94146149-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103470985-C-G

94146149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103470985-C-T

http://identifiers.org/hco/14/GRCh38#94146152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#103470988-C-A

94146152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103470988-C-T

http://identifiers.org/hco/14/GRCh38#94146156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#103470992-C-A

94146156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103470992-C-T

94146232-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103471037-T-G

http://identifiers.org/hco/14/GRCh38#94146305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103471099-C-A

94146305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103471099-C-T

94146306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 103471100-A-G

94146346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103471140-T-C

94146444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103471236-T-C

94152658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103471464-G-A

94152658-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103471464-G-C

94152723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103471528-C-T

94152731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103471536-G-A

94152742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103471547-T-C

94153020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103471787-C-T

94153073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103471841-T-C

94153342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103471993-T-C

94156841-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103474275-T-G

94156913-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103474340-T-A

94156984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103474400-G-A

94156984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103474400-G-T

94157075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103474477-C-T

http://identifiers.org/hco/14/GRCh38#94157085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103474487-C-A

94157130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103474531-T-C

94157269-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 103474645-A-T

94157386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: 103474754-T-C

94157711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: 103475054-T-C

94157814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: 103475148-A-G

94157889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: 103475863-C-T

94157895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: 103475869-T-C

94158167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: 103476118-T-C

94158476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: 103476431-C-T

94163240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: 103478562-G-A

94163381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: 103478748-T-C

94163475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: 103478849-T-C

94163484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: 103478858-C-T

94163514-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: 103478897-A-T

http://identifiers.org/hco/14/GRCh38#94163733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103479723-C-A

94163744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: 103479734-G-T

94164016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: 103480002-G-A

94164068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: 103480049-T-C

94164236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: 103480175-C-T

94164622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: 103480496-C-T

94164963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: 103480870-A-G

94165117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: 103480985-A-G

http://identifiers.org/hco/14/GRCh38#94165211-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103481073-A-C

94165218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: 103481080-G-A

http://identifiers.org/hco/14/GRCh38#94165651-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103481425-C-A

94165651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: 103481425-C-T

94165767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: 103481506-C-T

94165883-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: 103481614-C-G

94165981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: 103481719-G-A

94166012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: 103481750-A-G

http://identifiers.org/hco/14/GRCh38#94166187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103481937-C-A

94166402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: 103482146-G-A

94166619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: 103482350-G-A

94166850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: 103482543-C-T

94166989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: 103482676-G-T

94167403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: 103483083-G-A

94167403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: 103483083-G-T

94167439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: 103483128-T-C

94167470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: 103483156-A-G

http://identifiers.org/hco/14/GRCh38#94167498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103483184-C-A

94167515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: 103483206-G-T

94167534-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: 103483216-G-T

94167535-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: 103483217-T-G

94167587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: 5 prime UTR variant
orthologous variants: 103483253-C-T

http://identifiers.org/hco/14/GRCh38#94167860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103483483-C-A

94167880-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: 103483491-T-G

94167954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: 103483553-G-A

94168053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: 103483631-C-T

94170287-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: 103490300-G-C

94170288-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: 103490301-G-C

94170388-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: 103490405-T-G

94170601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: 103490603-C-T

http://identifiers.org/hco/14/GRCh38#94171402-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103491763-A-C

94171728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: 103492069-C-T

94171800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: 103492142-A-G

http://identifiers.org/hco/14/GRCh38#94171965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103492277-C-A

94171965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: 103492277-C-T

94171971-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: 103492284-G-C

http://identifiers.org/hco/14/GRCh38#94172014-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103492329-A-C

94173417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: 103497887-C-T

http://identifiers.org/hco/14/GRCh38#94173515-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103497994-A-C

94173587-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: 103498047-C-G

94173603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: 103498061-G-A

94173678-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: 103498149-T-G

94173718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: 103498189-G-T

94173719-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: 103498190-C-G

94173719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: 103498190-C-T

94173749-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: 103498219-T-A

94173789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, undefined
orthologous variants: 103498262-T-C

94173848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: 103498321-C-T

94173911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: 103498378-C-T

94173919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: 103498385-A-G

94173967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: 103498434-G-A

94173967-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: 103498434-G-C

http://identifiers.org/hco/14/GRCh38#94174044-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#103498481-A-C

94174113-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: 103498550-G-C

94174113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: 103498550-G-T

94174178-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: 103498589-T-A

94174178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: 103498589-T-C

94174178-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: 103498589-T-G

94174195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: 103498604-G-A

94174195-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: 103498604-G-C

94174195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: 103498604-G-T

94174257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, undefined
orthologous variants: 103498665-G-A

94174257-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, undefined
orthologous variants: 103498665-G-C

94174257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, undefined
orthologous variants: 103498665-G-T

94174309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: 103498712-G-A

94174309-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron variant
orthologous variants: 103498712-G-T

94174313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 103498721-G-A

94174313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 103498721-G-T

http://identifiers.org/hco/14/GRCh38#94174483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103498896-C-A

94174483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 103498896-C-T

94174484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 103498897-G-A

http://identifiers.org/hco/14/GRCh38#94174727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103499142-C-A

94174727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103499142-C-T

http://identifiers.org/hco/14/GRCh38#94174772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103499171-C-A

94174966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103499351-T-C

94174966-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103499351-T-G

94174989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103499368-G-A

94175003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103499392-A-G

94175334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103499697-T-C

94175334-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103499697-T-G

94175394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103499757-G-A

94175394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103499757-G-T

94175412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103499770-G-A

94175412-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103499770-G-C

94175412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103499770-G-T

94175413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103499771-G-A

94175413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103499771-G-T

94175455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103499817-A-G

94175468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103499836-G-A

94175468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103499836-G-T

94175473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103499841-C-T

94175503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103499872-G-A

94175503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103499872-G-T

http://identifiers.org/hco/14/GRCh38#94175579-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103499915-A-C

94175579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103499915-A-G

94175701-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103500016-A-T

94175813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103500128-G-T

94175919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103500215-T-C

94176092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 103500368-C-T

94176361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103500649-G-A

94176424-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103500712-G-C

94176782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103501145-G-T

94176952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103501334-G-A

94177088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103501480-C-T

94177594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103501992-C-T

94177952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103502337-C-T

94178062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103502446-C-T

94178299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103503269-C-T

94178508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103503614-T-C

94178571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103503643-G-A

94178683-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103503754-C-G

94178865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103503940-C-T

94179038-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103504116-C-G

94179044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103504122-C-T

94179061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103504139-G-T

94179181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103504254-C-T

94179371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103504437-G-T

94179404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103504462-A-G

94179716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103505348-G-A

94182360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103505682-C-T

94182429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103505752-T-C

94182475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103505791-A-G

94182526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103505966-G-A

94182575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103506033-T-C

94183049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103506488-C-T

94183532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103507037-G-A

94183651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103507152-G-A

94184238-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103507621-C-G

94184707-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103507790-G-C

94184774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103507853-A-G

94184775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103507854-T-C

94184815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103507908-C-T

94185668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103508442-G-T

94185718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103508492-C-T

94185887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103508637-A-G

94185934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103508673-A-G

94186257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103509008-C-T

94186446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103509164-A-G

94186464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103509182-G-A

http://identifiers.org/hco/14/GRCh38#94189198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103513780-C-A

94189198-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103513780-C-G

94189405-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103516391-C-G

94189434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103516421-T-C

94189675-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103516690-A-T

94189779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103516784-C-T

94189886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103516869-T-C

http://identifiers.org/hco/14/GRCh38#94189907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103516889-C-A

94190689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103517201-T-C

94191135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103517622-G-T

94191256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103517732-A-G

http://identifiers.org/hco/14/GRCh38#94192094-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103518414-A-C

94192183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103518478-G-A

94192183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103518478-G-T

94192203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103518501-T-C

http://identifiers.org/hco/14/GRCh38#94192208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103518506-C-A

94192459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103518776-A-G

94192595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103518909-A-G

94192666-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103518977-T-G

94192683-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103518994-C-G

http://identifiers.org/hco/14/GRCh38#94192759-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103519066-A-C

94192859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103519169-G-T

94193314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103520134-T-C

94193451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103520257-G-A

94193468-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103520274-G-C

94193724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103520515-T-C

94193860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103520632-A-G

94193863-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103520635-T-A

94194568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103521221-G-A

94194568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103521221-G-T

94206890-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103522980-T-A

94207217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103523214-A-G

94207752-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103523977-G-C

94208311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103524503-A-G

http://identifiers.org/hco/14/GRCh38#94208382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103524558-C-A

94208423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103524586-G-T

94208465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 103524628-G-A

94208465-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 103524628-G-C

94208644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103524813-G-A

94208644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103524813-G-T

94208785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103524917-G-A

94208989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103525124-T-C

94209316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103525455-G-T

94209402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103525538-A-G

http://identifiers.org/hco/14/GRCh38#94209497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103525611-C-A

94209511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103525628-A-G

94209646-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103525732-C-G

94209719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103525805-C-T

94210789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103527118-C-T

94210806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103527139-A-G

94211480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103527743-G-A

94211511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103527768-G-A

94211592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103527844-G-A

94211651-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103527884-T-A

94211788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103528031-G-A

94211958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103528213-A-G

94212062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103528287-C-T

94212764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103529286-G-T

94212774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103529297-G-A

94212836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103529351-A-G

94212921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103529441-G-T

94213157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103529669-C-T

94213558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103530019-G-A

94213585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103530045-T-C

94213592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103530052-G-A

94213619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103530081-C-T

94213775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103530175-G-A

http://identifiers.org/hco/14/GRCh38#94213783-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103530181-A-C

94214603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103531899-A-G

94214605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103531901-A-G

94214723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103532020-A-G

94215194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103532112-T-C

94215247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103532146-G-A

http://identifiers.org/hco/14/GRCh38#94215425-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103532316-A-C

94215425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103532316-A-G

94215658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103532605-T-C

94215701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103532654-A-G

94215945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103533029-T-C

94216024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103533137-C-T

94216175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103533243-A-G

94216453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103533534-C-T

94216655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103533698-C-T

94216782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103533816-C-T

94225853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103538174-G-T

94226379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103538607-A-G

94226383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103538611-C-T

94226388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103538616-T-C

94226447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103538669-A-G

94226467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103538685-C-T

94226522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103538737-T-C

http://identifiers.org/hco/14/GRCh38#94226615-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103538817-A-C

94226929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103539044-A-G

94227015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103539113-G-A

http://identifiers.org/hco/14/GRCh38#94227139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103539201-C-A

94227139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103539201-C-T

94227146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103539208-T-C

http://identifiers.org/hco/14/GRCh38#94227162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103539219-C-A

94227162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103539219-C-T

http://identifiers.org/hco/14/GRCh38#94227194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103539251-C-A

94227194-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103539251-C-G

94227194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103539251-C-T

http://identifiers.org/hco/14/GRCh38#94227198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103539255-C-A

94227198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103539255-C-T

94227204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103539261-A-G

http://identifiers.org/hco/14/GRCh38#94227233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103539290-C-A

94227233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103539290-C-T

94227370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 103539411-C-T

94227478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 103539527-C-T

94227487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 103539536-G-A

94227581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103539627-G-T

http://identifiers.org/hco/14/GRCh38#94227605-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103539651-A-C

94227605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 103539651-A-G

94227667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103539709-T-C

94227759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103539790-G-T

94227816-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103539831-T-G

94227863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103539876-A-G

94227884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103540046-A-G

94227925-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103540087-T-G

http://identifiers.org/hco/14/GRCh38#94227950-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103540112-A-C

94227950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103540112-A-G

94227955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103540118-G-A

94227955-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103540118-G-C

94227955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103540118-G-T

94227968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103540133-G-A

94227968-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103540133-G-C

94227968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103540133-G-T

94227969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103540134-A-G

94227969-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103540134-A-T

http://identifiers.org/hco/14/GRCh38#94227973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103540138-C-A

94228031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103540186-C-T

94228943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103540381-A-G

94229043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103540480-T-C

94229764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103541367-A-G

http://identifiers.org/hco/14/GRCh38#94229843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103541454-C-A

94229929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103541521-G-T

94230074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103541655-C-T

94230511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103542466-A-G

94230761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103542712-A-G

94230767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103542716-G-T

94230955-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103542832-T-A

94231090-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103542948-T-A

94231090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103542948-T-C

94231110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103542967-A-G

94231177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103543028-G-A

94231188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103543039-A-G

94231490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103543315-T-C

94232298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103544286-A-G

94232416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103544393-A-G

94233245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103544883-T-C

94233248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103544886-A-G

94233373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103544987-A-G

94233536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103545135-G-A

94233536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103545135-G-T

http://identifiers.org/hco/14/GRCh38#94233548-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103545147-C-A

94233548-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103545147-C-G

94233548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103545147-C-T

http://identifiers.org/hco/14/GRCh38#94233566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103545164-C-A

94233658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 103545256-G-A

94233802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103545398-G-A

94233802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103545398-G-T

94233892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103545480-G-A

94233892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103545480-G-T

94233985-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103545569-A-T

http://identifiers.org/hco/14/GRCh38#94234679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103547755-C-A

94234730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103547846-T-C

http://identifiers.org/hco/14/GRCh38#94234766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103547883-C-A

94234766-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103547883-C-G

94234923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103548034-G-A

94236867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103549560-T-C

94237122-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103549793-A-T

94237145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103549823-G-A

94237173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103549850-A-G

94237173-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103549850-A-T

94237290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103549962-G-A

94237301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103549977-A-G

94237510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103550261-T-C

94237595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 103550345-T-C

94237814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103550548-T-C

http://identifiers.org/hco/14/GRCh38#94237819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103550552-C-A

http://identifiers.org/hco/14/GRCh38#94237835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103550568-C-A

94238352-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103550627-C-G

94238691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103551009-G-A

94238701-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103551019-T-A

94239877-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103551209-A-T

http://identifiers.org/hco/14/GRCh38#94240104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103551423-C-A

94240240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103551563-A-G

94240266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103551599-A-G

94240375-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103551709-T-G

http://identifiers.org/hco/14/GRCh38#94240567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103551862-C-A

94240567-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103551862-C-G

94240567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103551862-C-T

94240577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103551872-A-G

94240577-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103551872-A-T

http://identifiers.org/hco/14/GRCh38#94240584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103551879-C-A

94240584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103551879-C-T

94240610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103551904-T-C

94240655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103551948-T-C

http://identifiers.org/hco/14/GRCh38#94240811-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103552099-A-C

94240811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103552099-A-G

94240820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103552108-A-G

http://identifiers.org/hco/14/GRCh38#94240855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103552142-C-A

94240855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103552142-C-T

94240914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103552173-A-G

94241107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103552348-G-A

94241107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103552348-G-T

http://identifiers.org/hco/14/GRCh38#94241334-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103552611-A-C

94241354-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103552631-G-C

94241555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103552810-A-G

94241616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103553034-A-G

94241633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103553051-C-T

94241636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103553054-A-G

http://identifiers.org/hco/14/GRCh38#94241638-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103553056-A-C

94241638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103553056-A-G

94241638-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103553056-A-T

94241648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103553067-T-C

94241649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103553068-G-A

94241709-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103553130-T-G

94241752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103553174-T-C

94241931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 103553353-C-T

94241945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 103553367-T-C

94241961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103553383-A-G

94241981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103553404-A-G

94242138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103553557-A-G

http://identifiers.org/hco/14/GRCh38#94242209-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103553624-A-C

94242209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103553624-A-G

94242212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103553627-G-A

http://identifiers.org/hco/14/GRCh38#94242325-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103553732-A-C

94242325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 103553732-A-G

94242325-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 103553732-A-T

94242336-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 103553743-T-G

94242382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 103553789-T-C

http://identifiers.org/hco/14/GRCh38#94242415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103553822-C-A

94242471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103553872-G-A

94242471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103553872-G-T

94242669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103554076-T-C

94242727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103554106-A-G

94242790-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103554167-C-G

94242859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103554244-A-G

94243036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103555149-T-C

94243158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103555301-T-C

94243298-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103555803-A-T

94243690-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103556151-C-G

94244026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103556468-A-G

94244343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103556770-C-T

94244382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103556806-G-T

94244614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103557017-G-A

94244614-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103557017-G-C

94244614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103557017-G-T

94244706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 103557109-A-G

94244706-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 103557109-A-T

94244931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103557251-T-C

94245070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103557381-C-T

94245085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103557396-A-G

94245372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103557624-G-T

94245382-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103557634-C-G

94245485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103557689-G-A

http://identifiers.org/hco/14/GRCh38#94245486-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103557690-A-C

94245486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103557690-A-G

94245530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103557730-T-C

94245677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 103557876-T-C

94245677-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 103557876-T-G

94245755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103557948-G-T

94245797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103558778-G-A

94245797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103558778-G-T

94245816-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103558793-A-T

94245878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103558852-G-A

94246057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103558959-A-G

94246632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103559521-C-T

http://identifiers.org/hco/14/GRCh38#94246651-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103559536-C-A

94246651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103559536-C-T

94246679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103559564-A-G

94246922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103559972-C-T

94247184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103560306-A-G

94249277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103561550-A-G

94249546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103561799-T-C

94249800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103562200-G-A

94249811-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103562235-A-T

94249962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103562440-C-T

94250007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103562487-T-C

94250046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103562525-G-A

94250046-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103562525-G-C

94250351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103562816-T-C

94250352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103562817-G-A

94250389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103562887-T-C

http://identifiers.org/hco/14/GRCh38#94250826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103563300-C-A

94250867-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103563342-C-G

94250867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103563342-C-T

94250902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103563382-A-G

94250947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103563408-G-A

94250980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103563442-A-G

http://identifiers.org/hco/14/GRCh38#94250984-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103563446-A-C

94251047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103563508-T-C

94251047-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103563508-T-G

94251643-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103564257-A-T

94251695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103564309-T-C

94251977-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103564608-T-A

94251977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103564608-T-C

94252042-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103564702-T-A

94254162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103564905-C-T

94254642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103565293-T-C

94254696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103565347-T-C

94254893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103565520-C-T

94255038-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103565613-C-G

http://identifiers.org/hco/14/GRCh38#94255537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103565886-C-A

94255537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103565886-C-T

94255674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103565938-G-A

94255713-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103565967-C-G

94256101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103566324-T-C

94256309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103566484-T-C

94256313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103566488-G-T

94256385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103566560-A-G

94256404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103566583-T-C

94256404-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103566583-T-G

94256418-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103566597-A-T

94256419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103566598-G-T

http://identifiers.org/hco/14/GRCh38#94256613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103566776-C-A

94256613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103566776-C-T

94256640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103566801-G-A

94256640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103566801-G-T

94256668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103566829-A-G

http://identifiers.org/hco/14/GRCh38#94256669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103566830-C-A

94256669-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103566830-C-G

94256676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103566837-A-G

94256717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103566860-G-T

94256787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103566926-G-A

94256787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103566926-G-T

94256797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103566941-A-G

94256895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103567037-T-C

94256961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103567089-A-G

94257062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103567182-A-G

94257198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103567301-T-C

94257312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103567412-T-C

94258717-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103567552-T-A

94259234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103567688-T-C

http://identifiers.org/hco/14/GRCh38#94259259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103567711-C-A

94259272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103567724-A-G

94259309-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 103567761-T-A

94259309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 103567761-T-C

94259309-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 103567761-T-G

http://identifiers.org/hco/14/GRCh38#94259407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103567852-C-A

94259490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103567931-T-C

94259541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103567993-A-G

94264501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103568637-A-G

94264626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103568776-A-G

http://identifiers.org/hco/14/GRCh38#94264756-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103568910-A-C

94264804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103569142-G-A

94264804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103569142-G-T

94264845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103569180-T-C

94265043-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103569907-G-C

94265111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103569973-G-T

94265154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103570039-G-A

94265154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103570039-G-T

http://identifiers.org/hco/14/GRCh38#94265372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103570216-C-A

http://identifiers.org/hco/14/GRCh38#94265591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103571023-C-A

http://identifiers.org/hco/14/GRCh38#94265870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103571302-C-A

94265870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 103571302-C-T

94265918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103571346-A-G

http://identifiers.org/hco/14/GRCh38#94265939-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103571369-A-C

http://identifiers.org/hco/14/GRCh38#94265941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103571371-C-A

94266002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103571428-G-A

94266002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103571428-G-T

94266026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103571447-T-C

94266040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103571461-T-C

94266164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103571580-T-C

94266165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103571581-A-G

94266178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103571593-A-G

94266692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103572638-A-G

94266692-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103572638-A-T

http://identifiers.org/hco/14/GRCh38#94266836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103572984-C-A

94266863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103573066-G-A

94266863-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103573066-G-C

94266989-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 103573190-T-G

94267077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103573272-T-C

94267175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103573369-A-G

94267238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103574011-G-A

94267286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103574057-A-G

94267299-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103574070-T-G

94267786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103574462-C-T

94274822-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103576273-C-G

94274822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103576273-C-T

http://identifiers.org/hco/14/GRCh38#94274873-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103576324-A-C

94274900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103576349-A-G

94274930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103576374-G-A

http://identifiers.org/hco/14/GRCh38#94275022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103576453-C-A

94275105-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103576533-G-C

94275137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103576574-G-A

94275336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103576762-A-G

94275386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 103576804-G-A

http://identifiers.org/hco/14/GRCh38#94275579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103576987-C-A

94275579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103576987-C-T

94277308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103577941-A-G

94277428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103578064-C-T

94277858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103578397-G-A

94277858-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103578397-G-C

94277858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103578397-G-T

94277893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103578435-C-T

94277995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103578501-C-T

94278235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103578728-G-A

94278317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103578802-A-G

94278317-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103578802-A-T

94278511-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103578970-T-A

94278601-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103579049-A-T

94278663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 103579111-A-G

94278689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 103579131-A-G

94278850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 103579263-A-G

http://identifiers.org/hco/14/GRCh38#94278881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103579285-C-A

http://identifiers.org/hco/14/GRCh38#94279037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103579428-C-A

http://identifiers.org/hco/14/GRCh38#94279060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#103579457-C-A

94279060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 103579457-C-T

94279082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 103579479-G-T

94279529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 103579888-C-T