http://identifiers.org/hco/5/GRCh38#172641363-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#26633915-C-A

172641363-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 26633915-C-G

172641363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 26633915-C-T

172641473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26634004-G-A

172641473-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26634004-G-C

172641473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26634004-G-T

172641653-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26634109-G-C

172641720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26634142-G-A

172641904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26634278-C-T

172642084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26634466-G-A

172642272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26634614-T-C

172643278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26635530-G-A

172643628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26635817-C-T

172643748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26635936-C-T

172644000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26636206-C-T

http://identifiers.org/hco/5/GRCh38#172644595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#26636802-C-A

172644870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26637074-A-G

172645062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26637220-A-G

172645069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26637227-G-A

172645268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26637392-C-T

172645527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26637701-C-T

172645528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26637702-G-A

172646720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26639478-C-T

172646852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26639580-G-A

172646852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26639580-G-T

172646899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26639621-T-C

172646899-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26639621-T-G

172647454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26639885-G-T

172647468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26639899-G-A

172647468-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26639899-G-C

172647677-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26640039-C-G

172647864-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26640142-G-C

http://identifiers.org/hco/5/GRCh38#172647877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#26640152-C-A

172647900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26640164-A-G

172648315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26640464-T-C

172648342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26640486-G-T

172648457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26640582-G-A

172648463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26640588-G-A

172648637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26640733-G-A

172648805-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26640826-C-G

172648805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26640826-C-T

172649725-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, undefined
orthologous variants: 26641309-A-T

172649904-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26641438-C-G

172649914-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26641442-A-T

172649979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26641508-T-C

172650348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26641866-T-C

172650457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26642149-A-G

172650584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26642274-G-A

172658923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26643081-T-C

172659023-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26643180-C-G

172659023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26643180-C-T

172659543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26643645-C-T

172659660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26643760-C-T

172659772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26643843-C-T

172659808-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26643879-G-C

172659812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26643883-T-C

172659995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, undefined
orthologous variants: 26643999-G-A

172660112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26644143-C-T

172660295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, undefined
orthologous variants: 26644280-G-T

172661497-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26645078-C-G

172661594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26645168-C-T

172661715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26645246-A-G

http://identifiers.org/hco/5/GRCh38#172662147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#26645689-C-A

172662147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26645689-C-T

172662224-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, undefined
orthologous variants: 26645765-C-G

172662224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, undefined
orthologous variants: 26645765-C-T

http://identifiers.org/hco/5/GRCh38#172662296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#26645827-C-A

172662296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26645827-C-T

http://identifiers.org/hco/5/GRCh38#172662353-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#26645864-C-A

172662359-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26645870-C-G

172662360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26645871-T-C

172662542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26645971-T-C

172662581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, undefined
orthologous variants: 26646011-G-A

172662684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26646111-A-G

172662758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26646161-G-A

172664376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26646835-C-T

172664459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26646904-A-G

http://identifiers.org/hco/5/GRCh38#172664613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#26647007-C-A

172664613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26647007-C-T

172664811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26647179-A-G

172664824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26647210-T-C

172664828-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26647214-G-T

http://identifiers.org/hco/5/GRCh38#172664833-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#26647219-A-C

http://identifiers.org/hco/5/GRCh38#172665097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#26647485-C-A

172665097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26647485-C-T

172665259-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26647640-G-C

172665512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26647785-A-G

172665599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26647886-C-T

172665610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26647897-G-T

http://identifiers.org/hco/5/GRCh38#172665658-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#26647939-A-C

172665663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26647944-C-T

http://identifiers.org/hco/5/GRCh38#172665668-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#26647949-A-C

172665668-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26647949-A-T

172665676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26647957-C-T

172665694-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26647978-C-G

172665694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26647978-C-T

http://identifiers.org/hco/5/GRCh38#172665698-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#26647982-A-C

172665698-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26647982-A-T

172667491-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26648902-A-T

172667536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26648958-T-C

172667702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26649089-C-T

172667715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26649102-G-A

172667782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26649165-C-T

http://identifiers.org/hco/5/GRCh38#172667830-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#26649201-A-C

http://identifiers.org/hco/5/GRCh38#172667842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#26649213-C-A

172667842-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26649213-C-G

172667842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26649213-C-T

172667880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26649255-G-A

172668326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26649619-T-C

http://identifiers.org/hco/5/GRCh38#172668454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#26649702-C-A

172668583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26649803-C-T

172668728-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26649899-A-T

172668801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26649936-G-A

172669103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26650150-C-T

172669212-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26650263-C-G

172669368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26650402-T-C

172669424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26650439-G-A

172669633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26650617-C-T

172669693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26650687-A-G

172669733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26650715-G-A

172669733-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26650715-G-C

172669733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26650715-G-T

http://identifiers.org/hco/5/GRCh38#172669755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#26650728-C-A

172669755-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26650728-C-G

172669755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26650728-C-T

172669774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26650750-T-C

http://identifiers.org/hco/5/GRCh38#172669796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#26650772-C-A

172669796-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, missense_variant
orthologous variants: 26650772-C-G

172669796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, missense_variant
orthologous variants: 26650772-C-T

http://identifiers.org/hco/5/GRCh38#172669873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#26650849-C-A

172669873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 26650849-C-T

172669882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 26650858-G-A

172669882-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 26650858-G-C

172669882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 26650858-G-T

172670026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 26651002-T-C

172670041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 26651017-G-A

172670041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 26651017-G-T

172670062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 26651038-G-A

172670062-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 26651038-G-C

172670062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 26651038-G-T

172670101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 26651077-G-A

172670101-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, missense_variant
orthologous variants: 26651077-G-T

172670125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 26651101-G-A

172670125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 26651101-G-T

http://identifiers.org/hco/5/GRCh38#172670126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#26651102-C-A

172670126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, missense_variant
orthologous variants: 26651102-C-T

http://identifiers.org/hco/5/GRCh38#172670149-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#26651125-A-C

172670149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 26651125-A-G

http://identifiers.org/hco/5/GRCh38#172670183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#26651159-C-A

172670183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 26651159-C-T

172670263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 26651239-G-A

172670263-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 26651239-G-T

http://identifiers.org/hco/5/GRCh38#172670462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#26651392-C-A

172670462-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26651392-C-G

172670462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26651392-C-T

172670501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26651423-G-A

http://identifiers.org/hco/5/GRCh38#172671270-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#26651796-A-C

172671413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26651928-C-T

172671421-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26651936-T-A

172671421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26651936-T-C

172671421-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26651936-T-G

172671702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26652106-C-T

172671841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26652200-G-A

172671953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26652313-G-T

172671985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26652344-T-C

172672022-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26652379-G-T

172672075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26652437-G-T

http://identifiers.org/hco/5/GRCh38#172672456-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#26652781-A-C

172672491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26652818-G-A

172672500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26652827-G-T

172672581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26652903-G-T

172672933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26653413-A-G

172673094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26653543-G-A

172678257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26656046-A-G

172683398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26657620-T-C

172683570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 26657792-G-A

172683570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 26657792-G-T

http://identifiers.org/hco/5/GRCh38#172683640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#26657835-C-A

172683640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, missense_variant
orthologous variants: 26657835-C-T

172683657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 26657852-G-A

172683657-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 26657852-G-C

172683657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 26657852-G-T

172683669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 26657864-G-A

172683669-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 26657864-G-C

172683669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 26657864-G-T

http://identifiers.org/hco/5/GRCh38#172683697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#26657892-C-A

172683697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, missense_variant
orthologous variants: 26657892-C-T

172683702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 26657897-G-A

172683702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 26657897-G-T

172683711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 26657906-G-A

172683711-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 26657906-G-C

172683711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 26657906-G-T

http://identifiers.org/hco/5/GRCh38#172683715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#26657910-C-A

172683715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 26657910-C-T

172683720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 26657915-G-A

172683720-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 26657915-G-C

172683720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 26657915-G-T

http://identifiers.org/hco/5/GRCh38#172683723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#26657918-C-A

172683723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 26657918-C-T

172683731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, missense_variant
orthologous variants: 26657926-A-G

172683731-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, missense_variant
orthologous variants: 26657926-A-T

172683732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 26657927-A-G

172683733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, missense_variant
orthologous variants: 26657928-G-A

172683733-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, missense_variant
orthologous variants: 26657928-G-C

172683733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, missense_variant
orthologous variants: 26657928-G-T

172683735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 26657930-G-A

172683735-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 26657930-G-C

172683735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 26657930-G-T

172683744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 26657939-A-G

172683747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 26657942-G-A

172683747-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 26657942-G-C

172683747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 26657942-G-T

172683750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 26657945-G-A

172683750-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 26657945-G-C

172683750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 26657945-G-T

http://identifiers.org/hco/5/GRCh38#172683801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#26657996-C-A

172683801-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 26657996-C-G

172683801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 26657996-C-T

172683852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 26658047-G-A

172683852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 26658047-G-T

http://identifiers.org/hco/5/GRCh38#172683930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#26658125-C-A

172683930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 26658125-C-T

172683957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 26658152-G-A

172683957-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 26658152-G-C

172683957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 26658152-G-T

172683959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, missense_variant
orthologous variants: 26658154-G-A

172683959-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, missense_variant
orthologous variants: 26658154-G-T

172684629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26658760-G-A

172684906-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26658994-A-T

http://identifiers.org/hco/5/GRCh38#172685043-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#26659081-A-C

172685336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26659295-G-A

172685410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26659378-C-T

172685490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26659451-A-G

172685871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26659764-T-C

172685873-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26659766-G-C

172685948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26659804-C-T

http://identifiers.org/hco/5/GRCh38#172686085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#26659940-C-A

172686085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron variant
orthologous variants: 26659940-C-T

172686165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 26660046-C-T

http://identifiers.org/hco/5/GRCh38#172686205-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#26660086-A-C

172686205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: synonymous variant
orthologous variants: 26660086-A-G

http://identifiers.org/hco/5/GRCh38#172686314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#26660195-C-A

172686314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, undefined
orthologous variants: 26660195-C-T

172686322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, undefined
orthologous variants: 26660202-G-A

172686322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, undefined
orthologous variants: 26660202-G-T

172686326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, undefined
orthologous variants: 26660205-G-A

172686326-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, undefined
orthologous variants: 26660205-G-C

http://identifiers.org/hco/5/GRCh38#172686383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#26660267-C-A

172686383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, undefined
orthologous variants: 26660267-C-T

172686392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, undefined
orthologous variants: 26660276-C-T

http://identifiers.org/hco/5/GRCh38#172686594-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#26660456-A-C

http://identifiers.org/hco/5/GRCh38#172686601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#26660463-C-A

172686645-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, undefined
orthologous variants: 26660491-C-G

172686645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, undefined
orthologous variants: 26660491-C-T

172686647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, undefined
orthologous variants: 26660493-T-C

172686647-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, undefined
orthologous variants: 26660493-T-G

172686736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 26660580-G-A

http://identifiers.org/hco/5/GRCh38#172686832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#26660676-C-A

172686832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 26660676-C-T

172686940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 26660778-G-A

172686940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 26660778-G-T

http://identifiers.org/hco/5/GRCh38#172687100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#26660956-C-A

172687198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 26661052-G-A

172687272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 26661124-G-A

172687272-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 26661124-G-C

172687272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 26661124-G-T

172687284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 26661138-A-G

http://identifiers.org/hco/5/GRCh38#172687289-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#26661143-A-C

172687289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 26661143-A-G

172687289-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 26661143-A-T

172687388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 26661238-G-A

172687388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 26661238-G-T

172687461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 26661316-A-G

172687492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 26661333-G-A

172687492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 26661333-G-T

172687568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 26661412-G-T

172687572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 26661426-G-T

172687695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 26661545-A-G

http://identifiers.org/hco/5/GRCh38#172687746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#26661592-C-A

http://identifiers.org/hco/5/GRCh38#172687787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#26661620-C-A

172687925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 26661679-A-G

172687992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 26661722-G-T

172688047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 26661773-C-T

172688182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 26661894-G-A

172688182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 26661894-G-T

172688189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 26661898-G-A

172688189-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 26661898-G-T

http://identifiers.org/hco/5/GRCh38#172688224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#26661944-C-A

172688224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 26661944-C-T

http://identifiers.org/hco/5/GRCh38#172688263-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#26661982-C-A

172688332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 26662040-A-G

http://identifiers.org/hco/5/GRCh38#172688337-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#26662045-C-A

172688337-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 26662045-C-G

172688506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 26662242-A-G

172688604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 26662316-A-G

172688632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 26662341-A-G

172688677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 26662378-T-C

http://identifiers.org/hco/5/GRCh38#172688728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#26662674-C-A

172688737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 26662683-T-C

172688886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 26662815-G-T

172688960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 26662892-G-T

172688981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 26662917-C-T

http://identifiers.org/hco/5/GRCh38#172689083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#26663020-C-A

172689392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 26663311-G-T

http://identifiers.org/hco/5/GRCh38#172689473-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#26663456-C-A

http://identifiers.org/hco/5/GRCh38#172689638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#26663605-C-A

172689800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 26663750-A-G

172690003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 26663863-C-T

http://identifiers.org/hco/5/GRCh38#172690112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#26663934-C-A

172690112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 26663934-C-T

172690282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 26664078-C-T

172690350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 26664148-G-T

172690436-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 26664289-C-G

172690484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 26664341-A-G

172690516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 26664376-G-T

172690544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 26664404-G-A

172690607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 26664463-G-A

172690607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 26664463-G-T

172690663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 26664512-G-A

172690663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 26664512-G-T

172690673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 26664522-G-A

172690673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 26664522-G-T

172690856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 26664639-A-G

http://identifiers.org/hco/5/GRCh38#172690898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#26664672-C-A

172690898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 26664672-C-T

172690948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 26664739-A-G

172691014-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 26664795-T-G

172691085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 26664866-T-C

http://identifiers.org/hco/5/GRCh38#172691155-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#26664963-A-C

172691155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 26664963-A-G

172691190-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 26664993-G-C

172691190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 26664993-G-T

172691214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 26665018-T-C

172691311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 26665102-T-C

172691447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35422
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 26665227-T-C