110888402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: non coding transcript exon variant
orthologous variants: 46444695-G-T

110888444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: non coding transcript exon variant
orthologous variants: 46444653-T-C

110888448-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: non coding transcript exon variant
orthologous variants: 46444649-C-G

110895121-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46443937-G-C

110895121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46443937-G-T

110895181-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46443875-T-G

110895216-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46443841-T-G

110895283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46443818-A-G

110895437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46443680-C-T

110897072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46441038-A-G

110897334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46440733-C-T

110897446-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46440617-A-T

http://identifiers.org/hco/3/GRCh38#110897847-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#46440215-A-C

110898104-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46439987-T-A

110899432-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46439909-G-C

110899503-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46439827-A-T

110899555-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46439785-T-G

110899684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46439276-C-T

110899848-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46439162-G-C

110899849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46439161-A-G

110900243-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46438725-T-G

110900369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46438599-C-T

110901019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46437978-G-A

http://identifiers.org/hco/3/GRCh38#110901031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#46437966-C-A

110901031-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46437966-C-G

110901036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46437961-C-T

110901127-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46437872-T-G

110901316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46437698-T-C

110901327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46437684-T-C

110901378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46437633-T-C

110901389-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46437622-C-G

110901657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46436651-C-T

110901728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46436586-A-G

110901772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46436544-T-C

110901851-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46436466-A-T

110901935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46436353-T-C

http://identifiers.org/hco/3/GRCh38#110902228-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#46435875-C-A

110902326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46435837-C-T

110902826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46435334-C-T

110903015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46435227-G-A

110903748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46434247-T-C

110903936-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46434037-G-C

110903947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46434021-G-T

110904087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46433881-C-T

110904128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46433840-T-C

http://identifiers.org/hco/3/GRCh38#110904275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#46433709-C-A

110905860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46432451-G-A

110906238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46432152-C-T

110906430-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46431971-C-G

110906585-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46431831-C-G

110906653-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46431773-C-G

110906705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46431721-G-A

110906847-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46431594-C-G

110906847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46431594-C-T

110907083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46431360-A-G

110907260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46431196-A-G

110907292-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46431165-T-A

110907519-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46429906-C-G

110907736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46429711-A-G

110907745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46429702-G-A

110907831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46429619-C-T

110907859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46429617-G-A

110908300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46428442-T-C

http://identifiers.org/hco/3/GRCh38#110908362-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#46427980-C-A

110908464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46427878-C-T

110908545-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46427799-G-C

110909141-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46427247-G-C

110909232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46427147-A-G

http://identifiers.org/hco/3/GRCh38#110909255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#46427120-C-A

110909340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46427040-A-G

http://identifiers.org/hco/3/GRCh38#110909383-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#46426987-A-C

110909383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46426987-A-G

110909870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46426239-G-A

110909875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46426234-T-C

110910137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46426002-T-C

110910216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46425921-C-T

110910251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46425886-T-C

110910386-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46425749-C-G

110910647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46425482-T-C

http://identifiers.org/hco/3/GRCh38#110911069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#46425051-C-A

http://identifiers.org/hco/3/GRCh38#110911157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#46424986-C-A

110911157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46424986-C-T

http://identifiers.org/hco/3/GRCh38#110911233-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#46424911-A-C

110917712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46424530-A-G

110917801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46424458-C-T

110917844-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46424427-T-A

110918198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46424030-C-T

110918203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46424028-C-T

110918206-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46424025-T-A

110918296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46423939-C-T

110918328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46423917-A-G

110918381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46423867-T-C

http://identifiers.org/hco/3/GRCh38#110918410-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#46423831-A-C

http://identifiers.org/hco/3/GRCh38#110918451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#46423753-C-A

110918451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46423753-C-T

110918518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46423682-T-C

110918523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46423677-T-C

110918822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46423455-A-G

110919193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46423105-A-G

110919359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46422935-T-C

110919921-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46422349-T-A

110919921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46422349-T-C

110920094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46422171-T-C

110920363-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46421883-T-A

110920365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46421881-C-T

110920619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46421623-G-A

110920744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46421507-C-T

110920810-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46421446-G-C

110920956-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46421329-C-G

110921023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46421263-T-C

110921121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46421164-G-A

110921490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46420822-T-C

110921505-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46420807-G-C

110921552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46420761-T-C

110921636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46420686-T-C

110921640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46420682-T-C

110921709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46420625-G-T

110921848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46420484-C-T

110921994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46420351-A-G

110922151-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46420196-G-C

110922278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46418964-A-G

http://identifiers.org/hco/3/GRCh38#110922336-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#46418906-A-C

110922336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46418906-A-G

110922360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46418882-A-G

110922362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46418880-G-A

http://identifiers.org/hco/3/GRCh38#110922666-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#46418719-C-A

110922887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46418523-G-A

110922921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46418469-C-T

110923162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46415352-T-C

110923251-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46415262-T-G

110923448-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46415093-T-A

110923674-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46414893-T-A

110923674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46414893-T-C

110923687-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46414880-A-T

110923815-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46414727-C-G

110923815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46414727-C-T

http://identifiers.org/hco/3/GRCh38#110924053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#46414591-C-A

110924247-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46414424-T-G

110924258-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46414414-C-G

110924393-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46414266-T-A

110924489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46414170-G-A

110924493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46414166-C-T

http://identifiers.org/hco/3/GRCh38#110924546-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#46414111-A-C

110925237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46413737-G-A

110925475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46413701-G-A

http://identifiers.org/hco/3/GRCh38#110925658-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#46413517-A-C

110925658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46413517-A-G

110925764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46413403-G-A

110925834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46413334-C-T

110925975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46413179-A-G

110926074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46412889-C-T

http://identifiers.org/hco/3/GRCh38#110926107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#46412868-C-A

110926241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46412754-G-A

110926241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46412754-G-T

110926519-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46412486-T-A

110926585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46412420-C-T

http://identifiers.org/hco/3/GRCh38#110926659-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#46412334-A-C

110926740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46412266-T-C

110927269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46411835-G-A

http://identifiers.org/hco/3/GRCh38#110927626-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#46411242-A-C

110927641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46411222-T-C

110927763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46411110-G-A

110927763-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46411110-G-C

110927904-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46410999-T-G

110928750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46410515-G-T

110928775-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46410489-A-T

110928785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46410479-G-A

110928934-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46410353-T-G

110928996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46410300-A-G

110929454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46409125-T-C

110929798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46408169-A-G

110929912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46408056-C-T

110929926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46408042-T-C

http://identifiers.org/hco/3/GRCh38#110930028-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#46407965-C-A

110930544-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46407341-A-T

110930839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46407083-A-G

110930857-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46407064-T-G

110930859-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46407062-T-A

110930976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46406975-T-C

110931006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46406946-G-T

110931039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46406914-G-A

110931040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46406913-G-A

110931040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46406913-G-T

110931128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46406810-T-C

110931133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46406805-C-T

110931260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46406736-T-C

110931359-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46406656-G-C

110931450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46406565-G-A

110931452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46406563-C-T

110931495-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46406516-A-T

110932297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46405520-C-T

110932519-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 46405335-A-T

110932579-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 46405275-T-G

110932588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 46405266-G-A

110932588-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 46405266-G-C

110932831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 46405023-T-C

110933185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46404619-A-G

110935399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46403174-A-G

110935419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46403156-A-G

110935429-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46403146-C-G

110935429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46403146-C-T

110935643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46402955-C-T

110935763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46402839-A-G

110935943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46402644-T-C

110936061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46402517-T-C

http://identifiers.org/hco/3/GRCh38#110936281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#46402304-C-A

110936281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46402304-C-T

110936345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46402239-T-C

110936727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46401999-G-A

110936940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46401813-T-C

110937252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46401491-T-C

110937356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46401384-T-C

110937356-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46401384-T-G

110937490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46401255-C-T

110937514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46401236-T-C

110937532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46401218-C-T

110937585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46401161-A-G

http://identifiers.org/hco/3/GRCh38#110937586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#46401160-C-A

110937864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46400891-C-T

110938284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46400452-C-T

http://identifiers.org/hco/3/GRCh38#110938508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#46400093-C-A

110938709-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46399895-A-T

110938805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46399001-C-T

110939318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46397144-T-C

110939472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46396981-T-C

110939493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46396960-A-G

110939603-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46396868-G-C

110939869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46396625-A-G

110940118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46396396-C-T

110940133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46396381-G-A

110940596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46395859-C-T

110940716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46395735-A-G

110941743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46394196-T-C

110954369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46393446-A-G

110954387-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46393425-C-G

110954387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46393425-C-T

110954401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46393411-A-G

110954503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46393337-T-C

110956017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46387068-A-G

110956099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46386984-C-T

110956175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46386916-C-T

110956285-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46386816-T-A

110956290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46386811-G-T

110956361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46386753-A-G

http://identifiers.org/hco/3/GRCh38#110956576-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#46386577-A-C

110957034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46386157-G-T

110957041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46386150-C-T

110957591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46385134-T-C

110957781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46384942-C-T

http://identifiers.org/hco/3/GRCh38#110959711-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#46383779-A-C

110959894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46383594-T-C

110960002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46383493-C-T

110960227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46383311-A-G

110971773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46377925-A-G

110972255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46377455-G-A

http://identifiers.org/hco/3/GRCh38#110972368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#46377310-C-A

110972481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46377213-G-A

110972574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46377095-C-T

110972603-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46377066-T-A

110972635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46377039-G-A

110972641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46377033-T-C

110972671-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46377010-T-A

110972711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46376971-C-T

http://identifiers.org/hco/3/GRCh38#110972926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#46376567-C-A

110973357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46376067-T-C

110973368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46376056-A-G

110973384-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46376040-T-A

110973384-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46376040-T-G

110973493-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46375936-T-G

110973548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46375878-G-A

110974438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46374327-G-A

110974658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46374032-A-G

110974672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46374018-T-C

http://identifiers.org/hco/3/GRCh38#110974710-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#46373980-A-C

110974795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46373895-T-C

http://identifiers.org/hco/3/GRCh38#110974796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#46373894-C-A

110975108-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46373578-T-A

110975335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46373349-T-C

110976239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46372037-C-T

110976245-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46372031-T-A

110980886-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46370042-T-A

110981338-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46369598-T-G

110981463-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46369475-C-G

110981580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46369356-C-T

110981680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46369286-G-A

110981847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46369190-T-C

110982195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46368887-G-T

110982634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46368504-C-T

110982762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46368396-G-A

110982762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46368396-G-T

110983012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46367819-C-T

110983128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46367704-T-C

110983271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46367582-C-T

110983281-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46367572-A-T

110992197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46367145-A-G

110992271-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46367064-T-A

110992513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46366560-T-C

110993299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46365799-A-G

110993847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46365268-A-G

110993852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46365263-G-A

110993885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46365230-T-C

110993943-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46365178-T-A

110994031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46365095-T-C

110994081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46365046-G-A

http://identifiers.org/hco/3/GRCh38#110994254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#46364883-C-A

110994358-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46364781-G-C

110994365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46364775-G-A

110994803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46363864-G-T

110994899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46363760-C-T

110995282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46363274-T-C

110995351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46363206-A-G

110995352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46363205-T-C

110995425-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46363109-T-G

http://identifiers.org/hco/3/GRCh38#110995446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#46363088-C-A

http://identifiers.org/hco/3/GRCh38#110995487-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#46362953-A-C

110995869-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46362511-A-T

110996188-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46362199-T-A

110996412-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46361971-T-G

110997166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46360785-T-C

110997166-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46360785-T-G

http://identifiers.org/hco/3/GRCh38#110997208-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#46360736-A-C

110997208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46360736-A-G

110997627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46360375-T-C

110997706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46360292-T-C

110997714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46360287-A-G

110997757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46360280-C-T

110998201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46357919-T-C

111004775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46357671-A-G

111004818-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46357647-A-T

111004832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46357632-C-T

111004977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46357023-T-C

111005215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46356895-T-C

111005425-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46356727-G-C

111005439-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46356713-A-T

http://identifiers.org/hco/3/GRCh38#111006518-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#46355741-A-C

111006606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46355653-G-A

111006606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46355653-G-T

http://identifiers.org/hco/3/GRCh38#111006625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#46355641-C-A

111006625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46355641-C-T

111006629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46355637-T-C

111006649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46355617-T-C

111006680-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 46355581-G-C

111006680-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 46355581-G-T

111007059-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46353917-T-G

111007628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46353351-A-G

111007701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46353271-G-T

111009040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46351056-T-C

http://identifiers.org/hco/3/GRCh38#111009093-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#46351002-C-A

111009093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46351002-C-T

111009130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46350963-G-A

111009130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46350963-G-T

111009717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46349238-C-T

111011115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46349238-C-T

http://identifiers.org/hco/3/GRCh38#111011233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#46349130-C-A

111011375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46348988-T-C

http://identifiers.org/hco/3/GRCh38#111011376-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#46348987-A-C

111011376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46348987-A-G

111011407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46348956-T-C

111011525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46348772-A-G

111011617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46348690-C-T

111011691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46348631-C-T

111011860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46348472-C-T

http://identifiers.org/hco/3/GRCh38#111011869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#46348452-C-A

111011910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46348411-T-C

111012279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46348059-A-G

111012446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46347893-A-G

111012636-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46347755-T-A

111012725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46347671-T-C

111012796-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46347599-C-G

http://identifiers.org/hco/3/GRCh38#111012868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#46347527-C-A

111012929-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46347466-G-C

111013028-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 46347399-G-C

111013274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46347161-T-C

111014755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46346790-G-A

http://identifiers.org/hco/3/GRCh38#111014777-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#46346769-A-C

111015596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46346025-C-T

111015643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46345971-T-C

111015657-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46345957-G-C

111015721-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46345896-T-A

111015721-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46345896-T-G

http://identifiers.org/hco/3/GRCh38#111015975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#46345595-C-A

111015975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46345595-C-T

111016088-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46345296-G-C

111016147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46345241-G-A

http://identifiers.org/hco/3/GRCh38#111016162-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#46345230-A-C

111016162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46345230-A-G

111016162-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46345230-A-T

111016178-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46345214-C-G

111016315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46345088-C-T

http://identifiers.org/hco/3/GRCh38#111016775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#46344931-C-A

111016829-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46344893-C-G

111016983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46344744-T-C

http://identifiers.org/hco/3/GRCh38#111017323-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#46344473-A-C

111031826-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46343006-T-A

111032092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46342746-A-G

111032205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46342640-C-T

111032353-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46342471-C-G

111032360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46342461-T-C

111032411-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46342409-T-A

111032505-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46342318-C-G

111032622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46342142-C-T

111032646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46342119-T-C

111034233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46341831-T-C

111034233-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46341831-T-G

111034303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46341748-A-G

111034394-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46341689-G-C

111034431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46341655-G-A

111034431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46341655-G-T

http://identifiers.org/hco/3/GRCh38#111034802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#46341335-C-A

111034835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46341310-T-C

111034839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46341306-A-G

111034980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46340900-G-A

111035029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46340851-C-T

111044866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46340735-A-G

111044880-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46340721-T-G

111044926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46340675-T-C

111045081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46340527-A-G

111045123-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46340490-T-A

111045285-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46340332-G-C

111045286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46340331-A-G

111045861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46340214-G-A

111045941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46340135-C-T

111046134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46339986-C-T

111046436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46339787-C-T

111046515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46339699-G-A

111046786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46339452-G-T

111046996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46339267-G-A

111047020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46339242-T-C

111047347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46338884-T-C

111047561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46338684-G-T

111047597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46338649-T-C

111047841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46338411-T-C

111047905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46338342-T-C

111048157-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46338083-T-A

111048691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46336114-T-C

111048752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46336068-T-C

111048813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46336019-G-A

111048813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46336019-G-T

111048924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46335919-T-C

111052525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46330536-T-C

http://identifiers.org/hco/3/GRCh38#111052533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#46330527-C-A

111052533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46330527-C-T

111052538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46330522-G-A

111052592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46330311-T-C

http://identifiers.org/hco/3/GRCh38#111052621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#46330282-C-A

http://identifiers.org/hco/3/GRCh38#111052808-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#46330029-A-C

111052808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46330029-A-G

111053986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46329494-C-T

111054065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46329387-A-G

111054611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46329067-T-C

http://identifiers.org/hco/3/GRCh38#111055439-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#46328747-A-C

111055439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46328747-A-G

111055628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46328552-A-G

111055954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46328234-T-C

111056016-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46328169-A-T

111056226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46327941-T-C

111056303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46327878-T-C

111063637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46326962-A-G

111063667-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46326925-A-T

111063771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46326834-T-C

111063980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46326704-T-C

111063980-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46326704-T-G

111064139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46326491-C-T

111064193-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46326406-A-T

111066058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46322786-T-C

111066156-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46322676-A-T

111066232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46322588-C-T

111066279-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46322529-T-G

111066439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46322362-G-A

111066519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46322287-A-G

111066841-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46321958-T-A

111067041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46321784-C-T

http://identifiers.org/hco/3/GRCh38#111067089-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#46321749-A-C

111067460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46321484-C-T

111067477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46321467-C-T

111068191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46320735-G-A

111068191-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46320735-G-C

111068207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46320723-T-C

111068223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46320708-A-G

http://identifiers.org/hco/3/GRCh38#111068786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#46320224-C-A

111069304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46319765-C-T

111069507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46319519-T-C

111069508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46319518-A-G

111069550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46319476-C-T

111070124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 46318915-T-C

111070387-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46318695-G-C

111070387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46318695-G-T

http://identifiers.org/hco/3/GRCh38#111070429-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#46318652-A-C

http://identifiers.org/hco/3/GRCh38#111070809-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#46318296-A-C

111070811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46318294-G-T

111070883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46318228-G-A

111070883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46318228-G-T

http://identifiers.org/hco/3/GRCh38#111070941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#46318162-C-A

111070941-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46318162-C-G

111070941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46318162-C-T

111070975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46318128-T-C

111071002-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46318096-T-A

111071002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46318096-T-C

111071018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46318080-C-T

http://identifiers.org/hco/3/GRCh38#111071031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#46318067-C-A

111071031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46318067-C-T

111071064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46318034-A-G

111071066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46318032-G-A

111071066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46318032-G-T

111071067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46318029-T-C

http://identifiers.org/hco/3/GRCh38#111071070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#46318026-C-A

http://identifiers.org/hco/3/GRCh38#111071178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#46317959-C-A

111071178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46317959-C-T

http://identifiers.org/hco/3/GRCh38#111071240-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#46317894-A-C

111071240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46317894-A-G

111071331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46317804-G-A

111071344-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46317791-G-C

111071344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46317791-G-T

111071345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46317790-G-A

111071345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46317790-G-T

111071351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46317784-G-A

111071381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46317743-T-C

111071381-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46317743-T-G

http://identifiers.org/hco/3/GRCh38#111071470-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40813
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#46317655-A-C