6144164-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: 3 prime UTR variant
orthologous variants: 37051240-C-G

6144292-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: 3 prime UTR variant
orthologous variants: 37051341-A-T

http://identifiers.org/hco/6/GRCh38#6144307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37051355-C-A

6144342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: 3 prime UTR variant
orthologous variants: 37051398-G-A

6144342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: 3 prime UTR variant
orthologous variants: 37051398-G-T

6144412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: 3 prime UTR variant
orthologous variants: 37051523-G-T

6144580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: 3 prime UTR variant
orthologous variants: 37051690-T-C

6144695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: 3 prime UTR variant
orthologous variants: 37051800-C-T

6144697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: 3 prime UTR variant
orthologous variants: 37051802-G-A

6144735-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: 3 prime UTR variant
orthologous variants: 37051831-G-C

6144735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: 3 prime UTR variant
orthologous variants: 37051831-G-T

6144899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: 3 prime UTR variant
orthologous variants: 37052002-A-G

6144899-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: 3 prime UTR variant
orthologous variants: 37052002-A-T

6144991-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: 3 prime UTR variant
orthologous variants: 37052090-C-G

6144991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: 3 prime UTR variant
orthologous variants: 37052090-C-T

http://identifiers.org/hco/6/GRCh38#6145001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37052100-C-A

http://identifiers.org/hco/6/GRCh38#6145224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37052344-C-A

6145224-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: 3 prime UTR variant
orthologous variants: 37052344-C-G

6145224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: 3 prime UTR variant
orthologous variants: 37052344-C-T

http://identifiers.org/hco/6/GRCh38#6145280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37052395-C-A

6145317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: 3 prime UTR variant
orthologous variants: 37052435-G-A

6145367-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: 3 prime UTR variant
orthologous variants: 37052485-G-C

6145367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: 3 prime UTR variant
orthologous variants: 37052485-G-T

http://identifiers.org/hco/6/GRCh38#6145423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37052551-C-A

6145432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: 3 prime UTR variant
orthologous variants: 37052560-T-C

6145440-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: 3 prime UTR variant
orthologous variants: 37052568-T-A

http://identifiers.org/hco/6/GRCh38#6145444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37052572-C-A

6145444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: 3 prime UTR variant
orthologous variants: 37052572-C-T

http://identifiers.org/hco/6/GRCh38#6145459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37052585-C-A

6145459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: 3 prime UTR variant
orthologous variants: 37052585-C-T

6145479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: 3 prime UTR variant
orthologous variants: 37052605-G-T

http://identifiers.org/hco/6/GRCh38#6145484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37052610-C-A

6145484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: 3 prime UTR variant
orthologous variants: 37052610-C-T

http://identifiers.org/hco/6/GRCh38#6145577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37052697-C-A

6145577-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: 3 prime UTR variant
orthologous variants: 37052697-C-G

6145577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: 3 prime UTR variant
orthologous variants: 37052697-C-T

http://identifiers.org/hco/6/GRCh38#6145607-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37052727-C-A

6145607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: 3 prime UTR variant
orthologous variants: 37052727-C-T

6145646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: synonymous variant
orthologous variants: 37052766-C-T

6145694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: synonymous variant
orthologous variants: 37052814-G-A

6145751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: synonymous variant
orthologous variants: 37052871-G-A

6145751-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: synonymous variant
orthologous variants: 37052871-G-C

6145752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: missense variant
orthologous variants: 37052872-G-A

http://identifiers.org/hco/6/GRCh38#6145795-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37052914-A-C

6145827-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37052945-C-G

http://identifiers.org/hco/6/GRCh38#6145872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37052991-C-A

6145872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37052991-C-T

http://identifiers.org/hco/6/GRCh38#6145890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37053015-C-A

6145890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37053015-C-T

6147461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37057202-A-G

6147596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37057342-C-T

6147662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37057405-G-A

6147743-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37057489-C-G

6147745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37057491-T-C

6147793-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37057522-T-A

6147859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37057600-A-G

6148188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37057916-G-A

6148188-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37057916-G-C

6148235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37057972-C-T

6148263-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37058009-G-T

6148358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37058104-C-T

6148454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37058198-G-A

6148663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37058376-G-A

6148664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37058377-G-A

6148664-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37058377-G-C

6148818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37058514-C-T

6149410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37058576-C-T

6149412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37058578-C-T

6149649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37058815-G-A

6149686-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37058852-T-G

6149862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37059011-A-G

6150102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37059783-T-C

6150187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37059860-C-T

6150195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37059868-G-T

6150215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37059888-G-A

6150215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37059888-G-T

6150290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37059961-G-A

6150472-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37060143-A-T

http://identifiers.org/hco/6/GRCh38#6150697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37060348-C-A

6150813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37060463-A-G

6150852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37060497-A-G

6151055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37060667-A-G

6151686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37061384-G-A

6151686-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37061384-G-C

6151702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37061400-C-T

6151724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37061421-G-T

6151751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37061613-A-G

http://identifiers.org/hco/6/GRCh38#6151755-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37061617-A-C

6151755-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37061617-A-T

6151792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37061696-T-C

6151960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37061874-G-A

6151967-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37061881-G-C

http://identifiers.org/hco/6/GRCh38#6152000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37061914-C-A

6152072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37061981-G-T

6152079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37061988-G-T

6152110-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37062019-C-G

6152110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37062019-C-T

6152305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37062209-A-G

http://identifiers.org/hco/6/GRCh38#6152448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37062343-C-A

6152462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37062357-T-C

6152486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37062379-C-T

6152503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37062393-T-C

http://identifiers.org/hco/6/GRCh38#6152957-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37064566-A-C

6153544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37064976-C-T

6153723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37065159-T-C

http://identifiers.org/hco/6/GRCh38#6154142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37065537-C-A

6154142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37065537-C-T

6154175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37065554-G-A

6154249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37065597-G-A

6154249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37065597-G-T

6154352-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37065677-T-G

6154469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37065792-G-A

6154968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37066184-G-T

6155291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37067611-G-T

6155403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37067724-G-A

6155403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37067724-G-T

6155439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37067750-G-A

6155448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37067759-G-A

6156827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37069592-G-A

6157082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37069846-T-C

6157281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37070020-G-A

6157514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37070206-G-A

6157514-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37070206-G-C

6157556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37070248-A-G

6157758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37070441-A-G

6157896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37070716-C-T

http://identifiers.org/hco/6/GRCh38#6157903-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37070723-A-C

6158109-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37070905-C-G

6158109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37070905-C-T

6159243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37071747-A-G

6159283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37071789-C-T

6159331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37071815-G-A

6159414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37071899-T-C

6159480-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37071962-G-C

6159503-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37071986-G-C

6161675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37072614-G-A

6161753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37072692-T-C

6161797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37072735-G-A

6161809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37072747-A-G

6162024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37072978-C-T

6162595-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37073447-C-G

6162595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37073447-C-T

6162603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37073455-C-T

http://identifiers.org/hco/6/GRCh38#6162929-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37073735-A-C

6163043-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37073826-T-G

6163064-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37073845-G-C

6163064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37073845-G-T

6163065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37073887-G-A

6163158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37073980-C-T

6163169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37073991-T-C

6163174-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37073998-G-C

6163174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37073998-G-T

6163288-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37074123-G-C

6163288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37074123-G-T

6164832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37074259-C-T

6164849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37074279-C-T

6164867-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37074297-T-A

6164870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37074300-G-T

http://identifiers.org/hco/6/GRCh38#6164882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37074330-C-A

6164984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37074431-A-G

6165285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37074698-G-A

6165752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37075147-A-G

6165859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37075268-G-A

6166003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37075418-G-A

6166035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37075449-C-T

6166041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37075455-C-T

6166081-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37075491-G-C

6166090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37075499-C-T

6166246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37075658-A-G

http://identifiers.org/hco/6/GRCh38#6166262-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37075674-A-C

6166971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37076331-G-A

http://identifiers.org/hco/6/GRCh38#6167261-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37076611-A-C

6167277-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37076627-A-T

http://identifiers.org/hco/6/GRCh38#6167367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37076703-C-A

6167367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37076703-C-T

6167436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37076760-A-G

6167439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37076763-A-G

6167443-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37076767-G-C

6167485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: synonymous variant
orthologous variants: 37076807-C-T

http://identifiers.org/hco/6/GRCh38#6167648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37076970-C-A

6167648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37076970-C-T

6167659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37076985-G-A

6167659-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37076985-G-C

6167732-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37077053-C-G

6167732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37077053-C-T

http://identifiers.org/hco/6/GRCh38#6167735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37077056-C-A

6167735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37077056-C-T

6168430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37077514-T-C

6168431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37077515-C-T

http://identifiers.org/hco/6/GRCh38#6170157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37077573-C-A

6170157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37077573-C-T

6170167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37077583-G-A

6170239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37077652-T-C

6170449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37077879-T-C

6170658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37078086-T-C

6170820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37078242-G-A

6170863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37078285-T-C

6171001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37078435-G-A

6171001-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37078435-G-C

6171065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37078643-G-A

6171065-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37078643-G-C

http://identifiers.org/hco/6/GRCh38#6171335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37078852-C-A

6171483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37078962-G-A

6172892-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37080815-G-C

6172988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37080888-G-A

6173065-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37080979-C-G

6173075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37080989-G-A

6173290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37081208-C-T

6173776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37081591-A-G

6174469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37081863-G-A

6174469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37081863-G-T

http://identifiers.org/hco/6/GRCh38#6174518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37081897-C-A

6174518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37081897-C-T

6174596-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: synonymous variant
orthologous variants: 37081972-C-G

6174596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: synonymous variant
orthologous variants: 37081972-C-T

6174597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: missense variant
orthologous variants: 37081973-G-A

6174938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37082308-C-T

6175392-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37082727-C-G

http://identifiers.org/hco/6/GRCh38#6175563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37082864-C-A

6175570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37082871-A-G

6175728-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37082996-A-T

6175858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37083115-G-A

6176029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37083524-T-C

http://identifiers.org/hco/6/GRCh38#6176111-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37083607-A-C

6176327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37083840-C-T

6176556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37083957-T-C

6177049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37084364-G-A

6177084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37084398-C-T

6177279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37084574-C-T

6177616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37084888-G-A

6177673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37084943-T-C

6177725-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37084983-C-G

6177918-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37085193-G-C

6177977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37085250-G-A

6178067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37085330-A-G

6178067-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37085330-A-T

6178230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37085460-G-A

6178234-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37085464-T-G

6178334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37085567-T-C

6178380-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37085618-A-T

6178462-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37085695-T-G

6178520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37085757-G-A

6178828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37085989-G-A

6178831-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37085992-C-G

6178832-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37085993-A-T

6178940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37086068-T-C

6178983-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37086112-G-C

6178983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37086112-G-T

6178989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37086118-G-A

6179045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37086142-G-A

6179275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37086289-T-C

6179420-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37086430-C-G

6179577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37086593-C-T

6179578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37086594-G-A

6179578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37086594-G-T

6179731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37086748-T-C

6179841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37086852-T-C

6179860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37086871-G-A

6179940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37086942-C-T

6179945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37086947-G-A

6180042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37087038-G-A

6180097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37087121-A-G

6180132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37087152-T-C

6180354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37087564-C-T

6180424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37087631-C-T

6180466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37087671-C-T

6180467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37087672-G-A

6180882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37088085-C-T

6181437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37089218-A-G

6181494-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37089275-C-G

6181563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37089342-T-C

6181850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37089741-G-A

6181850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37089741-G-T

6181941-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37089832-T-G

http://identifiers.org/hco/6/GRCh38#6181961-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37089852-A-C

6182046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: synonymous variant
orthologous variants: 37089935-G-A

http://identifiers.org/hco/6/GRCh38#6182094-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37089983-A-C

6182094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: synonymous variant
orthologous variants: 37089983-A-G

6182478-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37092648-C-G

6182478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37092648-C-T

6182574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37092748-A-G

6182663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37092820-C-T

6182774-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37092907-A-T

6182816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37092946-T-C

http://identifiers.org/hco/6/GRCh38#6182817-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37092947-A-C

6182817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37092947-A-G

6182897-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37093030-A-T

6182936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37093068-T-C

6183001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37093132-G-A

http://identifiers.org/hco/6/GRCh38#6183100-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37093223-A-C

6183125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37093247-G-A

6183176-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37093295-T-A

http://identifiers.org/hco/6/GRCh38#6183210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37093311-C-A

6183532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37093637-T-C

6183567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37093661-T-C

6183584-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37093678-C-G

6183584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37093678-C-T

6183587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37093681-A-G

6183633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37093727-C-T

6183650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37093744-G-A

6183650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37093744-G-T

6183652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37093746-A-G

6183857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37094042-G-T

6183918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37094103-G-A

6183920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37094105-G-A

http://identifiers.org/hco/6/GRCh38#6183958-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37094143-A-C

6183964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37094149-C-T

6184065-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37094255-T-A

6184065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37094255-T-C

6184114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37094303-C-T

6184139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37094327-A-G

6184143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37094331-G-T

6184181-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37094365-A-T

6184265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37094448-C-T

6184305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37094492-G-T

6184319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37094507-C-T

6184525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37094779-C-T

http://identifiers.org/hco/6/GRCh38#6184586-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37094840-A-C

6184655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37094907-A-G

6184798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37095043-G-A

http://identifiers.org/hco/6/GRCh38#6191328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37095947-C-A

6191328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37095947-C-T

http://identifiers.org/hco/6/GRCh38#6191389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37096017-C-A

6191389-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37096017-C-G

6191423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37096052-T-C

6191484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37096113-A-G

6191500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37096129-T-C

6191744-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, undefined
orthologous variants: 37096344-C-G

6191930-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37096737-G-C

6191945-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37096798-C-G

6191976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37096829-G-A

6191976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37096829-G-T

6192059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37096909-G-A

6192081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37096918-A-G

6192142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37096968-A-G

6192149-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37096975-C-G

6192183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37097008-G-A

6192251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37097089-G-T

6192375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37097180-A-G

http://identifiers.org/hco/6/GRCh38#6192380-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37097185-A-C

6192380-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37097185-A-T

6192414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37097217-A-G

6192663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37097450-C-T

6192707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37097492-C-T

6192801-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37097716-T-G

6192802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37097717-G-A

6193228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37098372-T-C

6193328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37098464-G-A

6193360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37098495-G-A

6193389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37098536-C-T

6193398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37098558-G-A

6193454-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37098625-T-G

http://identifiers.org/hco/6/GRCh38#6193818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37098982-C-A

6193818-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37098982-C-G

6193818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37098982-C-T

6193949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37099123-C-T

6193952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37099126-G-T

6194690-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37099792-T-G

6194700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37099802-C-T

6194712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37099815-A-G

6194778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37099882-T-C

6194780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37099884-A-G

6194998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37100116-G-T

6195049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37100165-C-T

http://identifiers.org/hco/6/GRCh38#6195105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37100223-C-A

http://identifiers.org/hco/6/GRCh38#6195115-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37100232-A-C

6195473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37100511-A-G

6195473-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37100511-A-T

6195613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37100660-T-C

http://identifiers.org/hco/6/GRCh38#6195743-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37100783-A-C

6195743-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37100783-A-T

6195899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37100945-A-G

6195953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37100998-C-T

6195957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37101002-G-T

6195964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37101009-G-T

6196094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37101167-G-A

6196378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37101704-T-C

6196489-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37101804-C-G

6196489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37101804-C-T

6196538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37101852-T-C

http://identifiers.org/hco/6/GRCh38#6196799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37102102-C-A

6196899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37102207-G-A

6197037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37102350-G-T

6197096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37102409-G-A

6197096-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37102409-G-T

http://identifiers.org/hco/6/GRCh38#6197101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37102414-C-A

6197101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37102414-C-T

6197148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37102461-A-G

6197302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: synonymous variant
orthologous variants: 37102585-T-C

6197308-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: missense variant
orthologous variants: 37102591-A-T

http://identifiers.org/hco/6/GRCh38#6197750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37102721-C-A

6197813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37102781-T-C

6197962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37102956-A-G

http://identifiers.org/hco/6/GRCh38#6198164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37103148-C-A

6198469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37103449-C-T

6198504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37103482-A-G

6198719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37103713-G-T

6198823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37103818-A-G

6198933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37103949-T-C

6199567-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37104195-T-A

6199647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37104249-G-T

6199791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37104385-C-T

6200588-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37105641-G-C

6200857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37105916-G-A

6200857-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37105916-G-C

6200982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37106005-A-G

http://identifiers.org/hco/6/GRCh38#6201097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37106090-C-A

6201187-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37106177-T-G

6201245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37106235-C-T

6201372-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37106355-C-G

http://identifiers.org/hco/6/GRCh38#6201382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37106365-C-A

6201382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37106365-C-T

6201436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37106403-C-T

6201640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37106563-G-A

6203662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37113806-C-T

6203716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37113858-T-C

6203803-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37113935-G-C

6203934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37114132-C-T

6203941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37114146-C-T

6203964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37114174-G-A

6204199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37114508-C-T

6204491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37114823-A-G

6204605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37114923-T-C

6204702-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37115022-G-C

6204755-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37115079-C-G

6204772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37115089-C-T

6204857-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37115163-C-G

6204857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37115163-C-T

6204864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37115170-G-A

6204992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37115304-G-A

6205224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37115685-C-T

http://identifiers.org/hco/6/GRCh38#6205235-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37115696-A-C

6205402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37115821-C-T

6205732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37116052-A-G

6205795-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37116125-T-A

6205876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37116207-G-A

6205891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37116218-T-C

6206139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37116452-T-C

6206283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37117479-G-A

6206393-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37117590-T-A

6206421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37117615-G-A

6206534-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37117706-G-T

http://identifiers.org/hco/6/GRCh38#6206662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37117816-C-A

6211068-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37122423-T-G

6211199-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37122570-C-G

6211199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37122570-C-T

6211239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37122607-A-G

6211344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37122717-A-G

6211382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37122755-A-G

6211389-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37122762-T-A

6211389-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37122762-T-G

6211527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37122900-A-G

http://identifiers.org/hco/6/GRCh38#6218347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37124394-C-A

6218357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37124405-A-G

6218908-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37124631-G-C

6218923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37124646-C-T

6219205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37124840-T-C

6219250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37124862-C-T

6219293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37124904-C-T

6219363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37124951-C-T

6219526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37125377-T-C

6219553-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37125404-C-G

6219926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37125898-G-A

6219926-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37125898-G-C

6220028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37126000-G-T

6220178-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37126126-C-G

6220430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37126324-G-A

6220547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37126433-G-A

6220563-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37126449-C-G

http://identifiers.org/hco/6/GRCh38#6221179-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37127067-A-C

6221194-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37127081-A-T

6221210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37127097-T-C

6221245-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37127129-G-C

6221516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37127390-G-A

6221523-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37127397-C-G

6221523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37127397-C-T

6221697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37127531-C-T

6221731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37127559-T-C

http://identifiers.org/hco/6/GRCh38#6221913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37127744-C-A

http://identifiers.org/hco/6/GRCh38#6221934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37127760-C-A

6221934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37127760-C-T

6221966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37127794-T-C

6222149-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: synonymous variant
orthologous variants: 37127981-T-A

6222149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: synonymous variant
orthologous variants: 37127981-T-C

6222149-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: synonymous variant
orthologous variants: 37127981-T-G

http://identifiers.org/hco/6/GRCh38#6222237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37128062-C-A

6222237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37128062-C-T

6222250-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37128077-G-C

http://identifiers.org/hco/6/GRCh38#6222267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37128093-C-A

6222281-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37128107-C-G

6222281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37128107-C-T

6222465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37128281-C-T

http://identifiers.org/hco/6/GRCh38#6222647-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37128438-A-C

6223039-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37128811-G-T

6223214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37128978-G-A

6223239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37129008-C-T

6223377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37129141-G-A

6223766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37129498-T-C

6224042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37129797-G-A

6224042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37129797-G-T

6224406-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37130138-A-T

http://identifiers.org/hco/6/GRCh38#6224551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37130284-C-A

6224551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37130284-C-T

6224598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37130330-G-A

6224598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37130330-G-T

6224653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37130385-T-C

6224866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 37130597-T-C

6224866-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 37130597-T-G

6224900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37130630-T-C

6224920-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37130637-G-C

6224920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37130637-G-T

6224956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37130673-C-T

6224983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37130702-T-C

6224989-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37130708-T-G

6225102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37130797-G-A

http://identifiers.org/hco/6/GRCh38#6225757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37131300-C-A

http://identifiers.org/hco/6/GRCh38#6225758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37131301-C-A

6225850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37131439-A-G

6226129-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37131768-G-C

6226252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37131879-A-G

6226678-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37132202-C-G

6226713-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37132241-A-T

6227004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37132476-A-G

6227004-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37132476-A-T

6227352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37133101-T-C

6227495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37133189-T-C

6227512-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37133206-C-G

6227518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37133212-C-T

6227796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37133454-G-A

6227796-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37133454-G-C

http://identifiers.org/hco/6/GRCh38#6228208-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37133871-A-C

6229027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37134494-A-G

6229224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37134605-A-G

6229325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37134698-G-A

6229436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37134807-C-T

6229505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37134868-C-T

6229540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37134893-G-A

6236488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37137438-T-C

6236830-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37137767-T-A

6237423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37138348-C-T

6237495-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37138421-C-G

http://identifiers.org/hco/6/GRCh38#6237677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37138609-C-A

6239080-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37142004-G-C

6239114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37142038-T-C

6239221-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37142129-C-G

6239492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37142369-T-C

6239543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37142439-T-C

6239549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37142445-T-C

6239551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37142447-T-C

6239786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37142702-G-A

6240173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37143260-G-T

6240320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37143407-G-A

6240517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37143576-G-A

6240558-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37143613-C-G

6241126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37144134-A-G

6241196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37144202-A-G

6241478-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37144465-T-A

6241478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37144465-T-C

6241548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37144530-G-A

6241588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37144567-C-T

6241903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37144863-G-T

6241926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37144887-A-G

http://identifiers.org/hco/6/GRCh38#6241934-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37144895-A-C

6241934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37144895-A-G

http://identifiers.org/hco/6/GRCh38#6241962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37144955-C-A

6242047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37145042-T-C

6242047-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37145042-T-G

6242252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37145205-T-C

6242409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37145366-C-T

http://identifiers.org/hco/6/GRCh38#6242535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37145490-C-A

6242909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37145895-A-G

6242909-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37145895-A-T

http://identifiers.org/hco/6/GRCh38#6243102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37146098-C-A

6243102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37146098-C-T

6243288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37146459-C-T

http://identifiers.org/hco/6/GRCh38#6243373-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37146602-A-C

6243723-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37146956-T-A

6243723-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37146956-T-G

http://identifiers.org/hco/6/GRCh38#6244291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37147513-C-A

6244291-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37147513-C-G

6244535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37147744-A-G

6244614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37147820-C-T

http://identifiers.org/hco/6/GRCh38#6244818-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37148380-A-C

http://identifiers.org/hco/6/GRCh38#6244840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37148401-C-A

6244840-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37148401-C-G

6244840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37148401-C-T

6245142-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37148667-A-T

6245202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37148711-T-C

6245576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37148797-G-A

6245658-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37148874-C-G

6245782-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37148996-C-G

6245807-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37149021-C-G

6245836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37149048-G-A

http://identifiers.org/hco/6/GRCh38#6245862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37149082-C-A

6245862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37149082-C-T

6246106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37149397-C-T

6246235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37149527-C-T

http://identifiers.org/hco/6/GRCh38#6246423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37149708-C-A

6246487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37149781-C-T

6246628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37149939-G-A

6246703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37149985-C-T

6247163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37150563-A-G

6247237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37150637-T-C

6247274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37150674-G-A

6247316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37150715-T-C

6247362-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37150763-G-C

6247433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37150828-T-C

6247465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37150859-C-T

6247470-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37150864-T-A

6247470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37150864-T-C

6247664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37150981-G-T

6247669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37150986-G-A

6247669-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37150986-G-C

6247689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37151006-A-G

6247750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37151068-C-T

6248431-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37152111-A-T

6248467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37152148-G-A

6248467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37152148-G-T

6248535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37152205-A-G

6248573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37152243-G-A

6249471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37153543-C-T

6250259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37154704-G-A

6250566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37155677-A-G

http://identifiers.org/hco/6/GRCh38#6250582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37155691-C-A

6250598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37155708-T-C

6250786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron variant
orthologous variants: 37155897-C-T

6250925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 37156036-A-G

6250947-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37156058-C-G

6251017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37156118-A-G

http://identifiers.org/hco/6/GRCh38#6251028-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37156130-A-C

6251028-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37156130-A-T

6251040-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37156139-T-A

6251449-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37156527-A-T

6251477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37156555-G-T

6254176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37161717-G-A

6254636-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37163053-G-C

6254857-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37163258-T-A

6255303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37164251-G-T

6255926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37164876-C-T

6256151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37165093-G-A

6256151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37165093-G-T

6256380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37165300-C-T

http://identifiers.org/hco/6/GRCh38#6256521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37165437-C-A

6256628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37165548-G-A

6256920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37165855-A-G

6257130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37166062-A-G

6257136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37166067-A-G

6257428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37166240-G-T

6258283-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37167165-A-T

6258383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37167481-G-A

6258516-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37167608-T-A

6258516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37167608-T-C

6258698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37167735-G-A

6259025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37168839-C-T

6259555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37169346-C-T

6259630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37169419-G-A

6259630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37169419-G-T

6259928-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37169736-C-G

6260073-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37169878-G-C

6260073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37169878-G-T

6264180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37170645-A-G

6264298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37170734-A-G

6264305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37170740-G-T

6264466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37170876-T-C

6265152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37171493-G-T

6265273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37171615-C-T

6265615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37171911-G-A

6265755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37172058-C-T

6266172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37172372-T-C

6266545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37172795-G-A

6266583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 37172833-G-A

6266646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 37172896-A-G

6266697-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 37172947-C-G

6266934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37174766-C-T

6266974-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37174806-G-C

6267022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37174856-T-C

6267034-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37174868-A-T

6267322-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37175092-G-C

6267434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37175224-G-A

6267533-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37175357-T-G

6270718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37176210-A-G

6270737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37176225-G-A

6270896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37176342-G-A

6271026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37176440-C-T

6271041-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37176454-G-C

6271081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37176493-G-A

6271278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37176748-T-C

6271377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37176847-C-T

6271402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37176872-T-C

http://identifiers.org/hco/6/GRCh38#6271455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37176914-C-A

6271525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37176982-C-T

6271543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37177000-C-T

6271546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37177003-T-C

6271646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37177107-A-G

6271746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37177200-G-A

6273244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37177696-T-C

6273255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37177707-C-T

6273312-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37177763-G-C

6273493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37177933-C-T

6273927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37178351-C-T

6275941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37183057-T-C

6276033-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37183128-G-C

6276033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37183128-G-T

6276072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37183167-C-T

6276189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37183260-G-A

6276446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37183493-G-A

6276739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37183769-G-T

6276814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37183841-T-C

6278114-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37184005-T-A

6278969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37184582-C-T

6279024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37184637-T-C

6279270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37184861-T-C

6279409-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37184989-T-G

6279484-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37185063-G-C

6279758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37185303-T-C

6280807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37187920-T-C

6280809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37187922-C-T

6280811-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37187924-T-A

6280811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37187924-T-C

6280845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37187956-C-T

6281309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37188149-A-G

6282289-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37189114-T-G

6282355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37189180-G-A

6282391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37189213-G-T

6282537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37189343-A-G

6282674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37189475-T-C

6282674-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37189475-T-G

6282802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37189582-T-C

6283382-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37190854-T-G

6283434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37190906-A-G

6283472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37190965-C-T

6283517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37191008-T-C

6283523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37191011-C-T

6283591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37191077-C-T

6283815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37191298-T-C

6284108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37191578-C-T

6284569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37195532-T-C

6284851-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37195789-C-G

6285454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37196935-A-G

6286688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37197238-T-C

6286898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37197408-T-C

6286903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37197413-G-A

6287170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37197680-A-G

6287224-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37197734-T-G

6287453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37197947-A-G

http://identifiers.org/hco/6/GRCh38#6289692-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37199578-A-C

6289932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37199786-C-T

6290289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37200265-G-A

6290527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37200521-C-T

6290528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37200522-G-A

6291883-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37203329-A-T

http://identifiers.org/hco/6/GRCh38#6292166-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37203493-A-C

6292169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37203496-G-A

http://identifiers.org/hco/6/GRCh38#6292245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37203576-C-A

6292394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37203667-G-A

6292714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37203994-G-A

6293144-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37204842-G-C

http://identifiers.org/hco/6/GRCh38#6293670-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37206290-A-C

6293683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37206348-C-T

6293819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37206553-G-A

6293826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37206560-A-G

http://identifiers.org/hco/6/GRCh38#6293834-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37206568-A-C

6293834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37206568-A-G

6293848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37206604-A-G

http://identifiers.org/hco/6/GRCh38#6293863-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37206621-A-C

6301393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37207505-T-C

6301722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37207787-G-T

6301846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37207921-C-T

http://identifiers.org/hco/6/GRCh38#6303751-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37208501-A-C

6303751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37208501-A-G

6303931-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37208673-G-C

6303931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37208673-G-T

6304006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37208746-T-C

6304892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37209249-G-A

6304892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37209249-G-T

6304945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37209304-T-C

6304980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37209336-G-A

6305006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37209364-T-C

http://identifiers.org/hco/6/GRCh38#6305059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37209404-C-A

http://identifiers.org/hco/6/GRCh38#6305069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37209413-C-A

http://identifiers.org/hco/6/GRCh38#6305074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37209418-C-A

6305074-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37209418-C-G

http://identifiers.org/hco/6/GRCh38#6305118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37209464-C-A

6305121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37209467-G-A

6305121-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37209467-G-C

6305121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37209467-G-T

6305257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37209557-A-G

6305257-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37209557-A-T

6305258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37209558-T-C

6305259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37209559-G-A

6305259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37209559-G-T

6305295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37209595-C-T

6305376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 37209670-A-G

6305376-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37209670-A-T

http://identifiers.org/hco/6/GRCh38#6305687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37209949-C-A

6305687-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37209949-C-G

6305694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37209954-G-A

6305694-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37209954-G-C

6305694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37209954-G-T

6306152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37210372-G-A

6306159-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37210379-A-T

6306316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37210538-C-T

6306353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37210573-G-T

6306594-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37210790-A-T

6306725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37210887-C-T

6306785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37210915-T-C

http://identifiers.org/hco/6/GRCh38#6306887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37211014-C-A

6306887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37211014-C-T

6306937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37211094-C-T

http://identifiers.org/hco/6/GRCh38#6307028-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37211184-C-A

6307232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37211387-C-T

6307250-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37211405-G-C

6307368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37211518-G-A

6307561-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37211962-T-A

6307561-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37211962-T-G

6307573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37211974-A-G

6307622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37212020-A-G

6307650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37212049-A-G

6308940-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37213758-C-G

6308988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37213806-C-T

6309012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37213833-G-A

6309068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37213892-C-T

6309096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37213920-A-G

6309615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37214652-G-A

6309706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37214744-G-T

6309856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37215157-A-G

6309864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37215165-T-C

http://identifiers.org/hco/6/GRCh38#6309912-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37215209-A-C

6309933-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37215243-G-C

6310372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37215606-C-T

6310513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37215932-T-C

6310518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37215937-G-A

6310518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37215937-G-T

6310632-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37216043-T-A

6310926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37216298-C-T

6311158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37216513-G-T

6311407-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37216766-G-T

6311585-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37216913-T-A

6311589-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37216917-T-G

6311668-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37216991-T-A

6311668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37216991-T-C

6311668-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37216991-T-G

http://identifiers.org/hco/6/GRCh38#6311779-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37217107-A-C

6311779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37217107-A-G

6311779-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37217107-A-T

6311895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37217222-T-C

6313108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37218682-T-C

6313197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37218776-G-A

6313197-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37218776-G-C

6313267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37218847-A-G

6313292-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37218872-T-G

6313314-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37218898-A-T

6313651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37219234-C-T

6313667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37219250-G-A

6313880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37219444-G-A

6313912-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37219478-G-C

http://identifiers.org/hco/6/GRCh38#6314000-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37219547-A-C

6314000-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37219547-A-T

6314020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37219582-C-T

6314021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37219583-G-A

6314021-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37219583-G-C

6314021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37219583-G-T

6314033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37219599-G-A

6314083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37219681-G-T

6314176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37219849-T-C

6314379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37220122-C-T

http://identifiers.org/hco/6/GRCh38#6314770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37220594-C-A

6314934-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 37227877-C-G

6315046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37227997-G-T

6315120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37228074-G-A

6315303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37228252-C-T

6315304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37228253-G-A

6315446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37228656-T-C

6315446-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37228656-T-G

6315495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37228704-A-G

6315805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37229141-T-C

http://identifiers.org/hco/6/GRCh38#6315897-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37229216-A-C

6316150-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37229397-T-A

6316150-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37229397-T-G

6316159-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37229406-T-A

6316159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37229406-T-C

6316172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37229419-C-T

6316202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37229449-C-T

6316203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37229450-G-A

6316793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37229979-A-G

6316980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37230140-C-T

6317212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37230350-G-A

6317808-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37230649-T-G

6317864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37230707-T-C

6317911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37230754-G-T

6317947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37230790-G-A

6318222-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37231039-C-G

6318378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37231188-G-A

6318481-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37231296-A-T

http://identifiers.org/hco/6/GRCh38#6318486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37231301-C-A

6318486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37231301-C-T

6318717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37231509-A-G

6318777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37231570-T-C

6318777-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37231570-T-G

6318778-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37231571-G-C

6318778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37231571-G-T

6318917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37231711-A-G

6319092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37231841-C-T

6319121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37231870-C-T

6319135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37231884-T-C

6319144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37231893-G-A

6319205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37231954-G-A

http://identifiers.org/hco/6/GRCh38#6319885-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37232531-A-C

6319898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37232544-G-A

6319898-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37232544-G-C

6320039-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37232689-G-T

6320050-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37232704-G-C

6320179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37232828-G-A

6320479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 37233024-G-T

http://identifiers.org/hco/6/GRCh38#6320894-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#37233422-A-C

6320963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3531
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37233496-G-T