132721847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103880510-C-T

132721848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103880509-T-C

132721903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103880455-G-T

http://identifiers.org/hco/3/GRCh38#132721939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#103880381-C-A

132721939-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103880381-C-G

132721939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103880381-C-T

132721943-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103880377-G-C

132721943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103880377-G-T

132721946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103880375-G-A

132721957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103880364-C-T

132722078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 103880243-C-T

http://identifiers.org/hco/3/GRCh38#132722213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#103880120-C-A

http://identifiers.org/hco/3/GRCh38#132722214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#103880119-C-A

132722214-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 103880119-C-G

132722249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: 103880084-G-A

132722249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: 103880084-G-T

132722310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 103880023-T-C

132722385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103879940-T-C

132722385-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103879940-T-G

132722421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103879892-G-A

132722421-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103879892-G-C

132722421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103879892-G-T

132722487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103879801-G-A

132722487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103879801-G-T

132722502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103879784-G-A

132722502-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103879784-G-C

132722502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103879784-G-T

132722541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103879747-G-A

132722541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103879747-G-T

132722544-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103879744-C-G

132722544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103879744-C-T

132722595-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103879687-G-C

132722882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103879368-G-A

132723137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103879073-C-T

132723411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103878840-C-T

132724280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103876411-T-C

132724355-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103876337-G-C

132724570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103875626-T-C

132724850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103875386-C-T

132724919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103875316-T-C

132725117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103875136-C-T

132725683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103874596-G-A

132725743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103874534-A-G

132725983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103874322-C-T

http://identifiers.org/hco/3/GRCh38#132726484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#103873942-C-A

132726484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103873942-C-T

http://identifiers.org/hco/3/GRCh38#132726487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#103873939-C-A

132726487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103873939-C-T

132726732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103873694-A-G

132726825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103873599-G-T

132726840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103873584-A-G

132727101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103873287-C-T

132727482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103872734-T-C

132727540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: non coding transcript exon variant
orthologous variants: 103872676-A-G

132727701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103872542-T-C

132727708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103872535-A-G

132727740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103872504-C-T

132728049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103872263-T-C

132728067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103872245-G-T

132728595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103872046-A-G

132728595-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103872046-A-T

132729098-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103863211-C-G

132729098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103863211-C-T

132729482-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103862806-A-T

132729817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103862537-T-C

http://identifiers.org/hco/3/GRCh38#132729823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103862531-C-A

132729945-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103862400-T-A

http://identifiers.org/hco/3/GRCh38#132730129-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103862360-A-C

132730203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103862290-T-C

http://identifiers.org/hco/3/GRCh38#132730252-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103862246-A-C

132738375-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103859916-T-G

132738419-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103859871-C-G

132740031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103858946-C-T

132740259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103858724-C-T

132740299-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103858684-T-A

132740380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103858604-A-G

132740422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103858563-G-A

132740436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103858549-T-C

132740517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103858469-T-C

132740538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103858459-A-G

132747906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103856847-C-T

132747954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103856783-G-T

132748117-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103856613-T-A

132748209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103856545-T-C

132748388-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103856370-T-A

132748762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103855807-A-G

132748874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103855701-G-T

132748992-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103855598-A-T

132749106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103855488-T-C

132749330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103855262-G-T

132749489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103855165-G-A

132749489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103855165-G-T

132749538-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103855102-A-T

132749544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103855096-C-T

http://identifiers.org/hco/3/GRCh38#132749599-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103855042-C-A

132749599-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103855042-C-G

http://identifiers.org/hco/3/GRCh38#132749620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103855020-C-A

132749631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103855009-A-G

http://identifiers.org/hco/3/GRCh38#132749634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103855006-C-A

132749634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103855006-C-T

132749693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103854952-C-T

http://identifiers.org/hco/3/GRCh38#132750399-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103849374-A-C

132750399-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103849374-A-T

132750408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103849365-C-T

132750440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103849335-G-A

132750440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103849335-G-T

http://identifiers.org/hco/3/GRCh38#132750457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103849318-C-A

132750601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103849177-A-G

132750601-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103849177-A-T

132750823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103848967-G-T

132750830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103848960-G-A

132750879-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103848911-T-A

132750924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103848866-A-G

132751035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103848660-G-T

132751444-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103848274-A-T

132751570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103848153-T-C

132752741-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103846356-C-G

132752805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103846292-G-A

132752805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103846292-G-T

132753107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103846020-T-C

132753110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103846017-A-G

132753125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103846014-C-T

132753492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103844695-G-T

http://identifiers.org/hco/3/GRCh38#132753611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103844596-C-A

132753765-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103844455-G-C

132754150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103844093-A-G

132754500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103843758-G-A

http://identifiers.org/hco/3/GRCh38#132754587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103843698-C-A

132755297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103839484-A-G

132755487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103839164-A-G

132755572-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103839070-C-G

http://identifiers.org/hco/3/GRCh38#132755643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103839010-C-A

132755945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103838746-T-C

132757770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103835778-A-G

132758725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103835335-T-C

132758775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103835286-T-C

132758874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103835029-T-C

132758909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103834995-A-G

http://identifiers.org/hco/3/GRCh38#132759099-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103834811-A-C

132772329-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103832986-C-G

132772416-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103832912-C-G

132772553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103832776-G-A

132772985-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103832349-C-G

132774646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103831034-T-C

132774690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103830990-T-C

132774943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103830620-T-C

132775060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103830441-C-T

132775096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103830405-A-G

132775412-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103830084-T-A

132783120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103829426-G-A

132783120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103829426-G-T

132783212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103829344-G-A

132783385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103829175-A-G

132783392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103829168-T-C

132783408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103829153-A-G

132783443-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103829118-C-G

132783570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103828999-A-G

132783582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103828987-A-G

132783634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103828964-C-T

132783704-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103828882-T-G

132783780-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103828788-T-G

132783832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103828736-G-T

132783927-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103828641-C-G

132783952-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103828618-T-G

132784078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103828526-T-C

132787765-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103828390-T-G

132787847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103828308-G-T

132787942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103828225-C-T

132787977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103828208-G-A

132788386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103827577-G-A

http://identifiers.org/hco/3/GRCh38#132795533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103825674-C-A

132799597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103825333-G-A

132799597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103825333-G-T

http://identifiers.org/hco/3/GRCh38#132799638-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103825292-A-C

132799638-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103825292-A-T

132799995-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103824005-C-G

132804253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103823717-C-T

132804954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103823051-T-C

132813360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103819098-T-C

132813376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103819082-A-G

132813574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103818915-G-A

http://identifiers.org/hco/3/GRCh38#132813869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103818633-C-A

132813869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103818633-C-T

132814043-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103818457-T-G

132814211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103818300-G-A

132814278-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103818233-G-C

132814482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103818022-A-G

132814816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103817595-G-T

132814933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103817475-C-T

132815115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103817329-A-G

132815154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103817302-C-T

132815155-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103817301-A-T

132816319-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103816077-C-G

132816319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103816077-C-T

132816491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103815914-G-A

132816491-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103815914-G-C

132816624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103815772-T-C

132816713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: non coding transcript exon variant
orthologous variants: 103815651-G-T

132816765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: non coding transcript exon variant
orthologous variants: 103815628-G-A

132816765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: non coding transcript exon variant
orthologous variants: 103815628-G-T

132816870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: non coding transcript exon variant
orthologous variants: 103815546-A-G

132816879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: non coding transcript exon variant
orthologous variants: 103815537-T-C

132816888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: non coding transcript exon variant
orthologous variants: 103815528-A-G

http://identifiers.org/hco/3/GRCh38#132816909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103815514-C-A

132816909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: non coding transcript exon variant
orthologous variants: 103815514-C-T

http://identifiers.org/hco/3/GRCh38#132816941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103815483-C-A

132816960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: non coding transcript exon variant
orthologous variants: 103815464-G-A

132816960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: non coding transcript exon variant
orthologous variants: 103815464-G-T

132817021-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103815416-C-G

132817095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103815334-T-C

132817104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103815325-T-C

132817146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103815232-T-C

132817190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103815196-C-T

132817522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103814875-G-T

132817578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103814843-G-A

132817688-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103814754-C-G

132817925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103814528-A-G

132818109-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103814410-C-G

132818144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103814374-T-C

132818206-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103814321-T-A

132818260-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103814269-T-G

132818317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103814219-C-T

132818476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: non coding transcript exon variant
orthologous variants: 103814075-G-T

132818504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: non coding transcript exon variant
orthologous variants: 103814043-G-T

132818507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: non coding transcript exon variant
orthologous variants: 103814038-T-C

132818526-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: non coding transcript exon variant
orthologous variants: 103814019-G-C

132818558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: non coding transcript exon variant
orthologous variants: 103813994-G-A

132818558-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: non coding transcript exon variant
orthologous variants: 103813994-G-C

http://identifiers.org/hco/3/GRCh38#132818821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103813725-C-A

132818897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: non coding transcript exon variant
orthologous variants: 103813660-C-T

132818898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: non coding transcript exon variant
orthologous variants: 103813659-A-G

132818949-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: non coding transcript exon variant
orthologous variants: 103813606-A-T

132818957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: non coding transcript exon variant
orthologous variants: 103813598-G-A

http://identifiers.org/hco/3/GRCh38#132818985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103813558-C-A

132819019-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: non coding transcript exon variant
orthologous variants: 103813529-T-A

132819019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: non coding transcript exon variant
orthologous variants: 103813529-T-C

132819054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: non coding transcript exon variant
orthologous variants: 103813485-G-A

132822740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103809182-A-G

132822829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103809095-A-G

132822908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103809015-T-C

132823001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103808919-C-T

132823231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103808712-G-A

132823353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103808614-A-G

132823491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103808471-C-T

132823495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103808467-C-T

132823553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103808407-C-T

132823815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103808201-A-G

132823860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103808155-G-A

132823860-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103808155-G-C

132823860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103808155-G-T

132824212-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103807822-T-A

http://identifiers.org/hco/3/GRCh38#132824270-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103807762-A-C

132824297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103807728-C-T

132824550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103807168-G-A

132824818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103806518-T-C

132824991-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103806350-C-G

132827257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103804984-C-T

132827295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103804946-G-A

132827627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103803382-T-C

132828033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103802501-G-A

132828033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103802501-G-T

132828046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103802488-T-C

http://identifiers.org/hco/3/GRCh38#132828116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103802413-C-A

132828140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103802393-G-T

132828162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103802378-G-A

132828314-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103802272-G-C

132828887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103801336-G-A

132829382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103800724-C-T

http://identifiers.org/hco/3/GRCh38#132829413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103800706-C-A

http://identifiers.org/hco/3/GRCh38#132829425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103800694-C-A

132829425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103800694-C-T

132829426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103800693-A-G

132829673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103800357-G-A

132829744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103800295-C-T

132830693-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103799575-T-G

132830721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103799547-A-G

132830758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103799510-A-G

132830805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103799464-C-T

132830831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103799438-A-G

132830861-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103799405-T-A

http://identifiers.org/hco/3/GRCh38#132832029-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103797667-A-C

132832135-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103797562-G-C

132832285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103797426-A-G

http://identifiers.org/hco/3/GRCh38#132832294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103797418-C-A

132832440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103797279-A-G

132832542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103797183-A-G

132832622-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103797108-T-A

132832623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103797107-G-A

http://identifiers.org/hco/3/GRCh38#132832656-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103797075-A-C

132832727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103797007-A-G

132833249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103796870-G-A

132834026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103794315-G-A

132834026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103794315-G-T

http://identifiers.org/hco/3/GRCh38#132834632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103793693-C-A

132834632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103793693-C-T

132834909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103793388-G-A

132835157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103793123-T-C

http://identifiers.org/hco/3/GRCh38#132835210-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103793074-A-C

132835255-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103793030-T-A

132835283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103793025-G-A

132835290-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103793018-T-A

132835290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103793018-T-C

http://identifiers.org/hco/3/GRCh38#132835310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103793010-C-A

132835311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103793009-A-G

132835517-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103792854-G-C

132835609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103792779-C-T

132835639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103792748-G-T

132835727-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103792660-T-A

132835727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103792660-T-C

132836140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103792399-G-A

132836158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103792382-G-A

132836203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103792338-G-A

132836386-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103791962-C-G

132837633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103789762-G-A

132837674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103789715-A-G

http://identifiers.org/hco/3/GRCh38#132838203-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103789182-A-C

132838265-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103789140-A-T

132838305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103789100-T-C

132838591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103788849-C-T

132838731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103788732-C-T

132838749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103788714-G-A

132839479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103787519-T-C

132839711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103787265-G-A

132839895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103787121-A-G

132840245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103786868-T-C

132840257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103786856-A-G

132840298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103786815-A-G

132840364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103786755-T-C

132840505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103786617-G-A

132840631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103786511-G-A

132840669-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103786472-C-G

132840678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103786463-C-T

132840963-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103786193-C-G

132840963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103786193-C-T

132841344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103785821-G-A

132841381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103785764-T-C

132841463-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103785492-G-C

132841850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103785067-T-C

132842000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103784916-G-A

132842004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103784912-C-T

132842124-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103784783-G-C

http://identifiers.org/hco/3/GRCh38#132842168-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103784724-A-C

132842258-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103784623-T-G

132842373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103784170-A-G

132845722-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103782501-T-A

132845722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103782501-T-C

132845782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103782440-G-A

http://identifiers.org/hco/3/GRCh38#132845826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103782395-C-A

http://identifiers.org/hco/3/GRCh38#132845969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103782273-C-A

http://identifiers.org/hco/3/GRCh38#132846006-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103782232-A-C

132847971-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103781345-G-C

132848009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103781303-G-T

132848249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103781074-C-T

132848562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103780786-T-C

http://identifiers.org/hco/3/GRCh38#132848614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103780734-C-A

132848798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103780543-G-A

132865704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103779237-A-G

132865739-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103779208-A-T

132865792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103779158-A-G

132865872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103779090-C-T

132866332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103778688-A-G

http://identifiers.org/hco/3/GRCh38#132866496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103778515-C-A

132866522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103778486-C-T

http://identifiers.org/hco/3/GRCh38#132866616-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103778403-A-C

132867708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103777522-G-A

http://identifiers.org/hco/3/GRCh38#132867835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103777366-C-A

132867874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103777325-T-C

132867903-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103777293-T-G

132867939-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103777262-G-C

http://identifiers.org/hco/3/GRCh38#132867962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103777242-C-A

132868017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103777204-G-A

132868085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103777160-A-G

132873907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: non coding transcript exon variant
orthologous variants: 103776623-A-G

http://identifiers.org/hco/3/GRCh38#132873944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103776588-C-A

http://identifiers.org/hco/3/GRCh38#132874020-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#103776532-A-C

132874071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24129
most severe consequence: non coding transcript exon variant
orthologous variants: 103776483-A-G