http://identifiers.org/hco/8/GRCh38#29673967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#34992801-C-A

29673971-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: non coding transcript exon variant
orthologous variants: 34992797-T-A

29674113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: non coding transcript exon variant
orthologous variants: 34992650-G-A

29674113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: non coding transcript exon variant
orthologous variants: 34992650-G-T

29674201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: non coding transcript exon variant
orthologous variants: 34992564-A-G

29674260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: non coding transcript exon variant
orthologous variants: 34992505-G-A

29674260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: non coding transcript exon variant
orthologous variants: 34992505-G-T

http://identifiers.org/hco/8/GRCh38#29674343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#34992423-C-A

29674343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: non coding transcript exon variant
orthologous variants: 34992423-C-T

29674578-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34992189-G-C

29675417-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34991540-G-C

29675584-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34991382-C-G

29675584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34991382-C-T

29675750-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34991215-G-C

http://identifiers.org/hco/8/GRCh38#29675922-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#34991074-A-C

29675922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34991074-A-G

29675922-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34991074-A-T

29677249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34990665-T-C

29677998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: non coding transcript exon variant
orthologous variants: 34989648-T-C

29677998-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: non coding transcript exon variant
orthologous variants: 34989648-T-G

29678036-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34989613-A-T

29678119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34989529-G-T

29678136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34989512-T-C

29683282-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34988148-C-G

29683294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34988139-A-G

http://identifiers.org/hco/8/GRCh38#29683639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#34987834-C-A

29683699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34987774-G-A

29683815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34987655-A-G

29684087-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34987088-A-T

29684262-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34986662-G-C

29684291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34986634-T-C

29684341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34986584-C-T

29684464-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34986464-A-T

29684493-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34986421-T-A

29684528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34986371-T-C

29684653-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34986262-T-G

29684692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34986222-C-T

29684776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34986146-T-C

29684801-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34986121-T-G

29687174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34985972-T-C

http://identifiers.org/hco/8/GRCh38#29687191-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#34985946-A-C

29687191-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34985946-A-T

http://identifiers.org/hco/8/GRCh38#29687209-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#34985928-A-C

29687209-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34985928-A-T

http://identifiers.org/hco/8/GRCh38#29687314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#34985820-C-A

29688516-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34984324-C-G

http://identifiers.org/hco/8/GRCh38#29693752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#34969609-C-A

29693752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34969609-C-T

29693936-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34969714-A-T

29693938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34969716-G-T

29694275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34970041-A-G

29694389-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34970161-A-T

29694405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34970177-G-T

29695033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34972773-T-C

29695227-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34972926-C-G

http://identifiers.org/hco/8/GRCh38#29695314-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#34972994-A-C

29695340-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34973019-C-G

29695373-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34973048-G-C

29695410-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34973079-C-G

29696212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34973807-C-T

29696515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34974151-A-G

29697266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34976203-G-A

29697266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34976203-G-T

29697556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34976408-G-T

29698488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34976722-C-T

29698494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34976729-G-T

29698768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34976978-T-C

http://identifiers.org/hco/8/GRCh38#29699297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#34977472-C-A

http://identifiers.org/hco/8/GRCh38#29699401-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#34977567-A-C

29699518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34977679-A-G

29699524-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34977685-A-T

29699540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34977701-A-G

29699560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34977717-A-G

29699952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34977836-T-C

http://identifiers.org/hco/8/GRCh38#29699954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#34977838-C-A

29700504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34978363-C-T

29700665-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34978516-T-A

29700701-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34978551-T-A

29710352-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34965725-T-A

29710425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34965646-G-T

29710472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34965600-C-T

29710505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34965577-A-G

29710574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34965512-T-C

29710634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34965444-G-A

29712506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34962994-T-C

29712551-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34962945-G-C

29712606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34962900-T-C

29713492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34962030-G-A

http://identifiers.org/hco/8/GRCh38#29717429-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#34957099-A-C

29717429-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34957099-A-T

29717568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34956762-T-C

29717714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34956620-G-A

29717714-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34956620-G-C

29717722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34956611-T-C

29717781-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34956546-T-A

http://identifiers.org/hco/8/GRCh38#29717900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#34956433-C-A

29717900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34956433-C-T

29718079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34956274-G-A

29718355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34956049-A-G

29718369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34956035-G-A

29718398-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34956005-T-G

29720994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34954486-G-A

29721220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34954240-A-G

29721229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34954234-G-A

29721229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34954234-G-T

http://identifiers.org/hco/8/GRCh38#29721305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#34954161-C-A

http://identifiers.org/hco/8/GRCh38#29721408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#34954059-C-A

29721456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34954034-G-A

29721456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34954034-G-T

29721497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34953993-G-T

http://identifiers.org/hco/8/GRCh38#29721502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#34953988-C-A

29721502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34953988-C-T

http://identifiers.org/hco/8/GRCh38#29721593-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#34953930-C-A

29721593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34953930-C-T

29721631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34953890-A-G

29721660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34953865-G-T

29721848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34953671-G-A

29721878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34953639-T-C

29721931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34953589-G-A

29721931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34953589-G-T

http://identifiers.org/hco/8/GRCh38#29721932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#34953588-C-A

29721979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34953542-C-T

29721984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34953537-T-C

http://identifiers.org/hco/8/GRCh38#29722029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#34953493-C-A

29722083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34953455-G-T

http://identifiers.org/hco/8/GRCh38#29722084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#34953454-C-A

29722084-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34953454-C-G

http://identifiers.org/hco/8/GRCh38#29722092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#34953446-C-A

29722092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34953446-C-T

29722179-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34953354-A-T

http://identifiers.org/hco/8/GRCh38#29722432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#34953087-C-A

29722676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34952705-C-T

http://identifiers.org/hco/8/GRCh38#29723040-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#34952433-A-C

29723076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34952392-T-C

29723076-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34952392-T-G

http://identifiers.org/hco/8/GRCh38#29723116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#34952352-C-A

29723159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34952307-T-C

29723221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34952239-C-T

29726654-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34950908-T-A

29726786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34950777-G-A

29727174-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34950440-T-A

29727233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34950381-G-A

29727237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34950377-T-C

29727262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34950367-C-T

29727659-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34948716-G-C

29727673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34948702-C-T

http://identifiers.org/hco/8/GRCh38#29727719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#34948665-C-A

29727835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34948310-C-T

29727960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34948186-G-T

http://identifiers.org/hco/8/GRCh38#29728087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#34948076-C-A

http://identifiers.org/hco/8/GRCh38#29728102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#34948061-C-A

29728282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34947878-G-A

29728464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34947705-T-C

http://identifiers.org/hco/8/GRCh38#29728637-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#34947619-A-C

29728650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34947604-A-G

29728707-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34947556-G-C

29730048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34946694-A-G

29730204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34946188-G-T

29730370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34946014-G-T

http://identifiers.org/hco/8/GRCh38#29730416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#34945970-C-A

29730459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34945932-G-A

29730582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34945856-C-T

29730633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34945803-G-T

29730965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34945600-A-G

29730992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34945573-G-T

http://identifiers.org/hco/8/GRCh38#29731000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#34945565-C-A

29731068-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34945504-G-C

29731084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34945490-G-A

29731099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34945475-A-G

29731182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34945382-A-G

http://identifiers.org/hco/8/GRCh38#29732180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#34944656-C-A

29732180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34944656-C-T

29732187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34944649-A-G

29732502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34944379-T-C

29732502-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34944379-T-G

http://identifiers.org/hco/8/GRCh38#29732557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#34944329-C-A

29732588-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34944293-C-G

29732609-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34944272-T-A

http://identifiers.org/hco/8/GRCh38#29732878-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#34944056-A-C

29732878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34944056-A-G

http://identifiers.org/hco/8/GRCh38#29732951-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#34943985-A-C

29733024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34943918-C-T

29734075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34943153-C-T

29734092-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34943116-T-A

29734093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34943115-G-A

29734261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34942938-C-T

29734373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34942832-C-T

29734470-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34942761-C-G

29734690-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34942633-T-A

29734690-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34942633-T-G

29735034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34942092-C-T

http://identifiers.org/hco/8/GRCh38#29735040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#34942086-C-A

29735040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34942086-C-T

29735043-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34942083-T-G

29735054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34942072-G-A

http://identifiers.org/hco/8/GRCh38#29735107-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#34942020-A-C

29735231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34941879-A-G

29735245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34941866-C-T

29735276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34941838-A-G

29735311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34941804-T-C

29735340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34941787-A-G

29735624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34941602-T-C

29735751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34941578-G-A

29735906-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34941496-T-A

29735910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34941492-A-G

29735927-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34941471-G-C

29735927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34941471-G-T

29735979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34941419-T-C

29736141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34941272-T-C

29736357-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34941112-G-T

29736379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34941091-T-C

http://identifiers.org/hco/8/GRCh38#29736718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#34941070-C-A

29736919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34940871-A-G

29737069-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34940694-G-C

29737069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34940694-G-T

29737192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34940558-T-C

29737309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34940438-G-A

29737329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34940404-G-A

29737578-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34940197-C-G

29737618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34940147-G-A

29737908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34939822-G-A

29738008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34939721-G-T

http://identifiers.org/hco/8/GRCh38#29738096-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#34939633-A-C

29738135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34939598-C-T

http://identifiers.org/hco/8/GRCh38#29738195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#34939542-C-A

29739654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34937958-G-T

29739679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34937939-G-A

29739934-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34937709-C-G

29740067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34937387-T-C

29740490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34936995-G-A

29740763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34936743-T-C

29741092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34936440-C-T

29741472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34936080-T-C

29741522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34936032-C-T

29741671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34935916-T-C

29742191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34935724-G-T

http://identifiers.org/hco/8/GRCh38#29742288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#34935640-C-A

29742288-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34935640-C-G

29742539-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34934390-C-G

29743787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34930276-C-T

29743890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34930172-G-T

http://identifiers.org/hco/8/GRCh38#29744300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#34929751-C-A

29744514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34929542-G-A

29744614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34929444-G-A

29744614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34929444-G-T

29744740-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34929330-T-A

29744799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34929271-T-C

29744865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34929172-A-G

29745271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34927969-A-G

29746020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34927300-C-T

29746909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34926558-A-G

29747027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34926456-G-A

29747062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34926421-T-C

29747120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34926365-G-T

29747161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34926320-G-A

29747193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34926288-A-G