228841-G-A

119020573-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54228841-G-C

119020663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54228931-A-G

119020993-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54229280-T-G

119021010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54229297-T-C

119021015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54229302-G-A

119021035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54229321-A-G

http://identifiers.org/hco/8/GRCh38#119021136-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54229422-C-A

119021326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54229612-G-A

119021411-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54229696-C-G

119021451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54229736-G-A

119021482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54229766-T-C

119021521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54229805-G-A

119021818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54230463-C-T

119021847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54230492-A-G

119021970-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54230620-T-G

http://identifiers.org/hco/8/GRCh38#119022016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54230666-C-A

119022837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54230944-T-C

119022850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54230953-C-T

119022917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54231004-T-C

http://identifiers.org/hco/8/GRCh38#119023059-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54231115-A-C

119023295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54231313-A-G

http://identifiers.org/hco/8/GRCh38#119023335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54231353-C-A

119023355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54231374-T-C

http://identifiers.org/hco/8/GRCh38#119023430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54231455-C-A

119023724-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54231753-T-G

119023851-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54231861-T-A

119023890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54231888-G-T

119024254-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54232192-C-G

119024801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54232641-G-T

119024828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54232642-G-A

http://identifiers.org/hco/8/GRCh38#119024942-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54232717-C-A

119024942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54232717-C-T

http://identifiers.org/hco/8/GRCh38#119024974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54232749-C-A

http://identifiers.org/hco/8/GRCh38#119025352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54233130-C-A

http://identifiers.org/hco/8/GRCh38#119025582-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54233360-A-C

119025582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54233360-A-G

119025707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54233485-G-T

119025722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54233499-C-T

119025869-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54233800-C-G

119025882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54233813-T-C

119025979-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54233925-A-T

119025987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54233933-T-C

119026033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54233973-T-C

119026075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54234015-A-G

119026131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54234067-T-C

119029479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54235577-G-T

119029621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54235721-C-T

119029713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54235809-C-T

119029719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54235815-A-G

119029824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54235918-C-T

119029900-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54235994-T-A

119029900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54235994-T-C

119029998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54236090-T-C

119030007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54236099-G-A

119030051-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54236144-C-G

119034855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54236810-T-C

119034985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54236966-G-A

119034985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54236966-G-T

http://identifiers.org/hco/8/GRCh38#119035393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54237366-C-A

http://identifiers.org/hco/8/GRCh38#119035641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54237606-C-A

119035675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54237640-T-C

119035910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54237869-C-T

119035926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54237885-T-C

119035938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54237897-T-C

119036088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54238049-G-A

119036088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54238049-G-T

http://identifiers.org/hco/8/GRCh38#119036154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54238107-C-A

119036154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54238107-C-T

119036178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54238131-A-G

119036280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54238235-G-A

119036402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54238363-C-T

119038108-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54238535-C-G

119038108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54238535-C-T

119038214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54238660-G-A

http://identifiers.org/hco/8/GRCh38#119038297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54238736-C-A

119038321-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54238760-C-G

119038372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54238813-T-C

119038405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54238842-G-T

119038500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54238938-G-A

119038570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54239012-A-G

119038572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54239014-T-C

119038632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54241751-A-G

119038642-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54241764-T-A

119038674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54241792-T-C

119038753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54241859-C-T

119038800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54241914-G-A

http://identifiers.org/hco/8/GRCh38#119039274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54242412-C-A

119039274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54242412-C-T

119039703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54242845-A-G

119039906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54243086-G-A

119039917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54243131-T-C

119039919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54243133-G-A

119039999-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54243323-T-A

119039999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54243323-T-C

119040089-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54243412-T-G

http://identifiers.org/hco/8/GRCh38#119040704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54244019-C-A

119040704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54244019-C-T

119041050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54244431-G-A

119041058-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54244439-C-G

119041470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54244857-C-T

119041537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54244900-A-G

119041552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54244915-C-T

119041559-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54244922-C-G

119041664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54245025-C-T

119041713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54245103-A-G

119041722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54245112-C-T

119041854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54245238-A-G

119041886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54245269-G-T

119041889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54245272-T-C

119041956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54245346-G-A

119041956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54245346-G-T

119041980-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54245363-G-C

119042314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54245388-G-A

119044274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54248646-T-C

119044445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54248804-G-A

119044445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54248804-G-T

119044517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54248870-T-C

119044558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54248910-T-C

119044976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54249329-A-G

http://identifiers.org/hco/8/GRCh38#119045013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54249344-C-A

119045109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54249444-T-C

119045202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54249541-T-C

119045202-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54249541-T-G

119045410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54249813-C-T

119045483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54249887-G-A

119045513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54249919-G-A

119045516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54249922-T-C

119045796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54250201-T-C

119046145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54250550-G-A

119046216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54250618-C-T

119046388-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54250794-T-G

119046423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54250825-A-G

http://identifiers.org/hco/8/GRCh38#119047905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54251957-C-A

119052188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54254588-A-G

119052431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54254847-A-G

119052664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54255080-C-T

119052720-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54255135-A-T

119052786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54255202-A-G

119052826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54255242-G-A

119052826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54255242-G-T

119052932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54255348-G-T

119052983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54255401-G-A

119052993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54255410-A-G

119053005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54255422-G-A

119053109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54255509-C-T

119053384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54256013-T-C

119053442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54256077-G-A

119053442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54256077-G-T

119053750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54256341-A-G

119053785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54256375-T-C

119054355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54256412-G-A

119054407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54256459-C-T

http://identifiers.org/hco/8/GRCh38#119054601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#54256619-C-A

119054787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54257037-C-T

119055244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54257459-A-G

119055335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54257544-T-C

119055376-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54257585-A-T

119055451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54257658-G-A

119056795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54259634-G-A

119056829-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54259668-G-C

119056838-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54259677-A-T

119056850-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54259689-A-T

119057730-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54260245-A-T

119058194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54260685-G-A

119058383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54260906-C-T

http://identifiers.org/hco/8/GRCh38#119058495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54260999-C-A

119058506-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54261010-A-T

119058690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54261187-A-G

119058727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54261219-T-C

119058759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54261252-G-A

119058872-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54261368-T-G

119058944-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54261440-T-G

119059072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54261553-C-T

119059180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54261721-A-G

http://identifiers.org/hco/8/GRCh38#119059194-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54261736-A-C

http://identifiers.org/hco/8/GRCh38#119059827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54262877-C-A

119059925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54262926-T-C

119059957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54262958-T-C

119059984-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54262985-A-T

119060150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54263151-C-T

119060238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54263228-A-G

119060697-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54263721-C-G

119060723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54263765-G-A

119060758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54263813-C-T

119060776-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54263828-A-T

119061070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54266053-C-T

119061081-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54266064-T-G

119061650-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54266730-C-G

119061868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54266897-A-G

119061933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54266969-A-G

119062189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54267210-A-G

119062205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54267226-G-A

119062366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54267380-C-T

119063104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54268206-G-A

119063376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54268478-G-T

119063727-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54268813-T-A

119063727-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54268813-T-G

http://identifiers.org/hco/8/GRCh38#119063731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54268817-C-A

119064085-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54269149-T-A

119064136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54269203-A-G

119064136-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54269203-A-T

119064370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54271663-A-G

119064692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54271971-T-C

119064699-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54271978-T-G

http://identifiers.org/hco/8/GRCh38#119066090-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54272539-A-C

119066090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54272539-A-G

119066341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54273267-T-C

119066351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54273277-G-A

119066391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54273322-C-T

119066495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54273401-C-T

119066838-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54273727-A-T

119066932-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54273812-A-T

119066973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54273849-G-A

119067016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54273892-G-A

119067156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54274040-T-C

119067244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54274136-G-T

119067247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54274139-A-G

119067360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 54274252-G-A

119067360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 54274252-G-T

119067369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 54274261-A-G

http://identifiers.org/hco/8/GRCh38#119067482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54274369-C-A

119067523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54274409-T-C

119067548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54274434-T-C

119067595-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54274467-T-A

119067595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54274467-T-C

119067612-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54274487-T-A

119067856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54274707-T-C

http://identifiers.org/hco/8/GRCh38#119067878-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54274729-A-C

119067878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54274729-A-G

119067952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54274799-T-C

http://identifiers.org/hco/8/GRCh38#119067995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54274840-C-A

119067995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54274840-C-T

119068055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54274909-T-C

119068135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54275027-C-T

119068361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54275259-G-A

119068361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54275259-G-T

119068984-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54276406-A-T

119068987-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54276409-A-T

119069184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54276597-T-C

119069221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54276623-T-C

119069950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54276928-T-C

119069971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54276950-T-C

119070741-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54277473-A-T

http://identifiers.org/hco/8/GRCh38#119070837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54277525-C-A

119070837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54277525-C-T

119070948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54277637-C-T

119071009-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54277691-G-C

http://identifiers.org/hco/8/GRCh38#119071165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54277838-C-A

119072525-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54278100-A-T

119072529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54278104-C-T

119072644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54278227-C-T

119072796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54278398-T-C

http://identifiers.org/hco/8/GRCh38#119073003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54278602-C-A

119073343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54278897-A-G

119073557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54279005-T-C

119073756-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54279192-T-G

119073957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54279357-T-C

119073982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54279382-G-A

119074264-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54279476-G-C

119074384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54279559-C-T

119074630-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54279765-C-G

119074710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54279844-T-C

119074752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54279886-C-T

119074814-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54279946-G-C

119074852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54279968-G-A

119075059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54280431-G-A

119075097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54280479-C-T

119075142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54280520-C-T

119075407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54280778-A-G

119076632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54281312-C-T

119077082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54281711-A-G

119077143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54281763-G-A

119077168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54281790-G-A

119080188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54287210-C-T

119080255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54287270-C-T

119080311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54287334-G-A

http://identifiers.org/hco/8/GRCh38#119080495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54287496-C-A

119080531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54287532-T-C

119080580-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54287576-A-T

119080586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54287582-A-G

119080586-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54287582-A-T

119080615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54287607-C-T

119081030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54289752-T-C

119081212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54290374-T-C

http://identifiers.org/hco/8/GRCh38#119081471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54290719-C-A

119081471-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54290719-C-G

119081471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54290719-C-T

119081745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54290931-G-A

119081947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54291116-A-G

119081951-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54291120-T-A

119081962-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54291131-G-C

http://identifiers.org/hco/8/GRCh38#119082237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54291433-C-A

119082249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54291442-C-T

119082596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54291788-C-T

119083174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54292310-A-G

119083219-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54292358-G-C

119083358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54292488-C-T

119083509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54292539-G-T

119083510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54292540-A-G

119083543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54292575-A-G

119083548-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54292580-T-A

119083548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54292580-T-C

119084287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54293736-G-A

119084287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54293736-G-T

119084292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54293741-G-A

119084294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54293743-C-T

http://identifiers.org/hco/8/GRCh38#119084472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54293905-C-A

119084764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54294198-T-C

119084978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54294411-C-T

119085240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54294648-G-A

http://identifiers.org/hco/8/GRCh38#119086164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54295135-C-A

119086164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54295135-C-T

119086330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54295322-T-C

119086362-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54295343-C-G

119086468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54295429-C-T

119086969-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54295877-T-A

119086969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54295877-T-C

119087155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54296063-T-C

119087405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54296345-A-G

119087573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54296535-A-G

119087624-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54296575-C-G

119087624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54296575-C-T

119087707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54296661-T-C

119087954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54296933-C-T

http://identifiers.org/hco/8/GRCh38#119087986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54296947-C-A

http://identifiers.org/hco/8/GRCh38#119088020-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54296969-A-C

119088286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54297020-A-G

http://identifiers.org/hco/8/GRCh38#119088403-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54297132-C-A

119088403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54297132-C-T

119088638-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54297175-T-G

http://identifiers.org/hco/8/GRCh38#119088680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54297217-C-A

119088680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54297217-C-T

119088745-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54297282-C-G

119088902-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54297435-T-G

119088937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54297470-A-G

119089121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54297661-T-C

119089276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54297810-T-C

http://identifiers.org/hco/8/GRCh38#119089289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54297825-C-A

119089529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54298264-G-A

http://identifiers.org/hco/8/GRCh38#119089608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54298325-C-A

119089608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54298325-C-T

119089773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54298481-T-C

119089794-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54298538-G-C

119089794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54298538-G-T

119089798-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54298560-T-G

119089807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54298569-T-C

119089807-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54298569-T-G

http://identifiers.org/hco/8/GRCh38#119089814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54298576-C-A

119089814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54298576-C-T

119089818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54298580-G-A

http://identifiers.org/hco/8/GRCh38#119089820-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54298582-C-A

119089820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54298582-C-T

119089828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54298590-T-C

119089849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54298609-T-C

http://identifiers.org/hco/8/GRCh38#119089853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54298613-C-A

119089853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54298613-C-T

http://identifiers.org/hco/8/GRCh38#119089855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54298615-C-A

119089855-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54298615-C-G

http://identifiers.org/hco/8/GRCh38#119089872-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54298632-A-C

http://identifiers.org/hco/8/GRCh38#119089891-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54298651-A-C

119089901-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54298661-T-A

119089901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54298661-T-C

119089958-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54298717-T-A

119089958-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54298717-T-G

119090009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54298760-G-A

119090051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54298818-C-T

119090071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54298855-A-G

119090129-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54298986-T-A

119090183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54299114-G-A

119090325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54299251-T-C

119090524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54299440-T-C

http://identifiers.org/hco/8/GRCh38#119090865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54300221-C-A

http://identifiers.org/hco/8/GRCh38#119090866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54300222-C-A

119090866-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54300222-C-G

119090889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54300245-A-G

http://identifiers.org/hco/8/GRCh38#119091054-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54302460-A-C

119091054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54302460-A-G

119091078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54302484-A-G

http://identifiers.org/hco/8/GRCh38#119091114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54302521-C-A

119091114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54302521-C-T

http://identifiers.org/hco/8/GRCh38#119091124-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54302531-A-C

119091131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54302537-A-G

http://identifiers.org/hco/8/GRCh38#119091232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54302638-C-A

119091232-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54302638-C-G

119091232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54302638-C-T

119091867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54302893-A-G

119091927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54302969-T-C

119092048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54303065-G-T

119092054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54303071-A-G

119092498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54303190-C-T

119092952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54303386-G-T

119093068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54303508-G-A

119093075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54303515-C-T

119093202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54303646-A-G

119093241-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54303684-T-G

http://identifiers.org/hco/8/GRCh38#119093242-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54303685-A-C

119093293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54303735-C-T

119093316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54303758-G-T

119093354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54303795-G-A

119093354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54303795-G-T

119093453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54303845-G-A

119093505-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54303895-T-A

119093508-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54303898-T-A

119093631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54304035-A-G

119093678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54304080-T-C

119093750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54304122-A-G

119093994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54304319-T-C

119094004-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54304329-T-G

119094153-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54304449-T-A

119094189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54304485-G-A

119094282-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54304578-T-A

119094587-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54304844-G-C

119094617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54304874-G-A

119094628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54304891-G-A

119094641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54304904-G-A

119094694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54304955-T-C

119094825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54305082-A-G

119094936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54305190-G-A

119094965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54305219-A-G

http://identifiers.org/hco/8/GRCh38#119095000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54305254-C-A

119095106-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54305361-G-C

119098251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54306234-G-A

119098251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54306234-G-T

119098331-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54306315-T-A

119098377-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54306357-A-T

119098400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54306383-T-C

119098714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54314176-A-G

119099146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54314603-T-C

119099190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54314648-A-G

119099208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54314666-C-T

119099313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54314770-C-T

119099506-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54314926-A-T

http://identifiers.org/hco/8/GRCh38#119099515-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54314935-A-C

119099515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54314935-A-G

119099538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54314948-G-T

119099759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54315140-C-T

119099810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54315191-C-T

119099919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54318050-T-C

119099941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54318072-T-C

119099950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54318080-G-A

119100070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54318199-T-C

119100218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54318786-G-T

119100482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54319027-T-C

119100718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54319249-C-T

119100843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54319363-C-T

119100874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54319395-C-T

http://identifiers.org/hco/8/GRCh38#119101037-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54319554-A-C

119101057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54319574-G-A

119101437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54319904-C-T

119101459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54319928-A-G

119101664-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54320135-A-T

http://identifiers.org/hco/8/GRCh38#119101722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54320193-C-A

119101722-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54320193-C-G

http://identifiers.org/hco/8/GRCh38#119101943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54320435-C-A

119101943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54320435-C-T

119101952-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54320444-G-C

119102023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54320509-C-T

119102290-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54320695-T-A

119102290-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54320695-T-G

http://identifiers.org/hco/8/GRCh38#119102316-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54320721-A-C

119102316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54320721-A-G

119102316-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54320721-A-T

http://identifiers.org/hco/8/GRCh38#119102454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54320858-C-A

119102454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54320858-C-T

http://identifiers.org/hco/8/GRCh38#119102520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54320949-C-A

119102533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54320961-G-T

http://identifiers.org/hco/8/GRCh38#119102559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54320987-C-A

119102568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54320996-G-A

119102568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54320996-G-T

119102585-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54321013-T-G

119102680-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54321109-G-C

119102680-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54321109-G-T

http://identifiers.org/hco/8/GRCh38#119102708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54321136-C-A

119102708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54321136-C-T

119102735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54321153-G-A

119102735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54321153-G-T

119102804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54321217-A-G

119102808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54321221-T-C

http://identifiers.org/hco/8/GRCh38#119102820-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54321233-A-C

119102820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54321233-A-G

119102820-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54321233-A-T

119102936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54321335-T-C

119102965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54321365-C-T

119103237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54321637-T-C

119103304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54321703-T-C

119103505-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54321899-T-A

119103567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54321951-A-G

http://identifiers.org/hco/8/GRCh38#119103593-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54322924-C-A

119103594-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54322925-A-T

http://identifiers.org/hco/8/GRCh38#119103770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54323093-C-A

http://identifiers.org/hco/8/GRCh38#119103803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54323128-C-A

119103803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 54323128-C-T

119103834-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 54323159-T-G

119103873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: synonymous variant
orthologous variants: 54323198-A-G

119103873-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: synonymous variant
orthologous variants: 54323198-A-T

http://identifiers.org/hco/8/GRCh38#119103901-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54323226-C-A

119103901-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron variant
orthologous variants: 54323226-C-G

119103901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron variant
orthologous variants: 54323226-C-T

119103920-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron variant
orthologous variants: 54323250-T-A

119103920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron variant
orthologous variants: 54323250-T-C

119103991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron variant
orthologous variants: 54323312-A-G

119104265-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron variant
orthologous variants: 54323988-C-G

119104517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron variant
orthologous variants: 54324217-C-T

119104608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron variant
orthologous variants: 54324298-T-C

119104649-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron variant
orthologous variants: 54324339-A-T

119104714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron variant
orthologous variants: 54324404-T-C

119104790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron variant
orthologous variants: 54324485-G-T

119104909-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron variant
orthologous variants: 54324817-A-T

119104967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron variant
orthologous variants: 54324856-G-A

119105445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron variant
orthologous variants: 54325299-G-A

119105779-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron variant
orthologous variants: 54325593-C-G

119105779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: intron variant
orthologous variants: 54325593-C-T

119105966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: synonymous variant
orthologous variants: 54325780-C-T

119106067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: missense variant
orthologous variants: 54325881-G-A

119106086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: synonymous variant
orthologous variants: 54325900-T-C

119106107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: synonymous variant
orthologous variants: 54325921-G-A

http://identifiers.org/hco/8/GRCh38#119106358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54326146-C-A

119106374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: 3 prime UTR variant
orthologous variants: 54326162-G-T

119106909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: 3 prime UTR variant
orthologous variants: 54326202-C-T

119107025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: 3 prime UTR variant
orthologous variants: 54326318-C-T

http://identifiers.org/hco/8/GRCh38#119107056-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54326346-A-C

http://identifiers.org/hco/8/GRCh38#119107129-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54326415-A-C

119107144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: 3 prime UTR variant
orthologous variants: 54326430-A-G

119107192-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: 3 prime UTR variant
orthologous variants: 54326487-T-G

119107228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: 3 prime UTR variant
orthologous variants: 54326523-C-T

119107280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: 3 prime UTR variant
orthologous variants: 54326564-C-T

119107428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: 3 prime UTR variant
orthologous variants: 54326712-C-T

119107503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: 3 prime UTR variant
orthologous variants: 54326787-C-T

119107523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: 3 prime UTR variant
orthologous variants: 54326807-G-A

119107939-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: 3 prime UTR variant
orthologous variants: 54327168-G-C

119108064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: 3 prime UTR variant
orthologous variants: 54327289-A-G

119108134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2220
most severe consequence: 3 prime UTR variant
orthologous variants: 54327368-T-C