http://identifiers.org/hco/5/GRCh38#179111126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50698126-C-A

179111126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: 50698126-C-T

179111138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: 50698114-T-C

179111141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: 50698111-G-A

179111141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: 50698111-G-T

http://identifiers.org/hco/5/GRCh38#179111183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50698086-C-A

179111269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: 50698001-T-C

179111273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: 50697997-G-T

http://identifiers.org/hco/5/GRCh38#179111308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50697943-C-A

179111308-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: 50697943-C-G

179111308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: 50697943-C-T

179111320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: 50697898-G-A

179111320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: 50697898-G-T

179111362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: 50697860-G-A

179111362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: 50697860-G-T

179111377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: 50697847-G-A

179111457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: 50697767-T-C

179111470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: 50697753-C-T

http://identifiers.org/hco/5/GRCh38#179111483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50697738-C-A

179111500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: 50697721-A-G

179111639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: 50697655-G-A

179111702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: 50697592-T-C

179111822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: 50697474-T-C

179111856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: 50697438-G-T

179111921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: 50697391-G-T

179111925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: 50697387-G-T

179111966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: 50697349-G-T

179111971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: 50697344-G-A

179111971-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: 50697344-G-C

http://identifiers.org/hco/5/GRCh38#179111998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50697317-C-A

179111998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: 50697317-C-T

http://identifiers.org/hco/5/GRCh38#179112009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50697304-C-A

179112009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: 50697304-C-T

http://identifiers.org/hco/5/GRCh38#179112015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50697298-C-A

179112015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: 50697298-C-T

179112065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: 50697259-A-G

179112165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: 50697128-G-A

179112216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: 50697064-G-A

179112216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: 50697064-G-T

179112340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: 50696955-T-C

179112366-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: 50696929-T-A

179112366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: 50696929-T-C

http://identifiers.org/hco/5/GRCh38#179112423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50696881-C-A

179112477-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: 50696353-C-G

http://identifiers.org/hco/5/GRCh38#179112655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50696187-C-A

179112766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: 50696069-G-A

179112766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: 50696069-G-T

http://identifiers.org/hco/5/GRCh38#179112890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50695968-C-A

179112890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: 50695968-C-T

179112891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: 50695967-A-G

179112891-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: 50695967-A-T

179112945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: 50695919-T-C

179112949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: 50695915-C-T

179112955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: 50695909-T-C

179113013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: 50695846-G-A

179113013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: 50695846-G-T

http://identifiers.org/hco/5/GRCh38#179113017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50695842-C-A

179113025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: 50695834-A-G

http://identifiers.org/hco/5/GRCh38#179113049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50695812-C-A

179113049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: 50695812-C-T

http://identifiers.org/hco/5/GRCh38#179113079-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50695774-A-C

179113079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: 50695774-A-G

179113080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: 50695773-G-A

http://identifiers.org/hco/5/GRCh38#179113082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50695771-C-A

179113082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: 50695771-C-T

179113097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: 50695756-T-C

179113173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: 50695675-A-G

http://identifiers.org/hco/5/GRCh38#179113194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50695654-C-A

179113217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: 50695634-A-G

http://identifiers.org/hco/5/GRCh38#179113220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50695631-C-A

179113220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: 50695631-C-T

179113261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: 50695605-A-G

http://identifiers.org/hco/5/GRCh38#179113317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50695547-C-A

179113317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: 50695547-C-T

179113530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: 50695337-A-G

http://identifiers.org/hco/5/GRCh38#179113625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50695241-C-A

179113625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: 50695241-C-T

179113633-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: 50695233-T-A

179113633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: 50695233-T-C

179113716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3 prime UTR variant
orthologous variants: 50695012-T-C

179113904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: missense variant
orthologous variants: 50694817-T-C

179113970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: missense variant
orthologous variants: 50694751-T-C

179113970-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: missense variant
orthologous variants: 50694751-T-G

179113977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: missense variant
orthologous variants: 50694744-G-A

179114119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 50694602-T-C

179114171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 50694550-C-T

179114174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 50694547-G-A

179114174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 50694547-G-T

179114216-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 50694502-T-G

179114255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 50694463-G-A

179114267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 50694451-T-C

179114645-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50694097-G-C

http://identifiers.org/hco/5/GRCh38#179114654-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50694088-A-C

179114948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50693844-A-G

179114986-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50693807-C-G

179115228-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50693589-A-T

http://identifiers.org/hco/5/GRCh38#179115308-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50693517-A-C

179115314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50693508-C-T

179115401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50693424-A-G

179116482-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50693367-G-C

179116482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50693367-G-T

179116602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50693236-G-A

179116610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50693228-G-A

179116690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50693150-G-A

179116799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50693053-C-T

179116800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50693052-G-A

179116865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50692984-A-G

179117187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50692696-A-G

179117222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50692662-T-C

179117222-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50692662-T-G

http://identifiers.org/hco/5/GRCh38#179117252-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50692635-A-C

179117252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50692635-A-G

179117287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50692602-C-T

179117852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50692020-G-A

179117943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50691930-T-C

179117964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50691909-G-A

179118154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50691723-G-A

179118193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50691692-T-C

http://identifiers.org/hco/5/GRCh38#179118675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50690478-C-A

179118685-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50690468-G-C

http://identifiers.org/hco/5/GRCh38#179118732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50690434-C-A

179119066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50690185-G-A

179119070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50690181-C-T

179119317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50689961-G-A

179119317-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50689961-G-C

179119317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50689961-G-T

179119500-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50689816-G-C

179119583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50689733-T-C

179119848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50689479-C-T

179119864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50689466-G-T

179119985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50689366-G-A

179119985-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50689366-G-C

179120085-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50689263-G-C

179120085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50689263-G-T

179120205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50689135-G-T

179120206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50689134-T-C

http://identifiers.org/hco/5/GRCh38#179120317-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50688994-A-C

179120431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50688864-G-A

179120431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50688864-G-T

http://identifiers.org/hco/5/GRCh38#179120521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50688771-C-A

179120521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50688771-C-T

179121053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50688168-G-T

http://identifiers.org/hco/5/GRCh38#179121150-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50688046-A-C

179121150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50688046-A-G

179121150-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50688046-A-T

179121216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50687969-G-A

http://identifiers.org/hco/5/GRCh38#179121342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50687819-C-A

179121342-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50687819-C-G

179121396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50687663-T-C

http://identifiers.org/hco/5/GRCh38#179121461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50687594-C-A

http://identifiers.org/hco/5/GRCh38#179121606-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50687408-A-C

179121606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 50687408-A-G

179121606-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 50687408-A-T

http://identifiers.org/hco/5/GRCh38#179121786-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50687224-A-C

179121786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50687224-A-G

179121809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50687118-G-T

179121832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50687090-G-A

179121832-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50687090-G-C

179121832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50687090-G-T

179121899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50687041-A-G

http://identifiers.org/hco/5/GRCh38#179121954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50686997-C-A

179121954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50686997-C-T

179122113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50686858-G-A

179122113-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50686858-G-C

http://identifiers.org/hco/5/GRCh38#179122202-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50686776-A-C

179122220-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50686758-G-C

179122253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50686725-G-A

179122253-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50686725-G-C

179122294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50686687-C-T

179122419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50686539-T-C

179122438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50686520-G-A

179122448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50686464-C-T

179122455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50686457-C-T

179122535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50686379-G-A

179122535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50686379-G-T

http://identifiers.org/hco/5/GRCh38#179122543-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50686371-A-C

179122543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50686371-A-G

179122557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50686357-G-T

http://identifiers.org/hco/5/GRCh38#179122559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50686355-C-A

179122559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50686355-C-T

179122569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50686345-T-C

179122605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50686309-G-A

179122605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50686309-G-T

179122673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 50686243-G-A

179122673-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 50686243-G-C

179122673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 50686243-G-T

179122679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 50686237-T-C

http://identifiers.org/hco/5/GRCh38#179122692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/11/GRCm39#50686224-C-A

179122748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 50686168-G-A

179122748-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 50686168-G-C

http://identifiers.org/hco/5/GRCh38#179122847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50686084-C-A

179122847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50686084-C-T

179122849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50686082-G-T

179123135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50684329-A-G

179123354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50684098-A-G

179124652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50683775-G-A

179124728-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50683713-G-C

179124728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50683713-G-T

179124827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 50683614-T-C

179125187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 50683464-G-T

179125200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50683451-C-T

http://identifiers.org/hco/5/GRCh38#179125259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50683425-C-A

179125264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50683420-G-A

179125264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50683420-G-T

179125288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50683396-G-T

http://identifiers.org/hco/5/GRCh38#179125294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50683388-C-A

179125294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50683388-C-T

http://identifiers.org/hco/5/GRCh38#179125298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50683386-C-A

179125298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50683386-C-T

179125423-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50683279-C-G

179125487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50683223-C-T

179125530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50683181-G-A

179125604-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50683116-T-G

179125705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50683023-A-G

http://identifiers.org/hco/5/GRCh38#179125752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50682988-C-A

179125752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50682988-C-T

179125849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50682899-G-A

179125849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50682899-G-T

http://identifiers.org/hco/5/GRCh38#179125861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50682887-C-A

179125861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50682887-C-T

http://identifiers.org/hco/5/GRCh38#179125862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50682886-C-A

179125862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50682886-C-T

179125864-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50682884-T-A

179125864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50682884-T-C

179125864-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50682884-T-G

http://identifiers.org/hco/5/GRCh38#179125908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50682846-C-A

179125908-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50682846-C-G

179125908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50682846-C-T

http://identifiers.org/hco/5/GRCh38#179125912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50682842-C-A

179125912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50682842-C-T

http://identifiers.org/hco/5/GRCh38#179125913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50682841-C-A

179125938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50682828-G-A

179125939-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50682827-A-T

http://identifiers.org/hco/5/GRCh38#179125968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50682801-C-A

179125968-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50682801-C-G

179125968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50682801-C-T

179125973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50682796-G-A

179125973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50682796-G-T

179126027-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 50682731-C-G

179126027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 50682731-C-T

179126030-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 50682728-T-A

http://identifiers.org/hco/5/GRCh38#179126201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50682559-C-A

179126201-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50682559-C-G

179126201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50682559-C-T

179126209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50682549-G-A

179126209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50682549-G-T

179126224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50682534-T-C

179127689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50680014-C-T

179127716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50679987-G-A

179127861-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50679840-T-A

179127861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50679840-T-C

179127880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50679807-G-T

http://identifiers.org/hco/5/GRCh38#179127881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50679806-C-A

179127881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50679806-C-T

http://identifiers.org/hco/5/GRCh38#179127888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50679799-C-A

179127897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50679735-C-T

179128018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 50679580-G-A

179128018-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 50679580-G-C

http://identifiers.org/hco/5/GRCh38#179128191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50679403-C-A

179128209-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50679385-G-C

179129429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50678667-A-G

179129458-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50678645-G-C

179129784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50678337-G-T

179129825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50678307-G-A

179129825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50678307-G-T

http://identifiers.org/hco/5/GRCh38#179129836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50678296-C-A

179129836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50678296-C-T

http://identifiers.org/hco/5/GRCh38#179129841-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50678291-A-C

179129848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50678283-G-T

http://identifiers.org/hco/5/GRCh38#179129874-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50678255-A-C

179129874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50678255-A-G

http://identifiers.org/hco/5/GRCh38#179129881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50678243-C-A

179129881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50678243-C-T

179129902-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50678222-T-G

179129910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50678214-G-A

179129910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50678214-G-T

http://identifiers.org/hco/5/GRCh38#179130102-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50678010-A-C

179132098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50677614-G-T

179132104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50677606-G-A

179132104-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50677606-G-C

179132104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50677606-G-T

179132105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50677605-G-A

179132105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50677605-G-T

http://identifiers.org/hco/5/GRCh38#179132106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50677604-C-A

179132106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50677604-C-T

http://identifiers.org/hco/5/GRCh38#179132143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50677550-C-A

179132169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50677531-C-T

179132221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50677500-G-A

179132345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50677381-A-G

http://identifiers.org/hco/5/GRCh38#179132401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50677328-C-A

179132401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50677328-C-T

http://identifiers.org/hco/5/GRCh38#179132657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50676600-C-A

179132664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50676593-C-T

179132715-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50676552-G-T

179132721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50676547-G-A

179132721-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50676547-G-C

179132725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50676543-G-A

http://identifiers.org/hco/5/GRCh38#179132763-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50676507-A-C

179132785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 50676488-T-C

179132866-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 50676407-T-G

179132904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 50676369-T-C

http://identifiers.org/hco/5/GRCh38#179132924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50676347-C-A

179132924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50676347-C-T

179136073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50675397-G-A

179136073-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50675397-G-C

179136149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50675339-C-T

http://identifiers.org/hco/5/GRCh38#179136150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50675338-C-A

179136175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50675295-G-A

179136175-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50675295-G-C

179136183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50675287-T-C

179136188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50675282-G-A

179137480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50672986-C-T

http://identifiers.org/hco/5/GRCh38#179137528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50672940-C-A

179137528-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50672940-C-G

179137580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50672900-C-T

179137641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50672838-T-C

179137656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50672823-G-T

http://identifiers.org/hco/5/GRCh38#179137722-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50672746-A-C

179137722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50672746-A-G

179137722-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50672746-A-T

http://identifiers.org/hco/5/GRCh38#179137774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50672700-C-A

179137774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 50672700-C-T

179138021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50672462-T-C

179138053-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50672431-G-C

http://identifiers.org/hco/5/GRCh38#179138079-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50672405-C-A

179138079-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50672405-C-G

179138130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50672368-C-T

179138179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50672315-C-T

179138191-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50672303-G-C

179138363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50671806-G-A

179138501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50671666-G-A

http://identifiers.org/hco/5/GRCh38#179138707-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50671455-A-C

179138739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50671427-G-A

179138884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50671270-C-T

179138894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50671260-G-A

http://identifiers.org/hco/5/GRCh38#179139016-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50671167-A-C

179139016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50671167-A-G

179139084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50671095-G-T

http://identifiers.org/hco/5/GRCh38#179139772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50670710-C-A

179139772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50670710-C-T

http://identifiers.org/hco/5/GRCh38#179139797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50670697-C-A

179139797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50670697-C-T

179139910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 50670643-G-A

179148861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50669170-G-A

179148947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50669094-G-A

179148947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50669094-G-T

179149075-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50668985-A-T

179149173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50668897-T-C

179149255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50668838-C-T

179151639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50668658-G-A

179151717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50668613-C-T

179151917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50668382-A-G

179152005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50668193-G-A

179152005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50668193-G-T

179152034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50668164-C-T

179152041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50668157-G-A

179152041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50668157-G-T

179152052-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50668141-C-G

179152052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50668141-C-T

179152062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50668125-G-T

179152065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50668122-T-C

179152082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50668105-G-T

179152129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50668082-G-A

179152149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 50668062-G-A

179152294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50667909-C-T

179152310-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50667892-G-T

179152383-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50667834-T-A

179152415-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50667791-C-G

179152451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50667755-G-A

179153460-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50667614-G-C

179153460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50667614-G-T

http://identifiers.org/hco/5/GRCh38#179153528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50667542-C-A

179153528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 50667542-C-T

179153576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 50667494-G-A

179153576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 50667494-G-T

179153612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 50667458-C-T

179153728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50667362-T-C

179153963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50667172-G-A

179153963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50667172-G-T

179153976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50667154-G-A

179153976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50667154-G-T

http://identifiers.org/hco/5/GRCh38#179153985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50667145-C-A

179153985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50667145-C-T

http://identifiers.org/hco/5/GRCh38#179153993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50667137-C-A

179153993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50667137-C-T

http://identifiers.org/hco/5/GRCh38#179154031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50667106-C-A

179154031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50667106-C-T

179154055-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 50667081-T-A

179154055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 50667081-T-C

http://identifiers.org/hco/5/GRCh38#179154160-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50666976-C-A

179154160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 50666976-C-T

179154210-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50666923-G-C

179154210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50666923-G-T

http://identifiers.org/hco/5/GRCh38#179154211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50666922-C-A

179154211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50666922-C-T

179154240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50666895-G-A

179154240-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50666895-G-T

179154268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50666868-A-G

179154273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50666863-G-A

http://identifiers.org/hco/5/GRCh38#179154308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50666815-C-A

179154308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50666815-C-T

179154349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50666764-A-G

179154366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50666729-C-T

179154388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50666707-G-A

179154528-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50666495-C-G

179154677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50666362-G-A

179154678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50666361-G-A

179154678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50666361-G-T

179154703-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50666345-T-A

179154710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50666338-G-A

179154710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50666338-G-T

http://identifiers.org/hco/5/GRCh38#179154738-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50666312-A-C

179154738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50666312-A-G

179154771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50666295-T-C

179154791-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50666275-C-G

179154791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50666275-C-T

http://identifiers.org/hco/5/GRCh38#179154793-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50666273-A-C

179154953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50666108-C-T

http://identifiers.org/hco/5/GRCh38#179155047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50666049-C-A

179155053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50666044-G-A

179155053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50666044-G-T

179155059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50666038-G-A

179155064-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50666033-G-C

179155064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50666033-G-T

179155125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50666000-C-T

179155162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50665964-C-T

http://identifiers.org/hco/5/GRCh38#179155242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50665883-C-A

179155260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50665871-C-T

http://identifiers.org/hco/5/GRCh38#179158656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50664250-C-A

179158656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50664250-C-T

179158939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50663972-G-A

179158939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50663972-G-T

179158983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50663928-T-C

179158993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50663918-G-T

179158995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50663916-T-C

http://identifiers.org/hco/5/GRCh38#179159031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50663876-C-A

179159031-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50663876-C-G

179159031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50663876-C-T

http://identifiers.org/hco/5/GRCh38#179159040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50663867-C-A

http://identifiers.org/hco/5/GRCh38#179159054-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50663853-A-C

179159054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50663853-A-G

179162985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50663382-G-A

179162986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50663381-G-A

179162987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50663380-G-A

179163070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50663299-C-T

179163096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50663290-G-A

179163555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50662882-T-C

http://identifiers.org/hco/5/GRCh38#179164037-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50662363-A-C

179164458-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50661681-G-C

179167307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50660470-G-A

179167316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50660459-C-T

179167381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50660386-A-G

179167545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50660231-G-A

179167591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50660194-C-T

http://identifiers.org/hco/5/GRCh38#179167816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50659994-C-A

179167925-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50659622-T-G

179168074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50659448-T-C

179168261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50659293-C-T

179168294-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50659262-C-G

179168314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50659243-C-T

179168330-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50659227-C-G

179168335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50659222-A-G

179168365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50659176-G-A

179168507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50659000-G-A

179168602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50658724-T-C

179168614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50658712-T-C

179168737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50658592-C-T

179168980-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50658396-G-C

179169054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50658367-A-G

179169145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50658285-G-A

179169371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50658099-T-C

179169409-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50658062-C-G

179169512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50657958-G-A

179169748-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50657768-C-G

179169851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50657680-G-A

179170046-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50657483-T-A

179170616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50656558-C-T

179170729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50656467-T-C

179170794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50656421-T-C

179170844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50656382-G-A

http://identifiers.org/hco/5/GRCh38#179171132-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50656116-C-A

179175358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50655173-A-G

179175898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50653993-G-A

179176207-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50653694-G-C

179176207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50653694-G-T

179176251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50653660-G-A

179176385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50653527-G-A

179176822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50652091-G-A

179176825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50652088-G-A

179176886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50652029-T-C

179180957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50647691-A-G

179181037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50647633-G-A

179181037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50647633-G-T

179181050-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50647620-C-G

179181050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50647620-C-T

179181133-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 50647543-T-G

179181199-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50647478-G-C

179181199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50647478-G-T

179181253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50647405-A-G

179181861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50646368-C-T

179181877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50646350-C-T

179181949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50646280-G-A

179181967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50646262-G-A

179182022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50646215-C-T

179182259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50645991-C-T

179182451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50645818-T-C

179182475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50645794-G-T

179182618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50645655-G-T

179182741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50645547-T-C

179182741-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50645547-T-G

179182801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50645484-G-A

179182905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50645381-G-A

179182912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50645375-G-A

179182953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50645340-C-T

179182967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50645326-T-C

179183170-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50645116-G-C

179183313-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50644934-C-G

179183319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50644928-G-A

179183510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50644717-G-A

179183510-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50644717-G-C

179183732-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50644505-G-C

http://identifiers.org/hco/5/GRCh38#179187099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50642725-C-A

179187287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50642553-C-T

http://identifiers.org/hco/5/GRCh38#179187604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#50642289-C-A

179187604-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 50642289-C-G

179187604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 50642289-C-T

179187766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 50642130-G-A

179187791-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50642104-C-G

179187858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50642038-T-C

179187867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50642029-G-A

179188036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50641885-G-A

179188036-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50641885-G-C

179188223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50641714-T-C

179188676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50641356-C-T

http://identifiers.org/hco/5/GRCh38#179188707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50641326-C-A

179188754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50641258-C-T

179188796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50641228-G-A

179188796-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50641228-G-C

179189007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50641022-T-C

179189072-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50640966-T-G

179189100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50640938-C-T

179190945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50639771-G-A

179190988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50639738-T-C

http://identifiers.org/hco/5/GRCh38#179191120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50639611-C-A

179191531-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50639335-G-C

179191589-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50639259-T-G

179191613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50639235-G-A

179191613-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50639235-G-C

http://identifiers.org/hco/5/GRCh38#179191874-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50638999-C-A

179191874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50638999-C-T

179193688-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50637861-G-C

179193695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50637854-T-C

179193900-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50637682-C-G

179193902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50637680-G-A

179194018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50637565-G-A

179194064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50637519-G-A

179194107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50637472-C-T

179194342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50637236-C-T

179194358-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50637218-C-G

179194358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50637218-C-T

179194414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50637158-G-A

179194414-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50637158-G-C

179195003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50637119-G-A

179195003-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50637119-G-C

179195290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50636833-G-A

179195418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50636697-G-A

http://identifiers.org/hco/5/GRCh38#179195445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50636671-C-A

179195493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50636623-C-T

http://identifiers.org/hco/5/GRCh38#179195494-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50636622-A-C

179195584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50636533-G-A

179195584-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50636533-G-C

http://identifiers.org/hco/5/GRCh38#179196334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50635784-C-A

179196334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50635784-C-T

179196492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50635667-C-T

179196508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50635651-C-T

179196549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50635610-G-A

179196549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50635610-G-T

179196573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50635586-G-A

179201048-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50634059-A-T

179201064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50634038-T-C

179201090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50634010-C-T

179201468-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50633657-C-G

179201468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50633657-C-T

179201870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50633576-T-C

179203337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50632966-C-T

179203451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50632856-C-T

http://identifiers.org/hco/5/GRCh38#179203532-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50632774-A-C

179203797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50632496-G-A

179203990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50632293-C-T

http://identifiers.org/hco/5/GRCh38#179204563-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50630728-A-C

179204563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50630728-A-G

179204698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50630634-T-C

179204759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50630568-G-A

http://identifiers.org/hco/5/GRCh38#179204799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50630542-C-A

179204810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50630533-G-A

179204839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50630503-C-T

179204958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50630380-T-C

179205086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50630231-G-A

179205122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50630186-G-A

179205147-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50630165-T-G

179205240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50630076-C-T

179205241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50630075-G-A

179205359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50629991-G-A

179205359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50629991-G-T

http://identifiers.org/hco/5/GRCh38#179205480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50629864-C-A

179205480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50629864-C-T

179205813-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50629575-T-A

179205813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50629575-T-C

179205814-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50629574-G-C

179205817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50629570-G-A

179205820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50629567-A-G

179206191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50629217-C-T

179206274-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50629133-C-G

179206360-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50629047-A-T

179207460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50628255-G-A

179207460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50628255-G-T

http://identifiers.org/hco/5/GRCh38#179207478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50628231-C-A

179207478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50628231-C-T

179207654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 50628052-G-A

179207769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50627900-A-G

http://identifiers.org/hco/5/GRCh38#179207791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50627860-C-A

179207791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50627860-C-T

http://identifiers.org/hco/5/GRCh38#179207808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50627843-C-A

179207808-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50627843-C-G

179207857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50627805-G-A

179207857-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50627805-G-C

179207857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50627805-G-T

179207874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50627788-G-A

179207914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50627770-A-G

179208059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50627674-C-T

179208172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50627606-G-A

179208172-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50627606-G-C

179208172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50627606-G-T

http://identifiers.org/hco/5/GRCh38#179208214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50627585-C-A

179208214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50627585-C-T

179208286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50627512-G-A

179208289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50627509-T-C

179208360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50627434-T-C

179209525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50625980-C-T

179209527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50625978-C-T

179209670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50625811-G-A

179209721-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50625753-G-C

179209722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50625752-G-A

179209735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50625740-G-A

179210104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50625356-G-A

179210560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50624847-C-T

179210570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50624734-C-T

179210683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50624502-G-A

179210723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50624480-C-T

179210784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50624428-A-G

179211559-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50623764-T-G

179211806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50623508-G-A

179211820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50623490-G-A

179211825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50623485-T-C

179211831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50623479-C-T

179212853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50622234-G-A

179213868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50620032-G-A

179213868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50620032-G-T

179213890-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50620010-T-A

179213891-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50620009-G-C

179214541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50619566-A-G

179214625-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50619478-C-G

179214689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50619416-T-C

179217585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50616524-T-C

179218607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50615519-C-T

http://identifiers.org/hco/5/GRCh38#179218608-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50615518-A-C

179218637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50615489-G-A

179218717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50615439-T-C

179218840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50615334-G-A

179218840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50615334-G-T

179218846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50615322-C-T

179218869-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50615292-C-G

179218871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50615290-C-T

179219605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50613770-G-A

179219769-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50613626-T-A

http://identifiers.org/hco/5/GRCh38#179219891-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50613558-A-C

179219965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50613488-G-A

179220000-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50613447-G-C

179220200-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50613253-T-G

179220297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50613156-G-A

179220719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50612808-C-T

179220879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50612703-T-C

179220989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50612618-C-T

179221776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50610443-A-G

179221794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50610420-C-T

179221805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50610409-G-A

179221904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50610337-G-A

179221904-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50610337-G-C

179222014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50610209-A-G

http://identifiers.org/hco/5/GRCh38#179222366-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50609829-A-C

179222554-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50609643-G-C

179222848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50609416-T-C

179223090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50609213-T-C

179223179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50609142-C-T

179223283-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50609088-T-A

179223283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50609088-T-C

179223389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50609012-C-T

179223448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50608974-A-G

http://identifiers.org/hco/5/GRCh38#179223578-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50608870-A-C

179223582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50608866-G-A

179224302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50608441-C-T

179224323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50608429-G-A

179224337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50608415-C-T

179224683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50608024-T-C

179227746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50606693-G-A

179227923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50606537-T-C

179228175-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50606320-G-T

179228183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50606308-G-A

179228272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50606265-A-G

179228393-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50606160-A-T

179228404-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50606149-T-G

179228407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50606148-T-C

179228525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50606024-G-A

179228525-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50606024-G-C

179228526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50606023-G-T

179228668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50605885-G-A

179228831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50605745-G-A

179228980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50605629-G-A

179228985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50605624-T-C

179229198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50605501-C-T

http://identifiers.org/hco/5/GRCh38#179229353-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50605422-C-A

179229353-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50605422-C-G

179229417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50605372-G-A

179229623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50605255-C-T

179230035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50604855-C-T

179230229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50604662-G-A

179230245-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50604641-G-C

179230246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50604640-G-A

179230261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50604625-G-A

179230272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50604599-A-G

179230494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50604327-T-C

179230524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50604296-A-G

179230549-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50604273-T-G

179232381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50601290-C-T

179232391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50601280-G-T

http://identifiers.org/hco/5/GRCh38#179232637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50601039-C-A

179232637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50601039-C-T

179235599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50599239-T-C

179235739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50599112-G-T

179235811-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50599051-T-A

179235878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50598990-C-T

179235921-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50598948-C-G

179236027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50598860-A-G

179236337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50598624-G-A

179236337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50598624-G-T

179242296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50589176-C-T

179242335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50589135-T-C

179242375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50589095-C-T

179242573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50588936-A-G

http://identifiers.org/hco/5/GRCh38#179242633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50588880-C-A

179250900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50582593-A-G

179250918-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50582575-G-C

179251009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50582489-G-A

179251009-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50582489-G-C

179251353-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50582207-A-T

179251436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50582122-G-A

179251532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50582030-C-T

179251993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50580358-T-C

179251993-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50580358-T-G

179252031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50580318-A-G

179252031-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50580318-A-T

179252034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50580315-G-A

179252034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50580315-G-T

179252053-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50580296-G-C

179252053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50580296-G-T

179252054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50580295-C-T

179252175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50580186-T-C

179252420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50579402-T-C

179252582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50579237-C-T

179252585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50579225-T-C

179252870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50578736-T-C

179253214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50578396-G-A

http://identifiers.org/hco/5/GRCh38#179253676-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50578242-A-C

179253841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50578144-C-T

http://identifiers.org/hco/5/GRCh38#179253861-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50578124-A-C

179255138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50575545-G-A

179255142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50575541-G-A

179255142-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50575541-G-C

179255219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50575475-T-C

179255452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50575218-T-C

http://identifiers.org/hco/5/GRCh38#179255776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50574851-C-A

179255784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50574844-A-G

179256050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50574544-C-T

179256060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50574534-G-A

179256374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50574248-C-T

179256441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50574197-C-T

179256490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50574148-T-C

179256571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50573982-G-A

179256625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50573923-G-A

179256706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50573868-G-A

179256706-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50573868-G-C

179256858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50573711-G-A

179256974-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50573570-C-G

179256974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50573570-C-T

179257131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50573443-G-A

179257349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50573205-G-A

179257462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50573085-C-T

179257532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50572946-T-C

179257559-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50572916-C-G

179257559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50572916-C-T

179257737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50572741-G-A

179257860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50572636-C-T

179258020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50572477-T-C

179258076-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50572422-G-C

179258165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50572321-G-A

179258349-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50572141-G-C

179258352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50572138-C-T

179258373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50572127-C-T

179258729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50571799-C-T

179258899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50571649-A-G

179259043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50571526-A-G

179259849-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 50570333-T-A

179259887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 50570295-G-A

http://identifiers.org/hco/5/GRCh38#179259979-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50570219-A-C

179259979-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 50570219-A-T

http://identifiers.org/hco/5/GRCh38#179260030-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50570168-A-C

179260035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 50570163-G-A

179260109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 50570074-A-G

179260321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 50569842-G-A

179260911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 50569361-G-A

179261220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 50569188-G-A

179261289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 50569121-G-A

179261345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 50569069-G-A

179261460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 50568967-C-T

179261461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 50568966-C-T

179263419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 50568412-T-C

179263432-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 50568398-T-A

179263432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 50568398-T-C

179263801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 50567434-C-T

179263990-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 50567244-A-T

179264031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 50567203-C-T

179264260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 50566943-C-T

179264865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 50566323-A-G

http://identifiers.org/hco/5/GRCh38#179264941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50566247-C-A

179265487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 50565706-G-A

179265498-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 50565695-C-G

http://identifiers.org/hco/5/GRCh38#179265565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50565642-C-A

179265565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 50565642-C-T

179265710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 50565488-C-T

179266484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 50564761-G-A

179266748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 50564518-G-A

179266759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 50564507-C-T

179266962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 50564281-T-C

179267055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 50564204-C-T

179267077-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 50564166-T-A

179267218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 50564022-G-T

179267628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 50563607-G-A

http://identifiers.org/hco/5/GRCh38#179268660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50562875-C-A

179268847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 50562822-G-A

179269230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 50562468-T-C

179270564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50561252-G-A

http://identifiers.org/hco/5/GRCh38#179270916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50560924-C-A

179271151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50560679-G-A

179271153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50560677-G-T

179271154-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50560676-T-G

179271231-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50560598-T-A

179271376-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50560413-G-C

179271531-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50560234-C-G

179271531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50560234-C-T

179271645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50560141-C-T

179271799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50559989-G-T

179271941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50559843-G-A

179271941-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50559843-G-C

179272023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50559777-G-A

179272023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50559777-G-T

179272136-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50559682-C-G

http://identifiers.org/hco/5/GRCh38#179272449-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50559381-A-C

179272623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50559253-C-T

179272653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50559223-G-A

179272741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50559163-G-A

http://identifiers.org/hco/5/GRCh38#179272762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50559138-C-A

179272762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50559138-C-T

http://identifiers.org/hco/5/GRCh38#179272778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50559122-C-A

179272778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50559122-C-T

179272813-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50559087-T-G

http://identifiers.org/hco/5/GRCh38#179272881-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50559004-A-C

http://identifiers.org/hco/5/GRCh38#179273048-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50558832-A-C

179273048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 50558832-A-G

179273048-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 50558832-A-T

179273101-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50558778-C-G

179273101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50558778-C-T

179273171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50558711-C-T

179273455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50558469-C-T

179273550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50558370-T-C

179274471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50557205-T-C

179274591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50557108-T-C

179274652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50557046-G-A

179274798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50556910-A-G

179274816-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50556894-G-C

179274824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50556878-G-T

179274962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50556745-A-G

179275278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50556602-G-A

179275341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50556565-G-T

179275347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50556559-G-A

179275347-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50556559-G-T

179275368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50556538-G-T

179275581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50556318-C-T

179275788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50556162-C-T

http://identifiers.org/hco/5/GRCh38#179275793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50556157-C-A

179275793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50556157-C-T

179276046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50555943-G-A

179276084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50555901-G-A

179276658-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50555315-A-T

179276907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50555098-C-T

179276921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50555084-G-A

179277130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50554729-G-T

179277237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50554609-C-T

179277381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50554513-G-A

179277398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50554496-G-T

http://identifiers.org/hco/5/GRCh38#179277415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50554484-C-A

179277415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50554484-C-T

http://identifiers.org/hco/5/GRCh38#179278098-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50553866-A-C

179278098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50553866-A-G

http://identifiers.org/hco/5/GRCh38#179278157-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50553827-A-C

http://identifiers.org/hco/5/GRCh38#179278173-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50553811-A-C

179278429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50553533-C-T

179278702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50553288-G-A

179278752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50553240-C-T

179278960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50553042-T-C

179279078-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50552931-T-G

179279961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50551514-C-T

179280016-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50551466-G-C

179280298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50551179-G-A

179280299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50551178-T-C

179280306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50551171-C-T

179280507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50551019-C-T

179280528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50551007-A-G

179280654-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50550855-A-T

179284769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50548355-C-T

179284863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50548284-G-A

179284951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50548197-G-A

179285268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50547934-T-C

179285283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50547919-A-G

http://identifiers.org/hco/5/GRCh38#179285479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50547459-C-A

179285514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50547435-G-A

179285771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50547174-G-A

179285771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50547174-G-T

179287291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50546210-C-T

179287346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50546154-C-T

179287461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50546056-G-A

179287461-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50546056-G-C

179287605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50545910-G-A

179287839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50545582-C-T

179287881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50545539-G-A

179288154-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50545334-G-C

179288279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50545221-C-T

179288337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50545161-C-T

179288486-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50545011-G-C

179288543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50544952-G-A

179288595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50544898-G-A

179293151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50541500-G-A

179293255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50541395-G-A

http://identifiers.org/hco/5/GRCh38#179293262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50541388-C-A

179293262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50541388-C-T

179293536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50541117-G-A

179297802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50539915-T-C

179298207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50539524-G-A

179298639-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50539056-T-G

179298958-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50538739-T-A

179299091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50538604-G-A

http://identifiers.org/hco/5/GRCh38#179299102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50538594-C-A

179299166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50538530-A-G

179299629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50538142-G-A

179299667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50538102-T-C

179300254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50537844-G-A

179300254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50537844-G-T

179300479-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50537652-T-A

179300479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50537652-T-C

http://identifiers.org/hco/5/GRCh38#179300613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50537522-C-A

http://identifiers.org/hco/5/GRCh38#179300927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50537217-C-A

179300927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50537217-C-T

179300946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50537198-A-G

179301188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50536956-C-T

179306799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50530281-G-A

179306803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50530277-A-G

179306803-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50530277-A-T

179306810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50530270-C-T

179306864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50530216-A-G

179307096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50529993-C-T

http://identifiers.org/hco/5/GRCh38#179307123-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50529959-A-C

179307123-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50529959-A-T

179307147-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50529935-C-G

179307160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50529919-G-A

179307516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50529593-G-A

179307516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50529593-G-T

179307543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50529565-T-C

179307557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50529551-G-A

179307635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50529471-C-T

179307836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50529275-C-T

179308138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50528281-G-A

179308138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50528281-G-T

179308395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50528036-G-A

http://identifiers.org/hco/5/GRCh38#179308674-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50527763-A-C

179308740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50527277-G-A

179308971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50527098-A-G

179309073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50526987-C-T

179309205-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50526872-A-T

179310864-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50526414-C-G

179310864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50526414-C-T

179310896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50526382-G-A

179310921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50526355-G-A

179310982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50526290-C-T

179310991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50526281-C-T

http://identifiers.org/hco/5/GRCh38#179311036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50526248-C-A

179311036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50526248-C-T

179311243-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50526048-G-C

179311529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50525774-C-T

179313943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50523694-C-T

179314049-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50523585-C-G

http://identifiers.org/hco/5/GRCh38#179314074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50523580-C-A

http://identifiers.org/hco/5/GRCh38#179314080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50523574-C-A

179314080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50523574-C-T

179314555-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50523087-C-G

179314555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50523087-C-T

179314605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50523027-T-C

179314667-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50522955-C-G

http://identifiers.org/hco/5/GRCh38#179314931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50522678-C-A

179314952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50522654-G-A

179314952-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50522654-G-C

179314984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50522625-C-T

179315040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50522588-C-T

179315227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50522391-G-A

179315440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50522250-G-A

179315672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50522066-G-A

179315732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50522002-C-T

http://identifiers.org/hco/5/GRCh38#179315866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50521888-C-A

179315878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50521876-G-A

179315909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50521844-G-T

179316039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50521699-C-T

179316178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50521543-G-A

179316207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50521517-G-T

179316396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50521372-G-A

179316456-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50521324-T-G

http://identifiers.org/hco/5/GRCh38#179316460-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50521320-A-C

http://identifiers.org/hco/5/GRCh38#179316493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50521287-C-A

179316568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50521211-G-A

179316584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50521195-A-G

179317173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50520899-G-T

179317216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50520856-C-T

179317262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50520810-C-T

179317415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50520670-C-T

179317718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 50520493-C-T

http://identifiers.org/hco/5/GRCh38#179318013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50520252-C-A

http://identifiers.org/hco/5/GRCh38#179318345-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50519895-A-C

179318527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50519690-G-A

179318691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50519564-C-T

179318703-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50519553-T-G

179318795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50519498-G-A

179319275-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50519121-C-G

179319419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50519072-G-A

179319675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50518951-C-T

http://identifiers.org/hco/5/GRCh38#179319704-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50518926-A-C

179319721-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50518909-T-A

179319730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50518900-T-C

179319735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50518895-G-A

179319749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50518884-C-T

179319800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50518840-C-T

179319910-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50518725-G-C

179320021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50518640-G-T

179320238-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50518395-A-T

179320648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50518085-G-T

179320668-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50518070-C-G

179320712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50518020-C-T

179320851-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50517868-T-G

179321298-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50516928-T-G

179321425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50516791-G-A

179321425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50516791-G-T

179321470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50516745-C-T

179321504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50516713-C-T

179321505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50516712-T-C

179321537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50516691-T-C

179321712-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50516579-T-G

179321763-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50516533-C-G

http://identifiers.org/hco/5/GRCh38#179321774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50516524-C-A

179321926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50516398-C-T

179322054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50516289-T-C

179322172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50516187-T-C

179322312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50516048-C-T

179322379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50515998-G-A

179322788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50515602-C-T

179322802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50515588-G-A

179322907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50515469-G-A

179323514-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50514965-G-C

179323514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50514965-G-T

179323567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50514931-T-C

179323678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50514878-G-A

179323678-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50514878-G-C

179325941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50513697-C-T

179326126-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50513500-T-G

http://identifiers.org/hco/5/GRCh38#179326238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50513415-C-A

179326238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50513415-C-T

179326634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50513041-A-G

179326996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50512687-G-A

179327190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50512500-T-C

179327246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50512439-A-G

179327760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50512245-C-T

179327871-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50512108-A-T

179327906-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50512081-T-A

179328300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50511987-G-A

http://identifiers.org/hco/5/GRCh38#179328308-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50511979-A-C

179328328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50511961-G-A

179328463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50511818-G-T

179328488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50511795-G-A

179328532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50511753-G-A

179328628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50511669-A-G

179328670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50511629-G-A

179328754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50511545-A-G

179328776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50511524-C-T

179328866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50511432-T-C

179329676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50510467-T-C

http://identifiers.org/hco/5/GRCh38#179329781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50510383-C-A

179329781-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50510383-C-G

179330312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50510208-G-A

http://identifiers.org/hco/5/GRCh38#179330352-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50510162-A-C

179330430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50510091-C-T

http://identifiers.org/hco/5/GRCh38#179330448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50510081-C-A

179330516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50510042-G-A

http://identifiers.org/hco/5/GRCh38#179330612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50509934-C-A

179330955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50509341-C-T

179331002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50509295-G-A

179331145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50509183-G-A

179331145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50509183-G-T

179331228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50509114-G-A

179331267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50509075-G-A

179331267-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50509075-G-C

179331290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50509039-A-G

179331494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50508868-A-G

179332133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50508404-C-T

179332479-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50508042-C-G

179333189-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50507382-G-T

179333549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50506743-A-G

179333551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50506741-G-T

179333914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50506692-G-A

179333954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50506655-T-C

179334039-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50506605-G-C

http://identifiers.org/hco/5/GRCh38#179334072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50506574-C-A

179334355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50506276-C-T

179334396-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50506244-G-C

179334566-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50506084-C-G

179335577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50504351-C-T

179335642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50504284-T-C

179336544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50502699-T-C

179336748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50502514-G-T

179336831-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50502449-C-G

179336974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50502307-G-A

http://identifiers.org/hco/5/GRCh38#179337332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50501960-C-A

179337600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50501712-G-A

179338099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50501356-C-T

179338254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50501180-G-A

179338254-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50501180-G-C

179338272-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50501170-C-G

http://identifiers.org/hco/5/GRCh38#179339332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50499626-C-A

179339508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50499468-G-A

179339508-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50499468-G-C

179339514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50499463-G-A

179339718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50499290-G-A

179339718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50499290-G-T

http://identifiers.org/hco/5/GRCh38#179340209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50498907-C-A

179340445-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50498650-G-C

179340540-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50498547-A-T

http://identifiers.org/hco/5/GRCh38#179340618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50498446-C-A

179340693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50498370-C-T

179340754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50498333-G-A

179340857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50498250-G-A

179340917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50498191-G-A

179340917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50498191-G-T

http://identifiers.org/hco/5/GRCh38#179341737-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50496298-A-C

179341737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50496298-A-G

179341862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50496185-G-A

179342526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50495592-A-G

179342861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50495259-G-T

179342928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50495196-T-C

179343196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50494939-T-C

179343253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50494898-C-T

179343268-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50494897-T-G

179343324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50494844-C-T

179343334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50494832-C-T

179343370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 50494812-A-G

179343439-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50494744-G-T

179343867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: 50494356-G-A

179343890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 50494333-C-T

179344017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: 50494206-G-A

179344017-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: 50494206-G-C

179344286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50493947-G-A

179344286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50493947-G-T

179344473-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50493798-G-C

179344749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50493542-T-C

http://identifiers.org/hco/5/GRCh38#179344880-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50493423-C-A

http://identifiers.org/hco/5/GRCh38#179345215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#50493099-C-A

179345215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, synonymous_variant, undefined
orthologous variants: 50493099-C-T

http://identifiers.org/hco/5/GRCh38#179345246-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50493068-A-C

179345246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 50493068-A-G

179345246-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 50493068-A-T

http://identifiers.org/hco/5/GRCh38#179345334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#50492983-C-A

179345334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 218
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 50492983-C-T