112308192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: non coding transcript exon variant
orthologous variants: 55187130-G-A

112308192-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: non coding transcript exon variant
orthologous variants: 55187130-G-C

112308225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 55187164-T-C

112308279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: 55187218-G-A

112308286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 55187225-G-T

112308296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55187235-G-A

112308296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55187235-G-T

112308366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55187272-G-T

112308425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55187332-G-A

112308425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55187332-G-T

112308489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55187367-G-A

112308551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55187429-A-G

112308740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55187591-G-A

http://identifiers.org/hco/10/GRCh38#112308913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55187713-C-A

112308918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55187718-G-A

112308918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55187718-G-T

112309091-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55187788-G-C

112309091-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55187788-G-T

112309128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55187816-T-C

http://identifiers.org/hco/10/GRCh38#112309236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55187923-C-A

112309236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: non coding transcript exon variant
orthologous variants: 55187923-C-T

112309271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: non coding transcript exon variant
orthologous variants: 55187958-C-T

112309328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55188015-A-G

112309398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55188081-T-C

112309586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55188517-G-A

112310291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55189731-T-C

112310748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55190133-G-T

112310971-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55190339-T-G

http://identifiers.org/hco/10/GRCh38#112311069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55190439-C-A

112311113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55190480-A-G

112311256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 55190628-A-G

http://identifiers.org/hco/10/GRCh38#112311273-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55190645-A-C

112311273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55190645-A-G

112311273-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55190645-A-T

112311274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55190646-G-A

112311274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55190646-G-T

http://identifiers.org/hco/10/GRCh38#112311277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55190649-C-A

112311277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55190649-C-T

112311361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55190746-T-C

112311370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55190755-G-T

112311395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55190776-C-T

112311536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55190922-T-C

112311628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55190988-G-A

112311740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55191039-G-A

112311820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55191117-G-T

http://identifiers.org/hco/10/GRCh38#112311821-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55191118-A-C

112311821-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55191118-A-T

112311942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55191178-G-A

112311943-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55191179-T-A

112312221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55191359-T-C

112312254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55191392-A-G

112312297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55191423-A-G

http://identifiers.org/hco/10/GRCh38#112312333-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55191459-A-C

112312423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: non coding transcript exon variant
orthologous variants: 55191549-C-T

112312441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: non coding transcript exon variant
orthologous variants: 55191567-G-A

112312441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: non coding transcript exon variant
orthologous variants: 55191567-G-T

http://identifiers.org/hco/10/GRCh38#112312498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55191625-C-A

http://identifiers.org/hco/10/GRCh38#112312513-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55191640-A-C

112312513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55191640-A-G

http://identifiers.org/hco/10/GRCh38#112312514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55191641-C-A

112312514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55191641-C-T

112312532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55191659-G-A

112312532-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55191659-G-C

112312546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55191679-G-A

112312546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55191679-G-T

112312578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55191713-T-C

112312580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55191715-C-T

112312597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55191731-A-G

http://identifiers.org/hco/10/GRCh38#112312619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55191753-C-A

112312651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55191784-C-T

112312741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55191853-T-C

http://identifiers.org/hco/10/GRCh38#112312767-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55191878-A-C

112312864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55191975-A-G

112312883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55192013-A-G

112312933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55192084-T-C

112313321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55192451-G-T

112313442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55192555-G-T

112313485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55192590-C-T

112313606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55192726-C-T

http://identifiers.org/hco/10/GRCh38#112313634-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55192757-A-C

112314095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55194467-G-A

112314130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55194502-T-C

112314250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 55194585-T-C

112314399-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: non coding transcript exon variant
orthologous variants: 55194734-T-A

112314542-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55194882-G-C

112314574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55194913-A-G

112314599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55194937-C-T

112315119-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55195454-A-T

112315208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55195693-T-C

112315447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 55196441-A-G

http://identifiers.org/hco/10/GRCh38#112315671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55196627-C-A

112315756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55196686-C-T

112315785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55196716-G-A

112315811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55196739-G-A

112315824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55196752-C-T

112315831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55196758-C-T

112315943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55196872-G-A

112315946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55196875-T-C

112316061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55196988-G-A

112316626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55197507-C-T

112316657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55197554-C-T

112316662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55197559-G-A

112316680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55197582-G-A

112317278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55198158-G-T

112317282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55198162-T-C

112317401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55198268-T-C

112317440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55198307-G-A

112317503-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55198379-T-A

112317503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55198379-T-C

112317919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: non coding transcript exon variant
orthologous variants: 55198684-A-G

112318012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: non coding transcript exon variant
orthologous variants: 55198777-G-T

112318029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: non coding transcript exon variant
orthologous variants: 55198794-G-T

http://identifiers.org/hco/10/GRCh38#112318083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55198848-C-A

112318083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55198848-C-T

112318090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55198857-T-C

112318167-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55198924-T-G

http://identifiers.org/hco/10/GRCh38#112318174-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55198929-A-C

112318346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55199070-T-C

112318430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55199142-A-G

112318584-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55199285-A-T

112318683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55199374-G-T

112320874-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55201428-T-A

112320874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55201428-T-C

112321637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55201990-G-A

112322025-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55202339-C-G

http://identifiers.org/hco/10/GRCh38#112322107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55202426-C-A

112322167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55202487-G-A

112322435-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55202673-G-C

112322488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55202712-T-C

112324490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: non coding transcript exon variant
orthologous variants: 55203589-C-T

http://identifiers.org/hco/10/GRCh38#112324511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55203610-C-A

112324511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: non coding transcript exon variant
orthologous variants: 55203610-C-T

http://identifiers.org/hco/10/GRCh38#112324614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55203696-C-A

112324618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55203700-G-T

112324690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55203760-G-A

112324713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55203783-T-C

112324723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55203793-G-A

112324723-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55203793-G-C

112324723-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55203793-G-T

http://identifiers.org/hco/10/GRCh38#112324760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55203828-C-A

112326925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55205240-G-A

http://identifiers.org/hco/10/GRCh38#112326984-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55205291-A-C

112326990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55205500-C-T

112327022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55205529-T-C

112327027-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55205534-C-G

112327027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55205534-C-T

112327039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55205546-T-C

112327039-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55205546-T-G

http://identifiers.org/hco/10/GRCh38#112327052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55205559-C-A

112327054-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55205561-A-T

112327373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55205881-A-G

112327378-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55205886-A-T

112330376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55207558-G-A

112330533-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55207693-G-C

112330607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55207801-A-G

112330607-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55207801-A-T

112330648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55207842-T-C

112331425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55208023-T-C

112331596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55208182-T-C

112331845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55208384-T-C

112331871-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55208391-T-A

112332227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55208746-C-T

112332278-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55208799-T-G

112332454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55208970-G-A

112332454-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55208970-G-C

112332461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55208977-C-T

112333669-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55209501-C-G

112333697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55209529-T-C

112333701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55209532-T-C

112333738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55209552-C-T

112333801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55209596-G-A

112333856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55209650-C-T

112334282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55210037-T-C

112334373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55210117-G-A

112334438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55210168-T-C

112334438-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55210168-T-G

http://identifiers.org/hco/10/GRCh38#112335147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55210866-C-A

112335200-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55210938-C-G

112335316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55211029-C-T

112335430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55211101-C-T

112335463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55211138-G-A

112335638-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55211315-T-G

112335996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55211655-C-T

112336019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55211678-G-A

112336119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55211763-A-G

112336146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55211788-G-T

112336222-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55211853-G-C

112336281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55211985-G-A

112336337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55212037-A-G

http://identifiers.org/hco/10/GRCh38#112336379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55212072-C-A

112336379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55212072-C-T

112336387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55212080-G-T

112336389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55212082-A-G

112336390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55212083-G-A

112336390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55212083-G-T

112336398-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55212091-G-C

112336398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55212091-G-T

112336570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55212474-G-A

112336570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55212474-G-T

112336935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55212828-C-T

112336937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55212830-T-C

112337048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55212914-G-T

112337049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55212915-G-A

112337131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55212960-A-G

112337267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55213102-A-G

112337341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55213174-T-C

112338809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55214116-T-C

112338882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55214214-T-C

112338942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55214298-T-C

112338942-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55214298-T-G

112338962-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55214318-C-G

112338962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55214318-C-T

http://identifiers.org/hco/10/GRCh38#112339010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55214368-C-A

112339010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55214368-C-T

112339061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: non coding transcript exon variant
orthologous variants: 55214405-T-C

http://identifiers.org/hco/10/GRCh38#112339125-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55214469-A-C

112339163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: non coding transcript exon variant
orthologous variants: 55214507-C-T

http://identifiers.org/hco/10/GRCh38#112339176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55214520-C-A

112339176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: non coding transcript exon variant
orthologous variants: 55214520-C-T

112339185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 55214529-G-T

112339495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55214795-G-A

112339495-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55214795-G-C

112339920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55215188-G-T

112339927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55215195-T-C

112339950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55215215-G-A

112340028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55215264-G-T

112340076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55215310-G-T

http://identifiers.org/hco/10/GRCh38#112340114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55215348-C-A

http://identifiers.org/hco/10/GRCh38#112340118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55215352-C-A

112340118-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55215352-C-G

112340118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55215352-C-T

http://identifiers.org/hco/10/GRCh38#112340162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55215390-C-A

112340826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: non coding transcript exon variant
orthologous variants: 55215844-C-T

http://identifiers.org/hco/10/GRCh38#112340859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55215892-C-A

112340873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: non coding transcript exon variant
orthologous variants: 55215906-G-T

112340884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: non coding transcript exon variant
orthologous variants: 55215917-G-T

112340903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 55215936-C-T

http://identifiers.org/hco/10/GRCh38#112340920-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55215964-C-A

112340960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55216005-T-C

112341207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55216235-T-C

http://identifiers.org/hco/10/GRCh38#112341535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55216483-C-A

112341535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55216483-C-T

112341606-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55216524-C-G

112341606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55216524-C-T

http://identifiers.org/hco/10/GRCh38#112341667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55216588-C-A

112341721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: non coding transcript exon variant
orthologous variants: 55216642-T-C

112341773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55216696-G-A

112341808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55216731-G-A

http://identifiers.org/hco/10/GRCh38#112341851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55216992-C-A

112341853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55217005-A-G

http://identifiers.org/hco/10/GRCh38#112341919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55217082-C-A

112341919-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55217082-C-G

112342020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55217190-A-G

112342025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55217195-C-T

112342073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55217235-C-T

112342872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55217738-G-A

112342938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55217810-G-T

http://identifiers.org/hco/10/GRCh38#112343174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55218208-C-A

112343174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55218208-C-T

http://identifiers.org/hco/10/GRCh38#112343185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55218219-C-A

112343234-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55218268-T-A

112343234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55218268-T-C

112343561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55218546-C-T

112343608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55218598-C-T

112343950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55218879-T-C

112343991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55218920-C-T

112344178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55219086-A-G

112345853-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55219314-G-C

112345853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55219314-G-T

http://identifiers.org/hco/10/GRCh38#112345862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55219323-C-A

112345862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55219323-C-T

http://identifiers.org/hco/10/GRCh38#112345863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55219324-C-A

112345863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55219324-C-T

112345866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55219327-A-G

112345869-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55219330-A-T

http://identifiers.org/hco/10/GRCh38#112345916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55219376-C-A

112345916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55219376-C-T

112345929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55219388-G-T

112345971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55219430-G-T

112346178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55219619-T-C

112346207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55219636-G-A

112346207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55219636-G-T

http://identifiers.org/hco/10/GRCh38#112346306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55219728-C-A

112346306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55219728-C-T

112347892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55220968-A-G

112348083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55221428-A-G

112348236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: non coding transcript exon variant
orthologous variants: 55221544-T-C

112348438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55221747-A-G

112348730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55222041-G-A

112348769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55222069-T-C

112349001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55222309-T-C

112349067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55222395-C-T

112349235-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55222544-T-A

112349279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55222587-A-G

112349488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55222699-C-T

http://identifiers.org/hco/10/GRCh38#112349581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55222791-C-A

112351616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55223868-G-A

112351616-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55223868-G-C

112351616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55223868-G-T

http://identifiers.org/hco/10/GRCh38#112351618-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55223870-A-C

112351618-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55223870-A-T

112351698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55223942-T-C

112351800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: non coding transcript exon variant
orthologous variants: 55224035-G-A

112351800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: non coding transcript exon variant
orthologous variants: 55224035-G-T

112351912-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55224163-T-A

112351973-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55224254-C-G

112351976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55224257-T-C

112352152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55224619-T-C

112352225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55224677-G-A

112352261-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55224701-G-T

112352271-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55224711-C-G

112353276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55225533-A-G

112353295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55225552-C-T

112353343-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55225600-T-G

112353583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55225825-A-G

http://identifiers.org/hco/10/GRCh38#112353809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55226147-C-A

112353834-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 55226174-C-G

112353846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: non coding transcript exon variant
orthologous variants: 55226186-G-A

112353846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: non coding transcript exon variant
orthologous variants: 55226186-G-T

112354002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: non coding transcript exon variant
orthologous variants: 55226342-G-A

112354254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55226610-C-T

112354299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55226642-G-T

112354328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55226674-G-A

112354961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55228344-A-G

112354971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55228353-G-A

112356109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55229164-T-C

http://identifiers.org/hco/10/GRCh38#112356150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55229212-C-A

http://identifiers.org/hco/10/GRCh38#112356312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#55229376-C-A

112356312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: non coding transcript exon variant
orthologous variants: 55229376-C-T

112356403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: non coding transcript exon variant
orthologous variants: 55229476-G-A

112356424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: non coding transcript exon variant
orthologous variants: 55229497-G-T

112356495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: non coding transcript exon variant
orthologous variants: 55229568-G-A

112356553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: non coding transcript exon variant
orthologous variants: 55229626-G-A

112356553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31863
most severe consequence: non coding transcript exon variant
orthologous variants: 55229626-G-T