http://identifiers.org/hco/13/GRCh38#105459454-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#7571285-A-C

http://identifiers.org/hco/13/GRCh38#105459672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#7571494-C-A

105459717-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: non coding transcript exon variant
orthologous variants: 7571538-G-C

http://identifiers.org/hco/13/GRCh38#105459869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#7571690-C-A

105459886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: non coding transcript exon variant
orthologous variants: 7571707-G-A

105459914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: non coding transcript exon variant
orthologous variants: 7571733-G-A

105459956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: non coding transcript exon variant
orthologous variants: 7571775-G-A

105460058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: non coding transcript exon variant
orthologous variants: 7571875-C-T

105460523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: non coding transcript exon variant
orthologous variants: 7573111-C-T

105460527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: non coding transcript exon variant
orthologous variants: 7573115-A-G

http://identifiers.org/hco/13/GRCh38#105460553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#7573135-C-A

105460553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: non coding transcript exon variant
orthologous variants: 7573135-C-T

105460594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 7573178-A-G

105460596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 7573180-A-G

105460652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7573232-T-C

105460692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7573272-C-T

http://identifiers.org/hco/13/GRCh38#105460732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#7573311-C-A

105460732-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7573311-C-G

105460732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7573311-C-T

105460782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7573353-T-C

105460801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7573372-G-A

105460884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7573453-G-A

105460884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7573453-G-T

105460966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7573536-G-A

105461198-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7574295-T-A

105461198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7574295-T-C

105461198-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7574295-T-G

105461292-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7574392-A-T

105461350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7574440-A-G

105461365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7574449-A-G

105461549-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7574596-A-T

105461551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7574598-G-A

105461551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7574598-G-T

105461559-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7574606-G-C

http://identifiers.org/hco/13/GRCh38#105461564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#7574611-C-A

105461564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7574611-C-T

105461565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7574612-C-T

105461756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7574736-G-A

105461757-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7574737-T-A

105461797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7574778-G-T

105461822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7574797-G-T

105461835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7574810-G-T

http://identifiers.org/hco/13/GRCh38#105461924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#7574882-C-A

105462044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7575000-G-T

105462067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7575024-A-G

105462328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: non coding transcript exon variant
orthologous variants: 7575280-A-G

105462378-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: non coding transcript exon variant
orthologous variants: 7575330-C-G

105462378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: non coding transcript exon variant
orthologous variants: 7575330-C-T

105462383-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: non coding transcript exon variant
orthologous variants: 7575335-T-A

105462484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: non coding transcript exon variant
orthologous variants: 7575436-A-G

105462656-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7575599-T-A

105462755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7575702-C-T

http://identifiers.org/hco/13/GRCh38#105462881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#7575832-C-A

105462881-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7575832-C-G

105462881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7575832-C-T

105463085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7576020-A-G

105463242-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7576155-T-A

105463270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7576183-G-A

105463802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7576708-G-A

105463806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7576712-T-C

105463807-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7576713-C-G

105463846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7576752-C-T

105463967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7576867-T-C

105464265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7577357-A-G

105464265-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7577357-A-T

105464323-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7577401-T-A

105464343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7577421-G-A

105464343-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7577421-G-C

105464516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7577543-T-C

105464728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7577723-T-C

105464761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7577755-T-C

105465130-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7578102-T-A

105465130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7578102-T-C

105465175-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7578147-G-T

105465262-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7578230-G-T

http://identifiers.org/hco/13/GRCh38#105467127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#7581697-C-A

105467171-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7581737-T-A

105467183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7581750-G-T

http://identifiers.org/hco/13/GRCh38#105467224-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#7581780-A-C

105467224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7581780-A-G

105467282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7581828-T-C

105467337-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7581883-C-G

105467337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7581883-C-T

105468752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7582946-G-A

105468775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7582969-C-T

105468784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7582978-G-A

105468784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7582978-G-T

105468815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7583009-G-A

105468871-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7583064-C-G

105469181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7583382-C-T

105469228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7583425-T-C

105469475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7583699-C-T

105469588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7583810-C-T

105469698-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7583896-A-T

105469742-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7583943-C-G

105469751-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7583952-G-C

105469751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7583952-G-T

105469756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7583957-T-C

105469759-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7583960-T-A

105469760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7583961-A-G

http://identifiers.org/hco/13/GRCh38#105469791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#7583992-C-A

105469914-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7584097-T-G

105469946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7584128-G-A

105469956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7584138-A-G

105469992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7584181-T-C

105470109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7584299-C-T

105470110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7584300-A-G

105470110-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7584300-A-T

105470113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7584303-G-A

105470113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7584303-G-T

105470133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7584367-C-T

105470162-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7584391-A-T

105470250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7584478-G-T

105470255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7584483-G-A

105470265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7584491-C-T

105473296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7600271-C-T

105473389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7600343-G-T

105473469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7600423-T-C

105473500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7600458-G-A

105473583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7600556-T-C

105473694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7600663-G-A

105473869-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7600834-A-T

105473876-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7600841-T-G

105473924-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7600889-C-G

105473924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7600889-C-T

105474001-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7600965-T-A

105474001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7600965-T-C

105474193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7601258-G-A

105474334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7601389-C-T

105474463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7601500-C-T

105475078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 7603391-T-C

105475087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7603400-G-A

105475087-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7603400-G-C

105475155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7603467-G-T

http://identifiers.org/hco/13/GRCh38#105475178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#7603490-C-A

105475178-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7603490-C-G

http://identifiers.org/hco/13/GRCh38#105475264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#7603575-C-A

105475355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7603666-C-T

105475384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7603695-G-A

105475442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7603751-T-C

105475485-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7603794-T-A

105475485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7603794-T-C

105475568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7603877-A-G

105475861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7604160-A-G

105476053-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7604293-T-G

105476068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7604308-C-T

105476102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7604333-A-G

105476113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7604344-C-T

105476115-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7604346-T-G

105476163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7604396-A-G

105476174-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7604407-C-G

http://identifiers.org/hco/13/GRCh38#105476524-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#7604880-A-C

105476524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7604880-A-G

105476543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7604899-G-A

105476543-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7604899-G-C

105476831-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7605181-C-G

105476882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7605208-T-C

105476882-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7605208-T-G

105477002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7605325-A-G

105477055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7605374-T-C

105477150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7605448-G-T

105477275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7605551-G-A

105477275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7605551-G-T

105477295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7605570-G-A

105477318-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7605595-T-A

http://identifiers.org/hco/13/GRCh38#105487033-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#7608208-C-A

105487338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7608518-T-C

http://identifiers.org/hco/13/GRCh38#105487436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#7609425-C-A

105487453-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7609442-T-G

105487486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7609474-A-G

105487487-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7609475-G-C

105487556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7609542-G-A

105487755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7609624-C-T

105487764-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7609633-G-C

105487837-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7609714-T-G

105487886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7609749-C-T

http://identifiers.org/hco/13/GRCh38#105488170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#7610030-C-A

105488364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7610239-C-T

105488551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7610405-A-G

105488603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7610449-C-T

105488651-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7610485-C-G

105488659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7610492-C-T

105488749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7610576-G-T

105488839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7610657-T-C

105488961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7610778-A-G

105489209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7611147-T-C

105489251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7611196-G-A

http://identifiers.org/hco/13/GRCh38#105489452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#7611392-C-A

105489553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7611498-C-T

http://identifiers.org/hco/13/GRCh38#105489650-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#7611569-A-C

105489650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7611569-A-G

http://identifiers.org/hco/13/GRCh38#105490562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#7613179-C-A

105490968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7613539-T-C

http://identifiers.org/hco/13/GRCh38#105490970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#7613541-C-A

105490970-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7613541-C-G

105490970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7613541-C-T

105491114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: non coding transcript exon variant
orthologous variants: 7613740-A-G

105491315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7613934-G-A

105491402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7614018-G-A

105491543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7614174-G-T

105491575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7614199-A-G

105491596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7614220-T-C

105492134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: non coding transcript exon variant
orthologous variants: 7614598-A-G

105493568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7616921-C-T

105493576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7616929-G-A

105493776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7617136-G-A

105493960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7617278-A-G

105494239-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7617469-A-T

105494249-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7617479-T-A

http://identifiers.org/hco/13/GRCh38#105494250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#7617480-C-A

105494638-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7617898-T-G

105494665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7617925-A-G

105494938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7618197-C-T

105494980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7618233-A-G

http://identifiers.org/hco/13/GRCh38#105495027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#7618277-C-A

105495095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7618342-G-A

http://identifiers.org/hco/13/GRCh38#105495167-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#7618417-A-C

105495196-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7618447-C-G

105495532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7618623-C-T

105495554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7618652-T-C

105495572-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7618670-G-C

105495906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7619016-G-A

105495921-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7619031-G-C

105495996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7619094-C-T

105496026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7619124-G-A

105496041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7619140-A-G

105496132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7619233-G-A

105496132-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7619233-G-C

105496132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7619233-G-T

105496188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7619286-C-T

105496528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7619618-T-C

105496563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7619653-A-G

105496590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7619682-G-A

105496770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7619873-C-T

105496908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7619996-A-G

105496910-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7619998-T-A

http://identifiers.org/hco/13/GRCh38#105496972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#7620051-C-A

105497201-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7620280-T-G

105497264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7620343-T-C

105497360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7620437-A-G

105497421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7620499-A-G

http://identifiers.org/hco/13/GRCh38#105497434-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#7620512-A-C

105497434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7620512-A-G

105498824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7621532-C-T

105498932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7621614-G-A

http://identifiers.org/hco/13/GRCh38#105499048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#7621731-C-A

105499048-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7621731-C-G

105499128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7621811-C-T

105499129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7621812-G-A

105499256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7621939-T-C

105499624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7622306-G-A

105499624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7622306-G-T

105499652-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7622324-T-G

105499732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7622406-G-A

http://identifiers.org/hco/13/GRCh38#105499853-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#7622757-A-C

105499912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7622899-G-T

105499927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7622922-G-A

105499946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7622942-G-A

105500252-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7623213-T-A

105500364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7623318-T-C

105500435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7623388-C-T

105500626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7623568-T-C

http://identifiers.org/hco/13/GRCh38#105500916-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#7623771-A-C

105500916-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7623771-A-T

105501264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7624114-A-G

http://identifiers.org/hco/13/GRCh38#105501916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#7625374-C-A

105501923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7625383-A-G

105501962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7625420-C-T

105502373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7625833-T-C

105502417-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7625867-A-T

http://identifiers.org/hco/13/GRCh38#105502506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#7625956-C-A

105502506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7625956-C-T

105502533-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7625983-T-A

105502750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7626190-T-C

105503081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7626532-C-T

105503854-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7627195-C-G

105504659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7627952-G-A

105504659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7627952-G-T

105504922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7628197-T-C

http://identifiers.org/hco/13/GRCh38#105504927-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#7628202-A-C