http://identifiers.org/hco/2/GRCh38#186694138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#83643057-C-A

186694138-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 83643057-C-G

186694138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 83643057-C-T

186694367-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 83643277-A-T

186694464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron_variant, undefined
orthologous variants: 83643376-G-T

186694515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron_variant, undefined
orthologous variants: 83643432-T-C

186694515-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron_variant, undefined
orthologous variants: 83643432-T-G

186694527-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron_variant, undefined
orthologous variants: 83643439-T-G

186694531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron_variant, undefined
orthologous variants: 83643443-T-C

186694531-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron_variant, undefined
orthologous variants: 83643443-T-G

186694655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron_variant, undefined
orthologous variants: 83643535-C-T

186694823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron_variant, undefined
orthologous variants: 83643732-C-T

186695113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron_variant, undefined
orthologous variants: 83644023-T-C

http://identifiers.org/hco/2/GRCh38#186695308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#83644215-C-A

186695308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83644215-C-T

186695382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83644292-G-T

186695485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83644446-A-G

186695603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83644565-A-G

186695987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83644908-A-G

186696009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83644925-T-C

186696126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83645045-G-A

http://identifiers.org/hco/2/GRCh38#186696260-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#83645172-A-C

http://identifiers.org/hco/2/GRCh38#186696437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#83645322-C-A

186696437-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83645322-C-G

186696437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83645322-C-T

186697641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron_variant, undefined
orthologous variants: 83646237-C-T

http://identifiers.org/hco/2/GRCh38#186697914-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#83646469-A-C

186698262-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83646818-G-T

186698266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83646822-T-C

186698342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83646892-G-A

186698386-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83646967-T-G

186698393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83646977-T-C

186701699-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83648598-T-A

186701964-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83648842-C-G

186701981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83648859-G-T

186702500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83649249-T-C

186702649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83649388-G-T

186702731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83649466-A-G

186703253-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83649947-T-A

186703567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83650277-G-A

186703598-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83650403-C-G

186703676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83650485-G-A

186703813-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83650617-T-A

186703874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83650688-C-T

186704059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83650855-A-G

186704375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83651716-T-C

186704586-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83651863-A-T

186704767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83652031-C-T

186704808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83652073-T-C

186705444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83652550-G-A

186705694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83652777-G-A

http://identifiers.org/hco/2/GRCh38#186705757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#83652835-C-A

186705757-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83652835-C-G

186706320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83653351-A-G

http://identifiers.org/hco/2/GRCh38#186706461-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#83653490-A-C

186706461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83653490-A-G

186706653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83653658-T-C

186706657-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83653662-C-G

186706657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83653662-C-T

http://identifiers.org/hco/2/GRCh38#186707179-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#83654202-A-C

186709608-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83655054-G-C

186709643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83655086-A-G

186709675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83655118-A-G

186709734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83655179-G-A

186709734-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83655179-G-C

186710000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83655359-C-T

186710360-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83655827-A-T

186710394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83655866-G-A

186710765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83656241-A-G

186710869-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83656343-T-A

186710878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83656352-G-A

186710879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83656353-T-C

186711095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83656573-T-C

186711267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83656772-T-C

http://identifiers.org/hco/2/GRCh38#186711567-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#83657000-A-C

186711749-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83657168-T-G

186712396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83657535-G-A

186712402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83657541-C-T

186712414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83657553-G-T

186712627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83657754-C-T

186712884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83658002-C-T

186713196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83658481-A-G

186713238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83658535-G-A

186713674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83659103-G-A

186713721-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83659145-G-C

186713869-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83659327-G-C

186714021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83659494-G-A

186714305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83659809-T-C

186714373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83659875-A-G

186714654-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83660139-G-C

186714667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83660152-A-G

186714669-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83660154-T-G

186717812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83663570-T-C

186718195-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83663906-G-C

186718325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83664020-G-T

186718328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83664025-T-C

186718431-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83664146-A-T

186718455-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83665104-A-T

186718682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83665331-A-G

186718700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83665349-C-T

186718701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83665350-G-A

186718761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83665401-G-T

http://identifiers.org/hco/2/GRCh38#186718779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#83665419-C-A

186719368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83665947-A-G

186719477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83666055-C-T

http://identifiers.org/hco/2/GRCh38#186719567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#83666137-C-A

http://identifiers.org/hco/2/GRCh38#186719570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#83666140-C-A

186720942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83667059-C-T

186720960-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83667077-T-A

186721002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83667124-A-G

186721329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83667417-A-G

186721382-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83667469-T-G

http://identifiers.org/hco/2/GRCh38#186721411-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#83667493-A-C

186721411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83667493-A-G

186722205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83669886-C-T

186722579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83670230-C-T

186723156-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83670729-T-A

186723231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83670803-G-A

186723280-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83670854-T-G

186723281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83670855-A-G

186723290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83670864-T-C

http://identifiers.org/hco/2/GRCh38#186723338-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#83670914-C-A

186723341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83670917-A-G

186723709-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83673168-A-T

186724017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83673450-A-G

186725953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83673757-G-A

186725976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83673778-A-G

186726172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83673945-G-A

186726273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83674042-A-G

186726722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83674499-T-C

http://identifiers.org/hco/2/GRCh38#186726949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#83674684-C-A

186726949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83674684-C-T

186727451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83677143-G-A

186727684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83677420-G-A

186728006-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83677684-T-A

186728006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83677684-T-C

186728161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83677847-A-G

186728480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83678152-G-A

http://identifiers.org/hco/2/GRCh38#186728486-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#83678158-A-C

186728516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83678189-C-T

186728521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83678194-A-G

186728770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83678411-G-A

186729015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83678628-A-G

186729056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83678671-A-G

186729186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83678783-T-C

http://identifiers.org/hco/2/GRCh38#186729423-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#83679027-A-C

186729534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83679124-T-C

186729667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83679262-T-C

186730323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83679627-T-C

186730505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83679774-G-A

186730565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83679831-A-G

186730640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83679941-A-G

186730959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83680294-C-T

http://identifiers.org/hco/2/GRCh38#186730996-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#83680338-A-C

186731185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83680505-A-G

186731208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83680534-G-A

186731294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83680617-C-T

186736647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83681438-T-C

186736707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83681485-A-G

186736750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83681516-G-A

186736942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83681721-T-C

186737235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83681996-C-T

186737239-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83682000-G-C

186737265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83682050-C-T

186737266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83682051-G-A

186737302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83682092-G-A

186737345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83682131-T-C

http://identifiers.org/hco/2/GRCh38#186740098-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#83682481-A-C

186740098-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83682481-A-T

http://identifiers.org/hco/2/GRCh38#186740182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#83683659-C-A

http://identifiers.org/hco/2/GRCh38#186740197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#83683674-C-A

186740197-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83683674-C-G

186740265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: synonymous variant
orthologous variants: 83683751-C-T

186740289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: synonymous variant
orthologous variants: 83683775-A-G

186740468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 83683954-A-G

186740521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83683998-T-C

186740545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83684016-G-A

http://identifiers.org/hco/2/GRCh38#186740569-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#83684046-A-C

186740658-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83684134-C-G

186740733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83684205-C-T

186740794-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83684285-G-C

186743408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83685713-T-C

186743409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83685714-T-C

http://identifiers.org/hco/2/GRCh38#186743411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#83685716-C-A

186743411-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83685716-C-G

186743411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83685716-C-T

186743417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83685722-T-C

http://identifiers.org/hco/2/GRCh38#186743588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#83685886-C-A

http://identifiers.org/hco/2/GRCh38#186743718-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#83685990-A-C

186743833-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83686099-C-G

186743855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83686122-T-C

186744024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83686297-C-T

186744072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83686341-T-C

186744310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83686519-C-T

http://identifiers.org/hco/2/GRCh38#186745705-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#83686975-A-C

186745931-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83687283-G-C

186745931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83687283-G-T

http://identifiers.org/hco/2/GRCh38#186746009-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#83687358-A-C

186746364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83687700-T-C

http://identifiers.org/hco/2/GRCh38#186746517-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#83687833-A-C

http://identifiers.org/hco/2/GRCh38#186746536-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#83687852-A-C

186746536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83687852-A-G

186746697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83688001-G-A

186746697-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83688001-G-C

186747030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83688496-A-G

http://identifiers.org/hco/2/GRCh38#186747129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#83688599-C-A

186747129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: synonymous variant
orthologous variants: 83688599-C-T

186747225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: synonymous variant
orthologous variants: 83688695-A-G

186747225-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: synonymous variant
orthologous variants: 83688695-A-T

186747331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83688801-T-C

186748485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83689764-A-G

186748859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83690071-G-A

186748911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83690123-C-T

http://identifiers.org/hco/2/GRCh38#186748938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#83690148-C-A

186748938-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83690148-C-G

186751020-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83690639-T-A

http://identifiers.org/hco/2/GRCh38#186751427-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#83691041-A-C

186752864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83706022-A-G

186752919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83706077-T-C

186752948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83706106-A-G

186753798-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83706861-G-C

http://identifiers.org/hco/2/GRCh38#186753830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#83706897-C-A

186753830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83706897-C-T

186753894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83706967-G-A

186753900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83706974-A-G

186753900-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83706974-A-T

186754185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83707252-G-A

186754185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83707252-G-T

186754216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83707289-G-A

186754326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83707392-G-T

186761099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83708486-A-G

186761275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83708672-A-G

186761289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83708686-G-A

186761318-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83708715-G-C

186761318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: 83708715-G-T

http://identifiers.org/hco/2/GRCh38#186761387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#83709363-C-A

186762052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: synonymous variant
orthologous variants: 83710024-T-C

186762091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: synonymous variant
orthologous variants: 83710063-G-A

186762346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: synonymous variant
orthologous variants: 83710315-G-A

186762346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: synonymous variant
orthologous variants: 83710315-G-T

186762791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: stop gained
orthologous variants: 83710763-C-T

186762799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: synonymous variant
orthologous variants: 83710771-A-G

186762909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: 3 prime UTR variant
orthologous variants: 83710877-G-A

186763140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: 3 prime UTR variant
orthologous variants: 83711106-A-G

186763165-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: 3 prime UTR variant
orthologous variants: 83711128-A-T

186763166-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: 3 prime UTR variant
orthologous variants: 83711129-A-T

186763302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: 3 prime UTR variant
orthologous variants: 83711248-G-T

http://identifiers.org/hco/2/GRCh38#186763424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#83711360-C-A

186763791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: 3 prime UTR variant
orthologous variants: 83711678-A-G

186763906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: 3 prime UTR variant
orthologous variants: 83711809-G-A

186763906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: 3 prime UTR variant
orthologous variants: 83711809-G-T

186764055-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: 3 prime UTR variant
orthologous variants: 83711933-A-T

186764119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: 3 prime UTR variant
orthologous variants: 83711984-G-A

186764522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: 3 prime UTR variant
orthologous variants: 83712397-G-T

186764553-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: 3 prime UTR variant
orthologous variants: 83712427-T-A

http://identifiers.org/hco/2/GRCh38#186764650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#83712532-C-A

186764650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: 3 prime UTR variant
orthologous variants: 83712532-C-T

186764699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: 3 prime UTR variant
orthologous variants: 83712575-G-A

186764716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: 3 prime UTR variant
orthologous variants: 83712610-A-G

186764719-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: 3 prime UTR variant
orthologous variants: 83712613-T-A

186764719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: 3 prime UTR variant
orthologous variants: 83712613-T-C

186765564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: 3 prime UTR variant
orthologous variants: 83713438-A-G

186765662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29412
most severe consequence: 3 prime UTR variant
orthologous variants: 83713543-T-C