110347544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: non coding transcript exon variant
orthologous variants: 107232397-G-A

110348360-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107231657-T-A

http://identifiers.org/hco/1/GRCh38#110349107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107230643-C-A

110349107-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107230643-C-G

110349159-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107230573-G-C

110349304-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107230304-T-A

110349515-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107230119-C-G

110349540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107230098-T-C

110349697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107229945-T-C

110350271-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107229570-G-C

110350315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107229528-G-A

110350907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107228884-T-C

110351044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107228748-T-C

110351102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107228702-C-T

http://identifiers.org/hco/1/GRCh38#110352023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107227351-C-A

110352025-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107227349-T-G

110352429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107226846-A-G

110352429-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107226846-A-T

http://identifiers.org/hco/1/GRCh38#110353380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107226535-C-A

110353411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107226508-A-G

110353564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107226364-G-A

http://identifiers.org/hco/1/GRCh38#110353968-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107225607-A-C

110353968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107225607-A-G

110354341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107225311-G-A

110355431-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107224982-T-G

110355466-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107224942-C-G

110355466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107224942-C-T

110355473-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107224934-T-G

110355820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107224674-A-G

110356354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107224153-A-G

110357149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107223320-T-C

110361075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107221076-T-C

http://identifiers.org/hco/1/GRCh38#110362885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#107219397-C-A

110363244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107219087-T-C

http://identifiers.org/hco/1/GRCh38#110363953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#107218691-C-A

110363953-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107218691-C-G

110364935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107218084-G-T

110365414-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107217291-C-G

110370040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107215066-G-A

110370047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107215059-T-C

110370242-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107214893-T-A

http://identifiers.org/hco/1/GRCh38#110370298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#107214837-C-A

110370353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107214780-A-G

110370538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107214600-A-G

110370556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107214580-G-T

110370856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107214319-T-C

110370893-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107214280-T-A

110371646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107214141-C-T

110371816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107213998-G-A

110371816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107213998-G-T

110371822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107213988-G-T

110371845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107213968-G-T

110371881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107213932-G-A

110371881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107213932-G-T

110371957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107213870-C-T

110372129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107213683-T-C

110372697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107213088-G-A

110375490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107211786-C-T

110375573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107211702-G-T

110375578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107211697-C-T

110375646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107211625-A-G

110375646-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107211625-A-T

110375950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107211391-G-T

http://identifiers.org/hco/1/GRCh38#110375971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#107211373-C-A

110376130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107211208-G-A

110376212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107211115-A-G

110376221-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107211106-T-G

110376563-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107210906-G-C

110376840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107210684-A-G

110376850-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107210673-A-T

110376853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107210670-T-C

http://identifiers.org/hco/1/GRCh38#110376864-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#107210659-A-C

110376882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107210640-G-A

110376882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107210640-G-T

110376887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107210635-G-T

110376920-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107210613-T-A

110376928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107210608-G-A

110376928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107210608-G-T

http://identifiers.org/hco/1/GRCh38#110376972-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#107210564-A-C

110376972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107210564-A-G

110377164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 107210372-G-T

110377223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107210318-G-T

110377274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107210268-A-G

110377274-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107210268-A-T

110377556-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107210073-C-G

110377557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107210072-T-C

110377671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107209964-A-G

110378491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107208845-T-C

110378709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107208646-C-T

http://identifiers.org/hco/1/GRCh38#110378745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#107208614-C-A

110378745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107208614-C-T

110378815-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107208542-T-A

110378885-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107208502-A-T

110378927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107208460-G-A

110378987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107208400-G-A

110378987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107208400-G-T

110379002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107208385-G-A

110379051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107208327-C-T

110379069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107208309-A-G

110379191-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107208187-T-G

110379258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107208114-T-C

110379272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107208100-T-C

110379353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107208019-G-A

110379353-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107208019-G-C

110379353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107208019-G-T

http://identifiers.org/hco/1/GRCh38#110379682-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#107207819-A-C

110379682-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107207819-A-T

110380086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107207452-A-G

110380086-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107207452-A-T

110380106-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107207427-T-A

110380123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107207416-T-C

110380222-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107207323-T-G

110380351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107207189-G-A

110380351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107207189-G-T

110380537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107207019-A-G

110380835-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107206825-T-A

110380883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107206755-A-G

110380945-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107206631-T-A

http://identifiers.org/hco/1/GRCh38#110380981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#107206596-C-A

110380981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant, undefined
orthologous variants: 107206596-C-T

110381023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107206554-G-A

110381195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107206394-T-C

http://identifiers.org/hco/1/GRCh38#110381231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#107206363-C-A

110381231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107206363-C-T

110381666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107206279-A-G

110381687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107206258-A-G

110381743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107206202-A-G

110381744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107206201-A-G

110381768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107206177-A-G

110381841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107206108-G-A

110381841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107206108-G-T

110381845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107206104-C-T

110381906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107206045-G-T

110382159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107205933-A-G

110382174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107205919-T-C

110382520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107205690-A-G

110382604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107205609-T-C

http://identifiers.org/hco/1/GRCh38#110382666-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#107205563-A-C

110382821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107205404-G-A

110382959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107205266-A-G

110382971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 107205254-A-G

110382971-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 107205254-A-T

110383048-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107205191-T-G

110383132-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107205108-T-A

110386247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107203896-G-T

110386262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107203881-C-T

http://identifiers.org/hco/1/GRCh38#110386372-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#107203770-A-C

110386718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107203243-C-T

110386825-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107203138-G-C

110387416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107201641-A-G

110387513-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107201547-A-T

110387755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107201363-G-A

110387783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107201337-G-A

110387864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107201249-A-G

110388107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107201033-G-A

110388108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107201032-G-T

110388343-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107200773-G-C

http://identifiers.org/hco/1/GRCh38#110389094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#107199954-C-A

110389094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107199954-C-T

http://identifiers.org/hco/1/GRCh38#110389148-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#107199913-A-C

110389148-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107199913-A-T

110389150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107199911-G-A

110389150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107199911-G-T

110389169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107199895-G-T

110389184-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107199880-C-G

110389207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107199864-T-C

110389311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107199765-C-T

110389349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107199728-A-G

110389403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107199674-A-G

110390087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107199518-T-C

http://identifiers.org/hco/1/GRCh38#110390221-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#107199414-A-C

110390221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107199414-A-G

110390258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107199383-G-A

110390689-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107198980-G-C

http://identifiers.org/hco/1/GRCh38#110390729-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#107198927-C-A

110390848-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107198751-T-A

110391099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107198511-A-G

http://identifiers.org/hco/1/GRCh38#110391106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107198504-C-A

110391269-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107198361-C-G

110391486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107198058-C-T

110391602-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107197938-C-G

110391809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107197752-A-G

110391877-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107197688-A-T

110393442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107196909-T-C

110393486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107196863-G-A

110394420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107193975-T-C

110394555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107193893-T-C

110394792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107193707-A-G

110398431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107192640-A-G

110401185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107191473-A-G

110401274-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107191376-T-A

http://identifiers.org/hco/1/GRCh38#110401312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#107191338-C-A

110401312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107191338-C-T

110401414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107191118-G-T

110401488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107191045-T-C

110401488-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107191045-T-G

110401626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107190904-G-A

110401626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107190904-G-T

110401653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107190881-G-A

110401653-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107190881-G-C

110401653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107190881-G-T

110403904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107189355-C-T

110404045-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107189214-T-A

110404045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107189214-T-C

110404045-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107189214-T-G

http://identifiers.org/hco/1/GRCh38#110404120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107188667-C-A

110404125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107188662-G-A

110404152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107188644-T-C

110404303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107188539-A-G

110404420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107188409-G-A

110404812-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107187988-C-G

110404812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107187988-C-T

110404996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107187836-C-T

110405046-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107187794-T-A

110405046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107187794-T-C

110405943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107187560-G-A

110405983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107187524-G-A

110405983-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107187524-G-C

110406194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107187337-T-C

110406216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107187332-A-G

110406233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107187316-A-G

110406233-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107187316-A-T

110406452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107187111-G-A

110406452-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107187111-G-C

110406452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107187111-G-T

110406473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107187090-T-C

110406477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107187086-T-C

110406477-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107187086-T-G

110406927-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107186973-G-C

110406927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107186973-G-T

110406990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107186916-A-G

http://identifiers.org/hco/1/GRCh38#110407100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#107186809-C-A

110407100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107186809-C-T

http://identifiers.org/hco/1/GRCh38#110407176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#107186743-C-A

110407176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107186743-C-T

110407187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107186732-T-C

http://identifiers.org/hco/1/GRCh38#110407198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#107186721-C-A

110407198-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107186721-C-G

110407198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107186721-C-T

http://identifiers.org/hco/1/GRCh38#110407229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#107186680-C-A

110407229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107186680-C-T

110407313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107186610-G-A

110407313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107186610-G-T

http://identifiers.org/hco/1/GRCh38#110407391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#107186593-C-A

110407391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107186593-C-T

110407411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107186573-G-A

110407411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107186573-G-T

110407509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107186497-G-A

110407509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107186497-G-T

110407623-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107186390-C-G

110407623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107186390-C-T

110407674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107186339-C-T

110407750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107186263-G-A

110407750-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107186263-G-C

110407795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107186225-G-A

110407795-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107186225-G-C

110407802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107186218-A-G

110407803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107186217-G-A

110407925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107186151-A-G

http://identifiers.org/hco/1/GRCh38#110408013-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107186059-A-C

110408013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107186059-A-G

110408136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107185558-A-G

110408185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107185510-T-C

http://identifiers.org/hco/1/GRCh38#110408207-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107185486-A-C

110408211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107185400-C-T

110408217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107185394-T-C

http://identifiers.org/hco/1/GRCh38#110408236-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107185377-A-C

110408236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107185377-A-G

110408238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107185375-T-C

http://identifiers.org/hco/1/GRCh38#110408302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107185311-C-A

110408302-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107185311-C-G

110408302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107185311-C-T

http://identifiers.org/hco/1/GRCh38#110408622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107184998-C-A

110408638-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107184982-T-A

110408638-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107184982-T-G

110408684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107184937-T-C

http://identifiers.org/hco/1/GRCh38#110408920-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107184757-A-C

110409348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107184541-C-T

110409404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107184477-C-T

110409424-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107184456-T-G

http://identifiers.org/hco/1/GRCh38#110411419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107183023-C-A

110411419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107183023-C-T

110411452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107182994-G-T

110411510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107182948-G-T

110411523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 107182935-T-C

http://identifiers.org/hco/1/GRCh38#110411538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107182919-C-A

110411614-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107182859-T-A

110411614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107182859-T-C

http://identifiers.org/hco/1/GRCh38#110411627-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107182849-C-A

110411627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107182849-C-T

110411657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107182816-G-A

110411792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107182686-G-A

110411809-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107182669-T-A

http://identifiers.org/hco/1/GRCh38#110412264-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107181876-A-C

http://identifiers.org/hco/1/GRCh38#110412346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107181819-C-A

110412346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107181819-C-T

110412378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107181788-A-G

110412389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107181778-G-T

110412427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107181740-G-A

110412427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107181740-G-T

110412444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107181724-G-T

110412490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107181676-A-G

http://identifiers.org/hco/1/GRCh38#110412592-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#107181447-A-C

110412592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107181447-A-G

110412630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107181409-C-T

110412641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107181398-T-C

110412687-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107181356-G-T

110412865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107181139-G-T

110412887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107181117-C-T

110412946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107181061-G-T

110413777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107180421-T-C

110413837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107180367-G-T

110413859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107180346-G-T

110413866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107180339-C-T

110413867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107180338-A-G

110413973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107180084-G-T

110413978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107180079-C-T

110414066-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107179998-G-C

http://identifiers.org/hco/1/GRCh38#110414085-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107179979-A-C

110414098-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107179972-C-G

http://identifiers.org/hco/1/GRCh38#110414157-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107179901-A-C

110414221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107179729-T-C

110414263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107179687-C-T

110414353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107179604-G-A

110414353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107179604-G-T

110414431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107179531-C-T

http://identifiers.org/hco/1/GRCh38#110414555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107179405-C-A

110414706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107179265-A-G

110414882-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107179099-G-C

110414900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107179085-T-C

110414987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107178999-G-A

110414996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107178990-A-G

110415663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107178059-T-C

http://identifiers.org/hco/1/GRCh38#110416140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107177407-C-A

110416140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107177407-C-T

110416466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107177132-G-A

110416669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107176888-A-G

110419229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107174316-A-G

110419340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107174206-G-A

110420495-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107172053-T-G

110422702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107171625-A-G

110422953-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107171390-C-G

110424834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107169343-A-G

110425077-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107169098-T-G

http://identifiers.org/hco/1/GRCh38#110425162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107169028-C-A

110425162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107169028-C-T

http://identifiers.org/hco/1/GRCh38#110425172-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107169018-C-A

110425172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107169018-C-T

http://identifiers.org/hco/1/GRCh38#110425191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107169001-C-A

110425683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107168455-A-G

110425683-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107168455-A-T

110425749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107168384-C-T

http://identifiers.org/hco/1/GRCh38#110425763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107168370-C-A

110425763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107168370-C-T

http://identifiers.org/hco/1/GRCh38#110425808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107168325-C-A

110425808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107168325-C-T

http://identifiers.org/hco/1/GRCh38#110425820-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107168316-C-A

110425873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107168252-G-T

110425916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107168203-C-T

110425926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107168199-T-C

110425980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107168165-G-T

110426006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107168153-T-C

http://identifiers.org/hco/1/GRCh38#110426115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107168095-C-A

110426115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107168095-C-T

110426121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107168089-G-A

110426121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107168089-G-T

http://identifiers.org/hco/1/GRCh38#110426149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107168070-C-A

110426149-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107168070-C-G

110426149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107168070-C-T

110426166-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107168063-T-A

http://identifiers.org/hco/1/GRCh38#110426191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107168038-C-A

110426483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107167725-A-G

http://identifiers.org/hco/1/GRCh38#110426571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107167669-C-A

110426825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107167499-G-A

110426825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107167499-G-T

http://identifiers.org/hco/1/GRCh38#110426841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107167483-C-A

110426841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107167483-C-T

110426851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107167473-G-A

110426851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107167473-G-T

http://identifiers.org/hco/1/GRCh38#110426853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107167470-C-A

110426887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107167448-A-G

110426964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107167386-G-A

110426964-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107167386-G-C

http://identifiers.org/hco/1/GRCh38#110427134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107167228-C-A

110427160-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107167202-T-A

110427233-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107167129-T-G

110427416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107166973-G-A

110427671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107165746-C-T

110427716-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107165689-T-A

110427763-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107165633-T-G

110428994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107164388-G-A

110428994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107164388-G-T

110429060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107164315-G-A

110429069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107164306-G-T

110429098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107164278-A-G

http://identifiers.org/hco/1/GRCh38#110429133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107164244-C-A

110429133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107164244-C-T

110429773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107163932-C-T

http://identifiers.org/hco/1/GRCh38#110429779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107163923-C-A

110429779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107163923-C-T

110429789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 107163913-A-G

110429811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107163899-G-A

110429811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107163899-G-T

110429885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107163814-A-G

110429937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107163771-G-T

110430002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107163736-T-C

110430014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107163724-T-C

110430083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107163662-A-G

110430226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107163536-A-G

110430303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107163462-A-G

110430315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107163450-A-G

http://identifiers.org/hco/1/GRCh38#110430396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107163403-C-A

110430423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107163377-G-T

110430441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107163360-A-G

110430463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107163338-C-T

110430527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107163274-T-C

110430532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107163269-G-A

110430532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107163269-G-T

http://identifiers.org/hco/1/GRCh38#110430550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107163251-C-A

110430555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107163246-A-G

http://identifiers.org/hco/1/GRCh38#110430581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107163218-C-A

110430581-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107163218-C-G

110430581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107163218-C-T

110431556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107159410-T-C

110431598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107159368-T-C

110431601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107159365-A-G

http://identifiers.org/hco/1/GRCh38#110431618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107159350-C-A

110431618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107159350-C-T

110431644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107159324-T-C

http://identifiers.org/hco/1/GRCh38#110431645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107159323-C-A

110431685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107159290-C-T

110431705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107159270-T-C

http://identifiers.org/hco/1/GRCh38#110431726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107159249-C-A

110431745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107159232-T-C

110431813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107159025-A-G

http://identifiers.org/hco/1/GRCh38#110431859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107158968-C-A

110431871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107158956-A-G

110432035-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107158781-C-G

110432375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107158486-G-A

110432390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107158475-T-C

http://identifiers.org/hco/1/GRCh38#110432411-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107158454-A-C

110432452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107158417-A-G

110432526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107158346-A-G

110433631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107157795-G-A

110435577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107156429-A-G

110435592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107156408-G-A

110435592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107156408-G-T

110436428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107154509-C-T

http://identifiers.org/hco/1/GRCh38#110436529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107154404-C-A

110436529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107154404-C-T

110436675-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107154304-C-G

110442857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: non coding transcript exon variant
orthologous variants: 107153077-A-G

110442911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: non coding transcript exon variant
orthologous variants: 107153023-G-T

110442947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: non coding transcript exon variant
orthologous variants: 107152984-G-A

110442947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: non coding transcript exon variant
orthologous variants: 107152984-G-T

110443031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 107152904-G-A

110443031-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 107152904-G-C

110443031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 107152904-G-T

110443190-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107152754-G-C

110443358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107152605-A-G

110443420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107152553-G-T

http://identifiers.org/hco/1/GRCh38#110443562-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#107152428-A-C

110443562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107152428-A-G

110443579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 107152409-A-G

110443605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: non coding transcript exon variant
orthologous variants: 107152381-G-T

110443695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: non coding transcript exon variant
orthologous variants: 107152343-A-G

110443755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: non coding transcript exon variant
orthologous variants: 107152282-T-C

110443774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: non coding transcript exon variant
orthologous variants: 107152263-C-T

110443814-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40823
most severe consequence: non coding transcript exon variant
orthologous variants: 107152224-A-T