http://identifiers.org/hco/7/GRCh38#89002359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#7111928-C-A

89002359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7111928-C-T

89002377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7111910-T-C

89002400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7111889-T-C

89002557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7111771-T-C

89002592-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7111744-A-T

http://identifiers.org/hco/7/GRCh38#89002792-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#7111593-A-C

89002895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7111513-G-A

89002924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7111484-A-G

http://identifiers.org/hco/7/GRCh38#89002958-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#7111450-A-C

89003107-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7111318-T-A

89003175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7111270-C-T

89003250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7111215-G-A

89003257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7111208-G-A

89003452-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7111019-C-G

89003506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7110967-A-G

89003535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7110938-T-C

89003538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7110935-A-G

89003696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7110790-G-A

89003696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7110790-G-T

89003761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7110723-A-G

http://identifiers.org/hco/7/GRCh38#89003773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#7110710-C-A

89003809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7110683-A-G

89003838-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7110654-C-G

89003838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7110654-C-T

89003844-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7110648-C-G

89003914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7110589-T-C

89003979-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7110546-T-A

89004014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7110512-G-A

89004074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7110466-G-A

89004134-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7110402-C-G

http://identifiers.org/hco/7/GRCh38#89004212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#7110325-C-A

89004280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7110257-T-C

89004348-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7110193-A-T

89004393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7110140-G-A

89004400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7110133-G-A

89004418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7110115-C-T

89004494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7110053-T-C

89004570-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7109977-G-C

89004733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7109824-A-G

89004879-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7109678-C-G

89004880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7109677-T-C

89010533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7108816-A-G

89010651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7108711-G-A

89010700-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7108664-A-T

89013261-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7108334-T-G

http://identifiers.org/hco/7/GRCh38#89013319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#7108282-C-A

89013328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7108273-A-G

89013383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7108220-A-G

89022490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7108057-C-T

89022558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7107994-C-T

89022611-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7107939-C-G

89022749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7107686-A-G

http://identifiers.org/hco/7/GRCh38#89023266-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#7106921-C-A

89023397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron_variant, undefined
orthologous variants: 7106790-A-G

89023445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron_variant, undefined
orthologous variants: 7106745-G-T

89023624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7106574-C-T

http://identifiers.org/hco/7/GRCh38#89023835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#7106394-C-A

89023846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7106383-C-T

89023881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7106348-C-T

89023925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7106303-A-G

http://identifiers.org/hco/7/GRCh38#89024081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#7106146-C-A

89024257-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7105961-C-G

89024398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7105839-A-G

89024399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7105838-T-C

89024519-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7105717-T-A

89024571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7105668-A-G

89024852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7104184-G-T

89024861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7104175-T-C

89024881-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7104155-C-G

89025174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7102492-A-G

89025238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7102427-T-C

http://identifiers.org/hco/7/GRCh38#89025276-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#7102389-A-C

89025294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7102373-T-C

89025346-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7102327-C-G

89025511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7101488-G-A

89025523-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7101476-T-G

89025568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7101451-C-T

89026536-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7100579-C-G

89026948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7099446-A-G

89027067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7099332-G-A

89027181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7099223-A-G

89027542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7098916-A-G

89027623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7098754-C-T

http://identifiers.org/hco/7/GRCh38#89027638-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#7098739-A-C

89027660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7098716-G-A

89027713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7098668-A-G

89027738-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7098637-T-G

89027746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7098629-G-A

89027832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron_variant, undefined
orthologous variants: 7098539-A-G

89027832-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron_variant, undefined
orthologous variants: 7098539-A-T

89028043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron_variant, undefined
orthologous variants: 7098348-T-C

89029681-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7098152-T-G

http://identifiers.org/hco/7/GRCh38#89029797-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#7098026-A-C

89030000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron_variant, undefined
orthologous variants: 7097847-G-T

89030001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron_variant, undefined
orthologous variants: 7097846-T-C

89030042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron_variant, undefined
orthologous variants: 7097805-A-G

http://identifiers.org/hco/7/GRCh38#89030044-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#7097803-A-C

89030239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7096731-T-C

89030530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7096457-C-T

89030535-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7096452-G-C

89030591-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7096403-C-G

89031343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7095949-A-G

89031429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7095859-A-G

89031516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7095778-A-G

http://identifiers.org/hco/7/GRCh38#89031609-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#7095699-A-C

89031652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7095656-C-T

89032021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7095368-G-T

89032116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7095267-A-G

89032117-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7095266-A-T

89032165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7095218-A-G

http://identifiers.org/hco/7/GRCh38#89032226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#7095151-C-A

89032233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7095144-G-A

89032233-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7095144-G-T

http://identifiers.org/hco/7/GRCh38#89032308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#7095100-C-A

89032308-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7095100-C-G

89032335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7095068-G-A

89032338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7095065-A-G

89032498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7091697-C-T

89032533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7091660-G-T

89032540-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7091653-T-A

89032560-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7091631-T-G

89032744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7091481-A-G

89032752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7091472-G-A

89032847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7091399-T-C

http://identifiers.org/hco/7/GRCh38#89032991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#7091275-C-A

89032991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7091275-C-T

89033248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7091050-A-G

89033380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7090950-G-A

89033485-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7090805-G-C

89034375-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7089572-T-A

89034466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7089473-G-A

89034867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7088994-A-G

89035607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7088229-G-A

89035782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7088060-T-C

89043160-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7086104-A-T

89043248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7086015-T-C

http://identifiers.org/hco/7/GRCh38#89043348-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#7085916-A-C

http://identifiers.org/hco/7/GRCh38#89043669-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#7085598-A-C

89046746-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7082673-T-A

89046746-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7082673-T-G

89046794-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7082624-T-A

89046914-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7082505-T-A

http://identifiers.org/hco/7/GRCh38#89047024-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#7082370-A-C

89048736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7081239-A-G

89049196-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7080787-C-G

89049319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7080712-C-T

89052053-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7072051-T-A

89052410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7071897-C-T

89052590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7071702-C-T

89052707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7071595-T-C

89052771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7071529-T-C

89053109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7070920-A-G

89053177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7070852-G-A

89053218-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7070811-T-G

89053247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7070782-C-T

89053309-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7070732-T-G

89053703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7070011-T-C

89053703-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7070011-T-G

89054286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7069445-T-C

89056440-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7068601-G-C

89056440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7068601-G-T

http://identifiers.org/hco/7/GRCh38#89056584-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#7068444-A-C

89056588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7068440-A-G

89077949-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7059038-T-G

89078095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7058887-C-T

89078231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7058669-T-C

89085066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7058181-G-A

89085066-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7058181-G-C

89085122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7058125-G-A

http://identifiers.org/hco/7/GRCh38#89085366-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#7057883-A-C

89085456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7057783-T-C

89085482-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7057757-C-G

89085545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7057698-G-A

89085637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7057611-G-A

89085647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7057601-G-A

89085782-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7057466-T-A

http://identifiers.org/hco/7/GRCh38#89085805-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#7057443-A-C

89085895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7057355-T-C

89086015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7057235-C-T

89086021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7057229-G-A

89086104-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7057148-T-G

89086518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7056639-T-C

89086577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7056584-A-G

89086633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7056529-C-T

89087171-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7056152-A-T

89087231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7056093-A-G

89087231-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7056093-A-T

89090606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7053409-G-A

89090759-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7053245-T-A

89090834-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7053176-A-T

89090882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7053129-A-G

89091021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7052987-G-A

89091066-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7052939-T-G

http://identifiers.org/hco/7/GRCh38#89091246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#7052742-C-A

89091274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7052714-A-G

89091325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7052667-T-C

89091361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7052632-A-G

http://identifiers.org/hco/7/GRCh38#89091605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#7052401-C-A

89096326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7044914-A-G

89096406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7044852-G-A

89096497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7044770-A-G

89096533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7044741-G-T

89096625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7044650-G-A

89096799-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7044488-G-C

89097020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7044319-T-C

89097033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7044306-C-T

89097326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7043998-T-C

89097329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7043995-T-C

http://identifiers.org/hco/7/GRCh38#89097364-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#7043960-A-C

89097371-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7043953-T-G

89097394-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7043932-T-A

89097401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7043925-C-T

89097422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7043904-A-G

89097528-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7043772-G-C

http://identifiers.org/hco/7/GRCh38#89097532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#7043768-C-A

89099160-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7041307-G-C

89099160-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7041307-G-T

89099216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7041252-C-T

89099249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7041222-A-G

89099333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7041123-A-G

89099442-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7041035-G-C

89099935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7038391-A-G

89099956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7038380-A-G

89101314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7037372-T-C

89101398-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7037285-T-G

89107044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7036428-C-T

89107050-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7036422-T-A

89107078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7036393-T-C

89107241-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7036236-T-A

89107363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7036100-T-C

89107479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7036020-T-C

89107505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7035995-G-A

89107660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7035837-A-G

89107711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7035752-A-G

89107737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7035727-A-G

89107796-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7035671-A-T

89108014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7035489-T-C

89108137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7035366-A-G

89108220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7035288-C-T

89108412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7035091-A-G

89108641-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7034023-C-G

89108641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7034023-C-T

89108650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7034014-T-C

89109110-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7033565-T-G

http://identifiers.org/hco/7/GRCh38#89109330-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#7033372-A-C

89109330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7033372-A-G

89109605-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7033126-C-G

http://identifiers.org/hco/7/GRCh38#89109811-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#7032909-A-C

89110045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7032698-T-C

89110058-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7032684-T-G

89110083-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7032660-T-A

89110083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7032660-T-C

89110133-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7032609-T-G

89110197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7032544-T-C

89110297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7032483-G-A

89110456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7032325-G-A

89110936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7031896-C-T

89118242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7023450-G-A

http://identifiers.org/hco/7/GRCh38#89118479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#7023283-C-A

http://identifiers.org/hco/7/GRCh38#89118651-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#7023118-C-A

89118901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7022923-G-T

89118918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7022906-T-C

89118965-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7022860-T-G

89119013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7022820-A-G

89123121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7007826-T-C

89123136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7007811-G-A

89123193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7007741-A-G

89123264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7007669-G-T

89123291-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7007631-A-T

89123429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7007504-T-C

http://identifiers.org/hco/7/GRCh38#89123441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#7007493-C-A

89123441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7007493-C-T

89123442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7007492-G-A

89123466-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7007468-C-G

89123479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7007454-G-A

89123479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7007454-G-T

89123493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7007439-G-T

89123562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7007378-T-C

89123662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7007294-T-C

http://identifiers.org/hco/7/GRCh38#89123889-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#7007074-A-C

89123889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7007074-A-G

89123966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7007002-A-G

89124044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron_variant, undefined
orthologous variants: 7006923-C-T

89124045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron_variant, undefined
orthologous variants: 7006922-C-T

89124100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron_variant, undefined
orthologous variants: 7006867-T-C

89124158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron_variant, undefined
orthologous variants: 7006817-A-G

89124331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7006664-G-A

89124331-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7006664-G-C

89124365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7006622-G-A

89124365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7006622-G-T

89124387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7006589-C-T

89124392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7006584-G-T

89124505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7006474-G-T

89124523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7006456-A-G

89124528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7006451-A-G

89124611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7006375-T-C

89124702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7006315-G-T

89124813-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7006217-T-G

89124853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7006181-T-C

89124948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7006092-T-C

89124984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7006052-G-T

89124995-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7006041-A-T

89124996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7006040-C-T

89125058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7005991-G-A

89125058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7005991-G-T

89125392-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7005645-G-C

89126152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7005084-A-G

89126167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7005067-T-C

89126167-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7005067-T-G

89126239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7004986-A-G

89126718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7004896-C-T

http://identifiers.org/hco/7/GRCh38#89126763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#7004852-C-A

89127067-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7004557-T-A

89127067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7004557-T-C

89127077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7004548-A-G

89127077-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7004548-A-T

89127131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7004498-T-C

89127386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7004248-G-A

89127488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7004150-G-A

89127594-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7004046-G-C

89127609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7004032-A-G

89127766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7003905-G-A

89127855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7003834-A-G

89127975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7003715-T-C

89128016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7003677-G-A

89128066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7003631-T-C

89128068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7003629-G-A

89128068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7003629-G-T

89131023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7001571-C-T

89131038-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7001556-T-A

89131038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7001556-T-C

89131244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7001338-A-G

89131375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7000564-T-C

89131510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7000432-G-T

89131787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7000163-T-C

89131791-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7000159-T-G

89131962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 7000034-T-C

89132164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6999852-A-G

89132257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6999788-T-C

89132449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6999647-A-G

89132471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6999625-A-G

89132480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6999616-C-T

89132528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6999569-C-T

89132833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6999295-C-T

89133054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6999080-T-C

http://identifiers.org/hco/7/GRCh38#89133298-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6998863-A-C

89133309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6998856-G-A

89133313-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6998849-C-G

89133320-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6998842-T-A

89133344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6998819-T-C

89133391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6998776-C-T

89133414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6998762-A-G

89133447-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6998729-T-A

89133513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6998666-T-C

89133589-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6998590-C-G

89133705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6998474-A-G

89133911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6998279-G-A

89134019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6998170-T-C

89134137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6998061-C-T

89134305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6997993-A-G

89134376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6997931-G-A

89134483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6997849-G-A

89134567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6997778-G-A

89134581-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6997764-T-A

89134628-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6997734-T-A

89134691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6997675-A-G

89134867-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6997513-T-A

89134867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6997513-T-C

89145683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6995887-T-C

89145767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6995798-A-G

89145914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6995649-T-C

89145940-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6995624-T-A

89145968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6995597-A-G

89145995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6995571-A-G

89145998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6995568-C-T

89146167-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6995423-A-T

89146556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6995086-A-G

89146696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6994957-G-T

89148157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6994650-C-T

89148582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6994261-C-T

89148603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6994237-G-A

89148603-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6994237-G-C

89148701-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6994146-T-A

89148929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6993914-A-G

89148931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6993912-C-T

89148932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6993911-A-G

89148960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6993864-A-G

89148963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6993861-C-T

89149048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6993756-C-T

89149266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6993539-G-A

89149397-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6993426-C-G

89149436-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6993380-T-A

89149440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6993371-G-A

89156594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6990645-G-A

89156594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6990645-G-T

89156665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6990703-C-T

89156677-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6990716-T-A

89156936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6991007-G-A

89157009-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6991078-T-G

89157172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6991203-G-A

89157250-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6991280-A-T

89157342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6991374-C-T

89157369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6991398-G-A

89157437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6991465-G-A

89157459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6991487-A-G

89159742-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6989715-C-G

89159848-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6989609-G-C

89159849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6989608-G-A

89159988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6989483-T-C

89160201-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6988702-T-G

89160330-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6988577-T-G

89160619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6988319-C-T

89160657-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6988288-G-C

http://identifiers.org/hco/7/GRCh38#89160683-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6988264-A-C

89160812-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6988143-A-T

89160854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6988102-T-C

89160866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6988086-C-T

89161072-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6987881-T-A

89161108-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6987821-C-G

89161174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6987776-G-A

89161184-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6987763-A-T

89161185-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6987762-C-G

89161229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6987727-G-A

89161239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6987721-C-T

89161289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6987673-T-C

89161341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6987621-G-A

89161341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6987621-G-T

89161361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6987601-G-T

89161401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6987562-C-T

89161712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6987398-G-T

89161733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6987376-G-T

89163401-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6987210-T-A

89163649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6986986-G-A

89163689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6986947-A-G

89164234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6986440-T-C

89164373-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6986330-A-T

89164375-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6986328-T-G

89164395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6986311-A-G

89164407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6986297-T-C

89164528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6986190-T-C

89164581-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6986136-T-G

89164728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6986004-C-T

89165741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6985705-G-A

89165741-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6985705-G-T

89165885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6985584-A-G

89165902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6985567-A-G

89165980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6985485-A-G

89166087-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6985389-T-A

89166091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6985385-G-A

89166091-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6985385-G-T

89167565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6985204-T-C

89167573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6985196-T-C

89167591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6985175-T-C

89167593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6985173-T-C

http://identifiers.org/hco/7/GRCh38#89167655-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6985106-A-C

http://identifiers.org/hco/7/GRCh38#89167793-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6984998-A-C

89167888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6984906-C-T

89167909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6984888-G-A

89168055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6984763-A-G

89168199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6984635-T-C

http://identifiers.org/hco/7/GRCh38#89169753-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6982510-A-C

89169858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6982418-G-A

89170018-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6982245-A-T

89170063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6982196-T-C

http://identifiers.org/hco/7/GRCh38#89170068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6982191-C-A

89170068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6982191-C-T

89170096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6982177-T-C

89170793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6981549-G-A

89170793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6981549-G-T

89170894-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6981474-C-G

89170911-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6981457-C-G

89170911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6981457-C-T

89170985-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6981391-A-T

89171079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6981291-A-G

89171122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6981248-G-A

89171203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6981166-A-G

89171207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6981162-A-G

89171838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6980992-A-G

89171908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6980905-T-C

89172127-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6979166-A-T

89172153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6979140-G-A

89172165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6979130-C-T

89172253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6979051-C-T

89172257-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6979047-C-G

89172265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6979039-T-C

89172295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6979009-A-G

89172512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6978866-T-C

89172574-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6978812-C-G

89172656-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6978734-A-T

89172792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6978605-A-G

89172870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6978527-T-C

89173010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6976319-T-C

89173023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6976306-T-C

89173042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6976288-C-T

89173214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6976118-T-C

89173360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6975980-A-G

http://identifiers.org/hco/7/GRCh38#89173408-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6975933-A-C

http://identifiers.org/hco/7/GRCh38#89173411-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6975930-A-C

http://identifiers.org/hco/7/GRCh38#89173419-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6975922-A-C

89173434-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6975907-A-T

89173517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6975841-A-G

89173543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6975815-A-G

89173607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6975742-G-T

89173755-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6975545-T-A

89173755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6975545-T-C

89181794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6975370-G-T

89181870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6975296-A-G

89182025-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6975140-T-G

89182056-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6975109-T-A

89182056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6975109-T-C

89182242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6974927-G-T

http://identifiers.org/hco/7/GRCh38#89182316-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6974836-A-C

89182326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6974826-T-C

89182537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6974648-T-C

89182562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6974623-A-G

89183366-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6974589-A-T

89183425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6974539-G-A

89183425-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6974539-G-C

89183644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6974345-A-G

89183774-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6974215-T-G

89183797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6974192-C-T

89183839-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6974161-C-G

89184025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6973985-G-T

89184577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6968003-T-C

89184690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6967833-A-G

89184740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6967799-G-A

89186397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6965748-T-C

89186837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6965252-G-T

89186849-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6965227-T-G

89187039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6965034-A-G

89187061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6965012-A-G

89187103-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6964973-T-A

89187225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6964883-C-T

http://identifiers.org/hco/7/GRCh38#89187237-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6964871-A-C

89187273-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6964834-T-G

89187566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6964561-A-G

89187646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6964487-T-C

89187795-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6964318-A-T

89191539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6963892-A-G

89191874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6963597-T-C

89191898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6963573-A-G

89191966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6963467-G-A

http://identifiers.org/hco/7/GRCh38#89192061-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6963373-A-C

89192148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6963291-G-A

89192190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6963250-A-G

http://identifiers.org/hco/7/GRCh38#89197606-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6947420-A-C

89197741-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6947290-T-A

89197894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6947137-A-G

89200739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6946470-C-T

89200741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6946468-C-T

89201021-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6946226-T-A

89201678-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6945665-T-G

http://identifiers.org/hco/7/GRCh38#89201960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6945385-C-A

http://identifiers.org/hco/7/GRCh38#89202144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6945207-C-A

89202161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6945192-T-C

89202214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6945110-G-A

89202433-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6944919-T-G

89202682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6944678-A-G

89203273-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6944067-C-G

89203643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6943623-G-A

89204009-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6943251-A-T

89204072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6943186-A-G

89204072-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6943186-A-T

89204150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6943113-G-A

89204446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6942823-C-T

89204629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6942636-G-T

89204642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6942626-C-T

89204764-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6942502-T-G

89209170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6936251-C-T

89209684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6935761-T-C

http://identifiers.org/hco/7/GRCh38#89210289-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6935489-A-C

89212916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6932345-G-A

http://identifiers.org/hco/7/GRCh38#89213584-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6931811-A-C

http://identifiers.org/hco/7/GRCh38#89213728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6931740-C-A

89213784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6931677-A-G

89213824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6931640-A-G

http://identifiers.org/hco/7/GRCh38#89214022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6931444-C-A

89214022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6931444-C-T

89214023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6931443-G-A

89214023-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6931443-G-C

89214070-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6931398-T-G

89215141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6928278-G-A

89215207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6928212-T-C

89215278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6928143-G-A

89215348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6928074-A-G

89215439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6927999-T-C

89215456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6927983-A-G

89215461-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6927978-T-A

89216323-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6927835-A-T

89216343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6927813-G-A

89216454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6927703-T-C

89216511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6927651-T-C

89216535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6927625-T-C

89216535-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6927625-T-G

89216607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6927558-T-C

http://identifiers.org/hco/7/GRCh38#89216986-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6927309-A-C

89217100-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6927197-C-G

89217100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6927197-C-T

89217287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6927053-C-T

89217600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6926923-A-G

89217630-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6926893-A-T

89217891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6926681-C-T

89218012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6926665-G-A

89218012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6926665-G-T

89218034-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6926643-T-A

89218092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6926579-T-C

89218101-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6926570-T-G

89218122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6926551-G-A

89218203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 6926470-G-A

89218203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 6926470-G-T

89218336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6926337-A-G

89218336-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6926337-A-T

89218542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6926132-G-A

89218542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6926132-G-T

http://identifiers.org/hco/7/GRCh38#89219613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6924084-C-A

89219613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6924084-C-T

http://identifiers.org/hco/7/GRCh38#89219678-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6924011-A-C

89219685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6924004-G-A

89219788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6923919-A-G

89219830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6923889-T-C

89220202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6923866-A-G

89220246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6923822-T-C

89220349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6923724-C-T

89220520-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6923569-T-A

89220535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6923554-A-G

http://identifiers.org/hco/7/GRCh38#89220626-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6923466-A-C

89220626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6923466-A-G

89220661-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6923435-T-A

89220661-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6923435-T-G

89220673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6923427-A-G

http://identifiers.org/hco/7/GRCh38#89220731-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6923389-A-C

89220795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6923339-G-T

http://identifiers.org/hco/7/GRCh38#89220841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6923292-C-A

89220983-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6923141-T-A

89220983-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6923141-T-G

http://identifiers.org/hco/7/GRCh38#89221040-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6923085-A-C

89221411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6922784-T-C

http://identifiers.org/hco/7/GRCh38#89221876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6922449-C-A

89221898-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6922422-A-T

89221938-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6922380-T-A

89221938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6922380-T-C

89222163-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6922152-G-C

89222429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6921920-A-G

89222741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6921620-A-G

89222745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6921615-G-T

89222887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6921482-T-C

http://identifiers.org/hco/7/GRCh38#89222954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6921416-C-A

http://identifiers.org/hco/7/GRCh38#89222958-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6921412-A-C

89223069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6921251-T-C

89223489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6920814-C-T

89223661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6920534-G-A

89223675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6920520-C-T

89223790-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6920402-T-A

89223831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6920360-T-C

89223856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6920334-T-C

89223940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6920250-T-C

89223970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6920221-T-C

89224182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6920035-A-G

http://identifiers.org/hco/7/GRCh38#89224202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6920015-C-A

http://identifiers.org/hco/7/GRCh38#89224223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6919996-C-A

89224249-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6919970-C-G

89224388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6919835-T-C

89224396-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6919827-C-G

89224526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6919654-A-G

http://identifiers.org/hco/7/GRCh38#89224683-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6919321-A-C

89224683-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6919321-A-T

89224757-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6919236-T-A

89224759-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6919234-T-A

89224759-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6919234-T-G

89224771-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6919222-T-A

89224793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6919181-A-G

89225050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6918981-T-C

89225050-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6918981-T-G

89225226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6918796-A-G

89225233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6918789-A-G

89225261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6918762-T-C

89225313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6918721-G-A

89225315-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6918719-C-G

89225574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6910739-C-T

http://identifiers.org/hco/7/GRCh38#89225841-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6910521-A-C

89225895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6910463-G-A

89226083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6910303-A-G

http://identifiers.org/hco/7/GRCh38#89226106-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6910282-A-C

89226283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6910131-A-G

89226505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6909919-C-T

89226632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6909759-T-C

http://identifiers.org/hco/7/GRCh38#89226711-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6909599-A-C

89226826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6909487-G-A

89227002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6909310-A-G

89227121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6909192-C-T

89227125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6909188-G-A

89227322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6908945-T-C

89227499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6908805-A-G

89241348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6895723-T-C

89241533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6895540-G-T

89242120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6895017-T-C

http://identifiers.org/hco/7/GRCh38#89242657-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6892080-A-C

89243165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6888461-A-G

89243490-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6888143-A-T

89243651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6887986-A-G

89243865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6887830-G-T

89243991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6887710-A-G

89244005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6887696-A-G

89244005-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6887696-A-T

89244045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6887660-C-T

89244091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6887617-G-A

89244130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6887576-G-A

89244249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6887466-T-C

89244349-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6887365-G-C

89257347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6886325-A-G

89257374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6886298-C-T

89257899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6886191-C-T

89257901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6886189-G-A

89262197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6885521-T-C

89262881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6883958-A-G

89262956-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6883868-T-A

89263075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6883642-A-G

89263306-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6883436-C-G

89263306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6883436-C-T

89263904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6879040-A-G

89264079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6878839-A-G

89264176-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6878775-T-G

89264238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6878716-C-T

89264324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6878655-A-G

89264348-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6878636-C-G

89264365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6878617-A-G

89264652-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6878291-T-A

89264727-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6878244-A-T

89265020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6877950-G-T

89265058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6877770-A-G

89265213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6877597-G-T

89265264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6877560-C-T

89265277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6877547-T-C

89265279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6877545-T-C

89265283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6877541-T-C

89265285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6877539-T-C

89265287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6877537-T-C

89265288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6877536-G-A

89265289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6877535-T-C

89265640-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6877332-C-G

89265728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6877242-A-G

89265794-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6877175-C-G

http://identifiers.org/hco/7/GRCh38#89266070-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6876909-A-C

http://identifiers.org/hco/7/GRCh38#89266188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6876791-C-A

89266323-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6876663-G-C

89266323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6876663-G-T

89266433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6876571-T-C

http://identifiers.org/hco/7/GRCh38#89266755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6876123-C-A

89266885-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6875982-G-C

89266887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6875980-G-A

89266893-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6875974-C-G

89266897-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6875970-G-C

89266901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6875966-G-A

89266920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6875919-G-T

89267162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6875670-C-T

89267176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6875661-A-G

89267324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6875519-T-C

http://identifiers.org/hco/7/GRCh38#89267364-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6875475-A-C

http://identifiers.org/hco/7/GRCh38#89267451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6875396-C-A

89267972-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6875200-C-G

89268079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6875102-C-T

http://identifiers.org/hco/7/GRCh38#89268080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6875101-C-A

89268080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6875101-C-T

89268175-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6875017-C-G

89271948-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6874119-A-T

89272019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6874053-A-G

89272175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6873921-G-A

89272260-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6873828-C-G

89272260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6873828-C-T

89272423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6873689-T-C

89272547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6873578-G-T

89272559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6873573-A-G

89272632-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6873496-A-T

89272662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6873371-T-C

http://identifiers.org/hco/7/GRCh38#89272790-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6873049-A-C

89272790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6873049-A-G

89272836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6872993-C-T

89272915-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6872918-T-A

89272973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6872860-G-A

89273083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6872768-A-G

http://identifiers.org/hco/7/GRCh38#89273115-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6872740-A-C

89273168-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6872705-T-A

89273244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6872632-C-T

89273313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6872563-A-G

89273704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6872194-T-C

89273729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6872169-T-C

89273746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6872152-T-C

89273821-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6872078-C-G

89273863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6872017-G-A

89274016-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6871890-G-C

89274016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6871890-G-T

http://identifiers.org/hco/7/GRCh38#89274024-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6871882-A-C

89274024-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6871882-A-T

89276538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6869359-A-G

89276791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6869170-T-C

89277023-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6868960-T-G

89277056-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6868928-T-G

http://identifiers.org/hco/7/GRCh38#89298891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6864971-C-A

89298907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6864955-G-A

89299820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6863892-T-C

89299949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6863668-G-A

89299966-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6863644-T-A

89299966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6863644-T-C

http://identifiers.org/hco/7/GRCh38#89300537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6863085-C-A

89300744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6862672-A-G

89300744-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6862672-A-T

89300875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6862552-G-A

89301129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6862348-G-A

89301129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6862348-G-T

89301141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6862334-T-C

89301191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6862270-A-G

89301417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6861637-A-G

89301657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6861431-C-T

89301707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6861378-T-C

89301876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6861225-A-G

89302132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6860976-A-G

http://identifiers.org/hco/7/GRCh38#89302344-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6860691-A-C

89302344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6860691-A-G

89302347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6860688-G-A

89302856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6860193-A-G

89303055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6859832-G-A

89303095-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6859796-C-G

89304969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6859154-A-G

http://identifiers.org/hco/7/GRCh38#89305598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6858182-C-A

89305598-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6858182-C-G

89305624-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6858166-T-G

http://identifiers.org/hco/7/GRCh38#89305656-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6858134-A-C

89305767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6857146-A-G

89305829-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6857075-A-T

89305883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6857026-G-T

89306036-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6856869-T-G

89306532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6856414-A-G

89306613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6856352-A-G

89306857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6851446-G-T

89306964-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6851339-A-T

89307159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6851148-A-G

89307455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6850925-A-G

89307490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6850888-T-C

89307551-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6850810-T-G

http://identifiers.org/hco/7/GRCh38#89307690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6850665-C-A

89307690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6850665-C-T

89307704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6850651-T-C

89307718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6850641-A-G

89307789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6850584-T-C

89308101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6850279-G-A

89308151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6850233-G-A

89308289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6849500-A-G

89308361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6849428-A-G

89308475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6849303-C-T

89308581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6849201-C-T

89308831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6848962-G-T

89308869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6848923-G-A

http://identifiers.org/hco/7/GRCh38#89308972-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6848827-A-C

89310032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6848314-G-A

89310052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6848296-T-C

89310102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6848241-A-G

http://identifiers.org/hco/7/GRCh38#89310154-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6848176-A-C

89310154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6848176-A-G

89310155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6848175-T-C

89310197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6848133-C-T

89310398-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6847935-C-G

89311217-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6847100-T-A

89311217-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6847100-T-G

89311983-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6846247-T-A

89312222-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6845049-C-G

89312366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6844894-A-G

http://identifiers.org/hco/7/GRCh38#89312552-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6844706-A-C

89312552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6844706-A-G

http://identifiers.org/hco/7/GRCh38#89312586-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6844672-A-C

89312904-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6844493-G-C

89312908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6844485-A-G

http://identifiers.org/hco/7/GRCh38#89312934-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6844450-A-C

89313280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6844170-C-T

89313326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6844123-A-G

http://identifiers.org/hco/7/GRCh38#89313418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6844031-C-A

89313418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6844031-C-T

89313471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6844003-C-T

http://identifiers.org/hco/7/GRCh38#89313707-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6843773-A-C

89313863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6843619-C-T

89313963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6843522-A-G

89313975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6843507-G-A

http://identifiers.org/hco/7/GRCh38#89313996-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6843486-A-C

89314249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6842894-C-T

http://identifiers.org/hco/7/GRCh38#89314292-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6842858-A-C

89314292-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6842858-A-T

http://identifiers.org/hco/7/GRCh38#89314376-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6842770-A-C

89314548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6842625-A-G

89314599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6842565-C-T

89315611-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6839671-T-G

89315654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6839629-G-A

89315778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6839523-T-C

89317277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6839176-G-T

89317279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6839174-G-A

89317971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6838677-A-G

89323895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6833143-A-G

89323898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6833140-G-A

89323898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6833140-G-T

89325560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6829702-A-G

http://identifiers.org/hco/7/GRCh38#89325801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6829510-C-A

89325987-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6829339-T-A

89326002-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6829324-C-G

89326002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6829324-C-T

89326792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6829093-C-T

89326850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6829042-A-G

89326896-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6829003-T-A

89326931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6828968-C-T

89326937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6828962-G-A

89327174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6828722-G-A

89327179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6828717-A-G

89327284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6828621-G-A

89327313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6828592-A-G

http://identifiers.org/hco/7/GRCh38#89327318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6828587-C-A

89327318-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6828587-C-G

89327318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6828587-C-T

89327337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 6828568-T-C

89327395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: missense variant
orthologous variants: 6828511-T-C

89327444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: missense variant
orthologous variants: 6828462-A-G

89327530-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6828376-T-G

89327548-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6828349-T-A

89327678-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6828218-C-G

89327678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6828218-C-T

89327712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6828183-A-G

89327822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6827626-G-T

89327982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6827466-C-T

http://identifiers.org/hco/7/GRCh38#89328038-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6827410-A-C

89328055-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6827393-C-G

89328073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6827375-T-C

89328158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6827290-T-C

89328371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6827085-T-C

89328406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6827059-A-G

89328563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6826913-A-G

89328586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6826895-T-C

89328670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6826807-A-G

89328719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6826756-C-T

89328876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6826593-T-C

89328879-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6826590-C-G

89328964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6826542-T-C

89328976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6826532-T-C

89329024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6826485-A-G

89329056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6826453-A-G

89329218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6826325-A-G

89329259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6826284-A-G

89329283-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6826263-T-A

89329283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6826263-T-C

89329283-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6826263-T-G

http://identifiers.org/hco/7/GRCh38#89329287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6826259-C-A

89329287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6826259-C-T

89329394-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6826169-C-G

89329494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6825941-T-C

89329730-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6825707-T-A

89329765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6825674-T-C

89330140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6825369-G-T

89331152-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6824822-T-G

89331262-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6824708-G-C

89331426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6824575-A-G

89331463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6824525-G-A

89331476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6824508-A-G

89331491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6824490-C-T

89331594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6824394-G-A

http://identifiers.org/hco/7/GRCh38#89331595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6824393-C-A

89331809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6824177-T-C

89332345-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6823613-T-A

89332345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6823613-T-C

89332345-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6823613-T-G

89332375-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6823587-C-G

89332381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6823581-A-G

89332388-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6823568-G-C

89332425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6823532-A-G

89332520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6823456-G-A

http://identifiers.org/hco/7/GRCh38#89332537-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6823434-A-C

89332568-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6823409-G-C

89332568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6823409-G-T

http://identifiers.org/hco/7/GRCh38#89332574-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6823403-A-C

89332587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6823386-A-G

http://identifiers.org/hco/7/GRCh38#89332630-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6823352-A-C

89332727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6823264-A-G

89332744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6823247-A-G

89332826-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6823178-T-A

89332998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6823040-T-C

89333244-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: intron variant
orthologous variants: 6822790-A-T

89333476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: missense variant
orthologous variants: 6822563-C-T

89333487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: missense variant
orthologous variants: 6822555-A-G

89333492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: synonymous variant
orthologous variants: 6822550-A-G

http://identifiers.org/hco/7/GRCh38#89333791-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6822251-A-C

89333894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: synonymous variant
orthologous variants: 6822154-A-G

89333934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: missense variant
orthologous variants: 6822114-A-G

89333985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: missense variant
orthologous variants: 6822063-G-T

89334009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: missense variant
orthologous variants: 6822039-A-G

89334047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: synonymous variant
orthologous variants: 6822001-T-C

89334063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: missense variant
orthologous variants: 6821985-T-C

89334063-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: missense variant
orthologous variants: 6821985-T-G

89334132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: synonymous variant
orthologous variants: 6821916-C-T

http://identifiers.org/hco/7/GRCh38#89334191-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6821857-A-C

89334249-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: missense variant
orthologous variants: 6821799-A-T

http://identifiers.org/hco/7/GRCh38#89334250-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6821798-A-C

89334250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: missense variant
orthologous variants: 6821798-A-G

89334266-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: synonymous variant
orthologous variants: 6821782-A-T

89334402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: missense variant
orthologous variants: 6821646-G-A

89334504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: synonymous variant
orthologous variants: 6821544-T-C

89334674-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: missense variant
orthologous variants: 6821377-T-G

89334875-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: missense variant
orthologous variants: 6821179-C-G

http://identifiers.org/hco/7/GRCh38#89334912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6821142-C-A

89334915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: missense variant
orthologous variants: 6821139-C-T

89334990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: missense variant
orthologous variants: 6821064-G-T

http://identifiers.org/hco/7/GRCh38#89335023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6821031-C-A

89335154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: synonymous variant
orthologous variants: 6820900-T-C

89335155-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: missense variant
orthologous variants: 6820899-A-T

89335196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: synonymous variant
orthologous variants: 6820858-T-C

89335432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: missense variant
orthologous variants: 6820625-T-C

89335488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: missense variant
orthologous variants: 6820569-T-C

89335493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: synonymous variant
orthologous variants: 6820564-T-C

89335493-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: synonymous variant
orthologous variants: 6820564-T-G

http://identifiers.org/hco/7/GRCh38#89335574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: stop gained
orthologous variants: http://identifiers.org/mco/5/GRCm39#6820483-C-A

89335574-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: stop gained
orthologous variants: 6820483-C-G

89335574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: synonymous variant
orthologous variants: 6820483-C-T

89335663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: missense variant
orthologous variants: 6820394-G-A

89335809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: missense variant
orthologous variants: 6820248-A-G

89335812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: missense variant
orthologous variants: 6820245-G-A

89335844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: synonymous variant
orthologous variants: 6820213-A-G

89335873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: missense variant
orthologous variants: 6820184-C-T

89335957-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: missense variant
orthologous variants: 6820100-A-T

http://identifiers.org/hco/7/GRCh38#89336125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6819932-C-A

89336125-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: missense variant
orthologous variants: 6819932-C-G

89336126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: synonymous variant
orthologous variants: 6819931-A-G

89336232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: missense variant
orthologous variants: 6819825-G-A

89336232-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: missense variant
orthologous variants: 6819825-G-C

89336232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: missense variant
orthologous variants: 6819825-G-T

89336309-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: missense variant
orthologous variants: 6819748-T-A

89336309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: synonymous variant
orthologous variants: 6819748-T-C

89336345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: synonymous variant
orthologous variants: 6819712-T-C

89336387-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: stop gained
orthologous variants: 6819670-T-A

89336887-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: missense variant
orthologous variants: 6819173-C-G

89336887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: missense variant
orthologous variants: 6819173-C-T

89336899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: missense variant
orthologous variants: 6819161-C-T

89337115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: 3 prime UTR variant
orthologous variants: 6818941-A-G

89337115-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: 3 prime UTR variant
orthologous variants: 6818941-A-T

http://identifiers.org/hco/7/GRCh38#89337118-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6818938-A-C

89337390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: 3 prime UTR variant
orthologous variants: 6818686-C-T

89337621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: 3 prime UTR variant
orthologous variants: 6818455-T-C

http://identifiers.org/hco/7/GRCh38#89337828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6818264-C-A

http://identifiers.org/hco/7/GRCh38#89338177-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6817978-A-C

89338259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21958
most severe consequence: 3 prime UTR variant
orthologous variants: 6817905-C-T