31318316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: missense variant
orthologous variants: 20444090-T-C

31318344-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: missense variant
orthologous variants: 20444118-T-G

http://identifiers.org/hco/18/GRCh38#31318367-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20444141-A-C

31318367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20444141-A-G

http://identifiers.org/hco/18/GRCh38#31318375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20444151-C-A

31318375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20444151-C-T

http://identifiers.org/hco/18/GRCh38#31318403-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20444181-A-C

31318474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20444251-A-G

31318474-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20444251-A-T

31318476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20444254-G-A

31318476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20444254-G-T

31318560-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20444334-T-G

31318591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20444363-T-C

31318629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20444401-T-C

31318663-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20444430-C-G

31318796-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20444567-T-G

31318798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20444569-A-G

31318808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20444579-G-A

http://identifiers.org/hco/18/GRCh38#31318836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20444607-C-A

31318857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20444635-T-C

31318947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20444723-C-T

31318987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20444765-T-C

31319191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20444942-C-T

31319215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20444967-T-C

31319248-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20445000-A-T

31319330-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20445074-T-A

31319569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20445401-G-A

31319672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20445511-A-G

31319797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20445643-A-G

31319906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20445763-G-T

31320296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20446343-A-G

31320375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20446422-C-T

31320398-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20446445-T-G

31320589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20446637-T-C

31320654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20446769-A-G

31320748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20446946-A-G

31320870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20447059-T-C

31321069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20447412-T-C

31321076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20447419-A-G

31321162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20447503-G-A

31321190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20447531-G-A

31321192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20447533-G-A

31321245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20447548-A-G

31321303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20447607-T-C

http://identifiers.org/hco/18/GRCh38#31321326-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20447630-A-C

31321381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20447682-T-C

31321451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20447727-G-T

31321530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20447800-T-C

31321570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20447839-G-A

31321570-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20447839-G-C

31321570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20447839-G-T

31321604-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20447873-G-C

31321622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20447891-G-A

31321655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20447925-C-T

31321805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20448070-T-C

31321818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20448083-C-T

31321838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20448099-C-T

31321966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20448226-G-A

31322142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20448399-C-T

31322274-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20448530-A-T

31322285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20448541-C-T

31322594-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20449053-T-A

31322683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20449176-G-A

31322837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20449268-T-C

http://identifiers.org/hco/18/GRCh38#31322845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20449277-C-A

31322845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20449277-C-T

31322861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20449293-C-T

31322897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20449310-A-G

31322912-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20449325-A-T

31322918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20449331-G-A

31322950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20449360-C-T

31322970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20449373-C-T

31323016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20449414-G-A

31323085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20449482-C-T

31323096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20449493-G-A

http://identifiers.org/hco/18/GRCh38#31323148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20449528-C-A

31323185-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20449563-T-A

31323213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20449585-C-T

31323334-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20449685-T-A

http://identifiers.org/hco/18/GRCh38#31323566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20449820-C-A

31323605-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20449855-T-A

31323700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20449936-G-A

31323700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20449936-G-T

31324027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20450225-C-T

http://identifiers.org/hco/18/GRCh38#31324055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20450235-C-A

31324140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20450262-C-T

31324224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20450288-C-T

31324329-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20450299-A-T

31324403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20450359-G-A

31324429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20450387-A-G

31324473-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20450431-T-A

31324535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20450461-A-G

31324559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20450473-T-C

31325322-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20451603-G-C

31325464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20451739-G-A

31325874-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20452467-T-A

31325904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20452496-C-T

31326072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20452636-C-T

31326431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20453156-T-C

31326466-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20453199-A-T

31326623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 20453394-T-C

31326623-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 20453394-T-G

31326735-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20453851-A-T

31326741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20453857-T-C

31326767-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20453878-T-G

31326779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20453890-A-G

31326780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20453891-T-C

31326823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20453936-A-G

31326827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20453940-A-G

http://identifiers.org/hco/18/GRCh38#31326848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20453961-C-A

31326874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 20453981-G-A

31326874-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 20453981-G-C

31326882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: synonymous variant
orthologous variants: 20453989-T-C

31326898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: missense variant
orthologous variants: 20454005-G-A

31326898-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: missense variant
orthologous variants: 20454005-G-C

31326957-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: synonymous variant
orthologous variants: 20454064-A-T

31327053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20454159-G-A

http://identifiers.org/hco/18/GRCh38#31327096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20454206-C-A

31327096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20454206-C-T

http://identifiers.org/hco/18/GRCh38#31327123-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20454234-A-C

31327123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20454234-A-G

31327136-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20454243-A-T

31327149-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20454256-T-A

31327149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20454256-T-C

31327176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20454285-T-C

http://identifiers.org/hco/18/GRCh38#31327229-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20454338-A-C

http://identifiers.org/hco/18/GRCh38#31327304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20454398-C-A

31327378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20454460-G-T

31327387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20454467-T-C

31327391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20454471-C-T

31327404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20454484-C-T

31327472-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20454551-A-T

31327622-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20454707-G-T

31327677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20454751-C-T

31327790-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20454863-T-G

31327914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20454983-T-C

31328002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20455062-A-G

31328039-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20455098-G-C

31328039-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20455098-G-T

http://identifiers.org/hco/18/GRCh38#31328050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20455109-C-A

31328050-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20455109-C-G

31328051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20455110-T-C

31328109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20455170-A-G

31328124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20455189-G-A

31328124-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20455189-G-T

http://identifiers.org/hco/18/GRCh38#31328126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20455191-C-A

31328126-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20455191-C-G

31328126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20455191-C-T

31328138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20455201-A-G

31328139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20455202-T-C

31328139-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20455202-T-G

31328159-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20455225-C-G

31328159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20455225-C-T

31328206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: synonymous variant
orthologous variants: 20455271-T-C

31328212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: synonymous variant
orthologous variants: 20455277-C-T

31328236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: synonymous variant
orthologous variants: 20455301-T-C

31328366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20455431-A-G

31328373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20455438-T-C

31328374-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20455439-T-A

http://identifiers.org/hco/18/GRCh38#31328375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20455440-C-A

31328435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20455495-G-A

31328435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20455495-G-T

http://identifiers.org/hco/18/GRCh38#31328439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20455499-C-A

31328439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20455499-C-T

31328444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20455504-T-C

31328448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20455508-G-A

31328448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20455508-G-T

http://identifiers.org/hco/18/GRCh38#31328449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20455509-C-A

31328449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20455509-C-T

31328468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20455528-A-G

31328468-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20455528-A-T

http://identifiers.org/hco/18/GRCh38#31328484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20455539-C-A

31328484-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20455539-C-G

31328484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20455539-C-T

http://identifiers.org/hco/18/GRCh38#31328500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20455550-C-A

31328500-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20455550-C-G

31328522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20455568-T-C

31328535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20455581-T-C

http://identifiers.org/hco/18/GRCh38#31328568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20455612-C-A

31328570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20455613-T-C

31328829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20455862-T-C

31328850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20455872-C-T

31328981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20456006-G-A

http://identifiers.org/hco/18/GRCh38#31329033-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20456040-A-C

31329042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20456049-A-G

http://identifiers.org/hco/18/GRCh38#31329212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20456214-C-A

31329252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20456253-C-T

31329274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20456279-A-G

31329298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20456304-G-A

31329298-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20456304-G-C

31329861-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20456912-A-T

31329875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20456980-T-C

31329901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: stop gained
orthologous variants: 20457010-C-T

31331044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20459037-A-G

31331187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20459175-G-A

31331234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20459247-A-G

31331278-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20459287-G-C

31331338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20459347-T-C

31331345-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20459356-T-G

31331604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20459609-G-A

31331604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20459609-G-T

31331634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20459615-G-A

31331634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20459615-G-T

31331638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20459619-A-G

31331643-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20459624-C-G

31331643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20459624-C-T

http://identifiers.org/hco/18/GRCh38#31331645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20459626-C-A

31331645-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20459626-C-G

31331645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20459626-C-T

http://identifiers.org/hco/18/GRCh38#31331682-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20459659-A-C

31331729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: synonymous variant
orthologous variants: 20459706-T-C

31331886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20459863-G-A

31331921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20459895-G-A

31331921-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20459895-G-C

31332876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20460648-G-T

31332923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20460695-G-A

31332991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20460740-G-A

31333009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20460758-A-G

31333134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20460861-G-A

31333135-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20460862-T-G

31333169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20460895-C-T

31333212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20460930-T-C

31333275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20460968-T-C

31333306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20460999-A-G

31333337-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20461030-T-G

31333354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20461047-T-C

31333389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20461080-G-T

31333417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20461108-G-A

31333427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20461118-G-A

31333469-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20461179-A-T

http://identifiers.org/hco/18/GRCh38#31333499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20461209-C-A

31333499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20461209-C-T

31333538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20461249-G-T

31333796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20461509-A-G

31333812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20461525-T-C

31333812-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20461525-T-G

http://identifiers.org/hco/18/GRCh38#31333841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20461553-C-A

31333841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20461553-C-T

31333845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20461557-T-C

http://identifiers.org/hco/18/GRCh38#31333846-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20461558-A-C

31333846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20461558-A-G

31333846-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20461558-A-T

31333852-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20461564-T-G

31333853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20461565-T-C

31333885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20461601-G-A

31333885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20461601-G-T

31333905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20461618-A-G

31333911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20461624-A-G

http://identifiers.org/hco/18/GRCh38#31333947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20461659-C-A

31333947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20461659-C-T

31334026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: missense variant
orthologous variants: 20461729-G-A

31334027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: missense variant
orthologous variants: 20461730-A-G

31334040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: synonymous variant
orthologous variants: 20461743-T-C

31334217-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20461920-T-A

31334231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20461934-T-C

http://identifiers.org/hco/18/GRCh38#31334238-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20461941-A-C

31334275-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20461976-T-A

31334275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20461976-T-C

31334275-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20461976-T-G

31334296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20461995-G-A

31334296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20461995-G-T

31334303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20462002-G-T

31334317-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20462016-T-A

31334327-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20462026-T-A

31334327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20462026-T-C

31334337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20462036-T-C

31334337-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20462036-T-G

31334427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20462120-A-G

31334427-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20462120-A-T

31334664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20462623-T-C

31334977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20462860-A-G

31335040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20463037-G-T

31335058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20463055-G-A

31335854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20464003-T-C

31335855-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20464004-A-T

31335942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20464090-A-G

31336054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20464190-T-C

http://identifiers.org/hco/18/GRCh38#31336147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20464297-C-A

31336149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20464299-A-G

31336205-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20464356-A-T

31336215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20464366-G-A

31336215-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20464366-G-C

31336215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20464366-G-T

31336230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20464381-T-C

31336297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20464460-T-C

31336323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20464481-T-C

31336324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20464482-A-G

31336345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20464503-A-G

http://identifiers.org/hco/18/GRCh38#31338342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20465103-C-A

31338342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: synonymous variant
orthologous variants: 20465103-C-T

31338345-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: synonymous variant
orthologous variants: 20465106-G-C

31338431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: missense variant
orthologous variants: 20465192-A-G

31338482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20465233-T-C

31338648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20465411-A-G

31338720-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20465538-T-A

31338925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20465725-A-G

31338925-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20465725-A-T

31338944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20465748-A-G

31338979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20465783-G-A

31339044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20465828-A-G

http://identifiers.org/hco/18/GRCh38#31339067-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20465851-A-C

31339135-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20465917-T-A

31339201-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20465982-T-G

31339239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20466020-G-A

http://identifiers.org/hco/18/GRCh38#31339295-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20466091-A-C

31339299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20466095-A-G

31339381-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20466170-A-T

31339395-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20466184-G-C

http://identifiers.org/hco/18/GRCh38#31339484-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20466271-A-C

31339610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20466390-G-A

31339932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: missense variant
orthologous variants: 20466779-C-T

31341454-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20467729-T-A

31341538-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20467815-T-G

31341598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20467874-G-A

31341855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20468099-C-T

http://identifiers.org/hco/18/GRCh38#31343276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20468795-C-A

31343276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20468795-C-T

http://identifiers.org/hco/18/GRCh38#31343299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20468818-C-A

31343319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20468838-T-C

31343319-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20468838-T-G

31343320-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20468839-G-C

31343320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20468839-G-T

31343331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20468854-A-G

31343348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20468871-G-A

31343348-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron variant
orthologous variants: 20468871-G-C

31343386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20468903-A-G

31343386-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20468903-A-T

31343399-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20468916-T-A

31343434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20468941-A-G

31343439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20468946-T-C

31343445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 20468952-A-G

31343445-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 20468952-A-T

31343556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 20469065-A-G

http://identifiers.org/hco/18/GRCh38#31343580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20469092-C-A

31343583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 20469095-G-T

31343629-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20469574-T-A

31343633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20469578-T-C

31343633-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20469578-T-G

http://identifiers.org/hco/18/GRCh38#31343642-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20469587-A-C

31343642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20469587-A-G

31343700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 20469634-T-C

31343704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 20469638-G-A

31343704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 20469638-G-T

31343720-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20469653-A-T

31343724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20469657-A-G

31343828-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20469758-G-T

http://identifiers.org/hco/18/GRCh38#31343896-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20469816-C-A

31343901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20469821-G-A

31343922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 20469844-T-C

31343983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20469908-A-G

31344016-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20469941-T-A

31344061-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20469983-T-A

31344253-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20470177-G-C

31344277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20470201-T-C

31344468-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20470343-G-C

31344483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20470357-A-G

31344786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20470632-C-T

31344858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20470716-A-G

31344988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20470884-T-C

31345022-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20470918-C-G

31345032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20470928-G-A

31345058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20470956-A-G

http://identifiers.org/hco/18/GRCh38#31345134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20471034-C-A

31345216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20471111-G-T

31345263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20471137-C-T

31345356-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20471177-A-T

31345497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20471237-T-C

31345544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20471283-T-C

31345573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20471312-T-C

31345619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20471358-T-C

31345721-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20471454-A-T

31345756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20471484-T-C

31345862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20471584-T-C

31345881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20471604-T-C

31345894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20471612-A-G

31345894-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20471612-A-T

31345902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20471620-G-A

31345915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20471633-A-G

31345918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20471636-A-G

http://identifiers.org/hco/18/GRCh38#31345934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20471639-C-A

31345934-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20471639-C-G

31345934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20471639-C-T

31345951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20471656-G-A

31345951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20471656-G-T

31345966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20471671-A-G

31346063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 20471768-A-G

31346168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 20471873-T-C

http://identifiers.org/hco/18/GRCh38#31346226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20471931-C-A

31346226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20471931-C-T

31346235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20471940-T-C

http://identifiers.org/hco/18/GRCh38#31346258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20471952-C-A

http://identifiers.org/hco/18/GRCh38#31346270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20471964-C-A

31346277-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20471971-G-C

31346277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20471971-G-T

http://identifiers.org/hco/18/GRCh38#31346328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20471990-C-A

31346343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20472003-G-A

31346352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20472012-T-C

http://identifiers.org/hco/18/GRCh38#31346390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20472050-C-A

31346401-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20472061-C-G

31346571-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20472222-G-C

31346574-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20472225-T-A

31346634-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20472291-T-A

http://identifiers.org/hco/18/GRCh38#31346635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20472292-C-A

31346639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20472296-C-T

http://identifiers.org/hco/18/GRCh38#31346689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20472345-C-A

31346689-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20472345-C-G

31346727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20472377-T-C

http://identifiers.org/hco/18/GRCh38#31346749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20472400-C-A

31346749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20472400-C-T

31346751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20472402-T-C

31346755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20472406-T-C

http://identifiers.org/hco/18/GRCh38#31346801-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20472449-A-C

31346825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20472473-T-C

31354044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20472694-A-G

http://identifiers.org/hco/18/GRCh38#31354073-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20472724-A-C

31354157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20472986-G-A

31354157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20472986-G-T

31354159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20472988-A-G

31354159-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20472988-A-T

31354166-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20472995-G-C

31354168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20472999-A-G

31354168-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20472999-A-T

31354169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20473000-T-C

http://identifiers.org/hco/18/GRCh38#31354222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20473023-C-A

31354222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20473023-C-T

31354229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20473030-T-C

31354229-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20473030-T-G

31354276-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20473061-C-G

31354276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20473061-C-T

31354285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20473070-C-T

http://identifiers.org/hco/18/GRCh38#31354491-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20473277-A-C

http://identifiers.org/hco/18/GRCh38#31354507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20473299-C-A

31354507-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20473299-C-G

31354513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20473305-C-T

31354542-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 20473334-A-T

http://identifiers.org/hco/18/GRCh38#31354584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20473373-C-A

31354584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 20473373-C-T

31354593-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20473382-C-G

31354610-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20473399-C-G

31354610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20473399-C-T

31354629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 20473418-G-A

31354629-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20473418-G-C

31354688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20473477-G-A

31354688-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20473477-G-C

31354695-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 20473484-T-G

31354707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 20473496-G-A

31354750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20473539-C-T

http://identifiers.org/hco/18/GRCh38#31354764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20473553-C-A

31354764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 20473553-C-T

31354859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20473648-A-G

31354887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 20473676-G-A

31354923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 20473712-G-A

31354923-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 20473712-G-C

31354940-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20473729-G-C

31355022-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20473811-G-C

http://identifiers.org/hco/18/GRCh38#31355131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20473926-C-A

31355145-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20473940-C-G

31355191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20473950-G-A

31355191-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20473950-G-C

31355191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20473950-G-T

http://identifiers.org/hco/18/GRCh38#31355208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20473967-C-A

31355208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 20473967-C-T

31355292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 20474048-T-C

31355292-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 20474048-T-G

31355328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 20474084-C-T

31355329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20474085-G-A

31355329-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20474085-G-C

http://identifiers.org/hco/18/GRCh38#31355359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20474115-C-A

31355509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20474261-G-A

31355509-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20474261-G-C

31355514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20474266-G-T

31355646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20474473-T-C

31355663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20474490-C-T

31355856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20474658-A-G

31355857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20474659-G-A

31355857-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20474659-G-C

http://identifiers.org/hco/18/GRCh38#31355860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20474662-C-A

31355861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20474663-A-G

31355882-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20474684-C-G

31355934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20474744-G-A

31355991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20474799-C-T

http://identifiers.org/hco/18/GRCh38#31356021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20474818-C-A

http://identifiers.org/hco/18/GRCh38#31356062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20474859-C-A

31356062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20474859-C-T

31356172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20474955-G-T

http://identifiers.org/hco/18/GRCh38#31356234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20474992-C-A

31356305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20475056-T-C

31356313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20475064-A-G

31356336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20475087-A-G

31356369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20475120-G-A

http://identifiers.org/hco/18/GRCh38#31356372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20475123-C-A

31356375-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20475126-T-A

31356375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20475126-T-C

31356441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20475176-G-A

http://identifiers.org/hco/18/GRCh38#31356452-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20475193-A-C

http://identifiers.org/hco/18/GRCh38#31356518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20475260-C-A

31356518-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20475260-C-G

31356549-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20475295-G-C

31356696-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20475427-T-A

31356749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20475481-T-C

31356749-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20475481-T-G

31357334-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20476060-A-T

31357348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20476103-T-C

31357375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20476131-G-T

31357595-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20476344-T-G

31358237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20476851-T-C

31358295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20476906-G-A

31358743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20477195-C-T

31359104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20477518-C-T

31359153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3048
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20477561-G-A