89524847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 105563633-T-C

http://identifiers.org/hco/1/GRCh38#89524987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#105563745-C-A

89524987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 105563745-C-T

89525090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, undefined
orthologous variants: 105563804-G-A

89525090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, undefined
orthologous variants: 105563804-G-T

89525365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, undefined
orthologous variants: 105564074-C-T

89525438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, undefined
orthologous variants: 105564142-G-A

89525441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, undefined
orthologous variants: 105564145-G-A

89526693-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105565084-G-C

89526694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105565085-A-G

89526838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105565223-A-G

89527002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105565376-A-G

89527005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105565379-G-A

89527047-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105565419-T-G

89527079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105565454-T-C

89527165-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105565520-T-A

89527219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105565571-A-G

89527394-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105565731-C-G

89527729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105566225-C-T

89527766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105566263-T-C

89528155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105566623-G-A

89528233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105566682-C-T

89529574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105574831-C-T

http://identifiers.org/hco/1/GRCh38#89529803-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#105575101-A-C

89529826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105575134-A-G

89529915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105575222-A-G

89530693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105576199-T-C

89530856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105576332-G-A

89531014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105576459-A-G

89531118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105576567-G-T

http://identifiers.org/hco/1/GRCh38#89531291-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#105576769-A-C

89531856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105577195-T-C

89531856-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105577195-T-G

89531858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105577197-G-A

89532916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105577838-C-T

89533040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105577953-C-T

89533062-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105577976-A-T

89533634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105578478-A-G

89533686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105578530-A-G

89533751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105578595-G-A

89534048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105579210-A-G

89534062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105579223-T-C

89534063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105579224-T-C

89534063-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105579224-T-G

http://identifiers.org/hco/1/GRCh38#89534356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#105579475-C-A

89534356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105579475-C-T

89534493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105579582-A-G

89534493-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105579582-A-T

89534809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105580109-G-A

89534976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105580274-C-T

89535004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105580299-C-T

89535046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105580328-T-C

89535178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105580505-A-G

89535200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105580521-A-G

http://identifiers.org/hco/1/GRCh38#89535218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#105580540-C-A

89535760-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105581048-C-G

89535938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105581315-A-G

89536254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105581787-A-G

89536618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105582175-T-C

89536834-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105582506-T-G

89536942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105582607-A-G

http://identifiers.org/hco/1/GRCh38#89538204-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#105583144-A-C

89538260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105583202-G-A

http://identifiers.org/hco/1/GRCh38#89538301-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#105583260-A-C

89539713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105584481-G-A

89539713-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105584481-G-C

89539904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105584772-C-T

89539912-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105584780-G-C

89540144-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105585042-T-G

http://identifiers.org/hco/1/GRCh38#89540303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#105585415-C-A

89540303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105585415-C-T

89540442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105585525-G-A

89540507-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105585566-T-A

89540750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105585838-G-A

89540943-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105586437-T-G

89540963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105586465-G-A

89540969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105586473-A-G

89541148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105586584-T-C

89541364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105586779-T-C

89541587-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105586998-T-A

89542400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105587731-A-G

89542616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105587923-T-C

89542887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105588113-G-A

89542898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105588124-T-C

89542972-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105588199-T-G

89544165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105588997-G-A

89544328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105589146-C-T

89544818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105589699-T-C

89544858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105589738-A-G

89545153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105590015-A-G

89545418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105590284-C-T

89545515-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105590364-C-G

89545515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105590364-C-T

89545977-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105590716-G-C

89546306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, undefined
orthologous variants: 105591086-T-C

http://identifiers.org/hco/1/GRCh38#89546328-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#105591104-A-C

89546768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, undefined
orthologous variants: 105591490-C-T

89546834-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, undefined
orthologous variants: 105591542-T-A

89546834-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, undefined
orthologous variants: 105591542-T-G

89547172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, undefined
orthologous variants: 105592164-A-G

89547192-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, undefined
orthologous variants: 105592185-G-C

89547251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, undefined
orthologous variants: 105592260-G-T

89547393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, undefined
orthologous variants: 105592386-A-G

89547810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, undefined
orthologous variants: 105592775-A-G

89547810-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, undefined
orthologous variants: 105592775-A-T

89548096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, undefined
orthologous variants: 105593039-T-C

89548169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, undefined
orthologous variants: 105593107-A-G

89548184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, undefined
orthologous variants: 105593122-T-C

http://identifiers.org/hco/1/GRCh38#89548192-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#105593133-A-C

89548361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, undefined
orthologous variants: 105593301-A-G

89548610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, undefined
orthologous variants: 105593531-T-C

89548692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, undefined
orthologous variants: 105593589-G-T

89549067-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, undefined
orthologous variants: 105593892-G-C

89549073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, undefined
orthologous variants: 105593898-G-A

89549142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, undefined
orthologous variants: 105593948-A-G

89549747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, undefined
orthologous variants: 105597338-G-T

89549842-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, undefined
orthologous variants: 105597424-T-A

89549859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, undefined
orthologous variants: 105597439-C-T

89550119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, undefined
orthologous variants: 105597742-A-G

89550142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, undefined
orthologous variants: 105597763-A-G

89550186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, undefined
orthologous variants: 105597807-A-G

89550927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105598620-A-G

89551696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105599772-G-A

89551696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105599772-G-T

89551866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105600256-G-A

89551956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105600369-C-T

89552385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105601676-A-G

89552765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105601987-G-A

89552784-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105602006-C-G

89552927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105602147-T-C

89553092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105602309-G-T

89553505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105603320-A-G

89553805-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105603592-C-G

89553835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105603649-A-G

89553974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105603763-C-T

89554102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105603844-G-T

89554399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105604106-C-T

89554400-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105604107-A-T

89554622-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105604291-C-G

89555609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105604990-T-C

89555825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105605200-G-A

89557233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105606912-C-T

89557685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105607261-C-T

89557911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105607388-C-T

http://identifiers.org/hco/1/GRCh38#89558240-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#105607682-A-C

89562919-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105609680-G-C

89563553-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105609026-G-C

89563563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105609043-G-A

89563743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105609220-G-A

89564457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105609879-T-C

89564523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105609945-A-G

89564846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105612852-G-A

http://identifiers.org/hco/1/GRCh38#89565049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#105613064-C-A

89565197-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105613235-C-G

89565358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105613389-A-G

89565395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105613427-C-T

89565718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105613714-A-G

89565844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105613835-A-G

89566219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105614287-A-G

89566359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105614429-T-C

89566559-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105614742-T-G

89566613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105614837-A-G

89566686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105614914-A-G

89566900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105615109-A-G

89566925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105615137-A-G

http://identifiers.org/hco/1/GRCh38#89567095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#105615286-C-A

89567095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105615286-C-T

89567097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105615288-G-A

89567097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105615288-G-T

http://identifiers.org/hco/1/GRCh38#89567136-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#105615326-A-C

89567136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105615326-A-G

89567437-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105615613-C-G

89567437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105615613-C-T

89567455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105615631-A-G

89567569-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105615742-T-G

89568541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105616765-A-G

89572619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 105617993-G-A

89572619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 105617993-G-T

89572687-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105618084-G-T

http://identifiers.org/hco/1/GRCh38#89572712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#105618113-C-A

89572887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105618439-T-C

89572889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105618441-C-T

89573027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105618562-A-G

89573119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105618654-T-C

89573633-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105618886-C-G

http://identifiers.org/hco/1/GRCh38#89573973-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#105619088-A-C

89574083-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105619193-T-A

89574083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105619193-T-C

89574270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105619367-A-G

89574346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105619469-A-G

http://identifiers.org/hco/1/GRCh38#89574386-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#105619527-A-C

89574727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105619845-C-T

http://identifiers.org/hco/1/GRCh38#89574768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#105619977-C-A

89574768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105619977-C-T

89574807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105620086-T-C

89574848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105620127-G-A

89574862-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105620141-C-G

89574898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105620168-C-T

89575536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105620948-A-G

89575643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105621069-T-C

89575704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105621116-T-C

http://identifiers.org/hco/1/GRCh38#89577282-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#105621591-A-C

89577514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105621825-G-A

http://identifiers.org/hco/1/GRCh38#89577518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#105621832-C-A

89577557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105621871-T-C

89578230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105622462-A-G

89578843-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105623454-T-A

89578876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105623487-A-G

89578945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105623553-T-C

89579095-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105623702-T-G

89579174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105623778-G-A

89579216-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105623809-T-G

89579305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105623895-G-T

89579310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105623900-G-A

89579778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105624238-A-G

89579865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105624314-A-G

89580364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105625344-C-T

http://identifiers.org/hco/1/GRCh38#89580447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#105625414-C-A

89580656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron variant
orthologous variants: 105625602-A-G

89581879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, undefined
orthologous variants: 105626967-T-C

89582021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, undefined
orthologous variants: 105627108-G-A

http://identifiers.org/hco/1/GRCh38#89582486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#105627356-C-A

89582486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, undefined
orthologous variants: 105627356-C-T

http://identifiers.org/hco/1/GRCh38#89582518-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#105627382-A-C

89582518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, undefined
orthologous variants: 105627382-A-G

http://identifiers.org/hco/1/GRCh38#89582547-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#105627412-A-C

89582551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, undefined
orthologous variants: 105627417-G-A

89582551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, undefined
orthologous variants: 105627417-G-T

89582553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, undefined
orthologous variants: 105627419-G-A

89582553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, undefined
orthologous variants: 105627419-G-T

89582566-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, undefined
orthologous variants: 105627495-A-T

89582597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, undefined
orthologous variants: 105627606-T-C

89582716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: synonymous_variant, undefined
orthologous variants: 105627721-A-G

89582965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: synonymous_variant, undefined
orthologous variants: 105627970-T-C

89583002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: missense_variant, undefined
orthologous variants: 105628007-G-A

89583002-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: missense_variant, undefined
orthologous variants: 105628007-G-C

89583038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: missense_variant, undefined
orthologous variants: 105628043-C-T

89583124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: synonymous_variant, undefined
orthologous variants: 105628129-G-A

89583247-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: synonymous_variant, undefined
orthologous variants: 105628252-A-T

89583373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: synonymous_variant, undefined
orthologous variants: 105628378-G-A

89583817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 105628822-A-G

89583856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 105628861-T-C

89584018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 105629023-C-T

89584090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 105629095-T-C

89584542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 105629547-A-G

89584547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, stop_gained, undefined
orthologous variants: 105629552-C-T

89584612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 105629617-A-G

89584654-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 105629659-T-A

89584802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, undefined
orthologous variants: 105629807-A-G

89584802-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, undefined
orthologous variants: 105629807-A-T

89584846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, undefined
orthologous variants: 105629860-A-G

89584865-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, undefined
orthologous variants: 105629882-T-G

http://identifiers.org/hco/1/GRCh38#89584873-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#105629886-A-C

89584873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, undefined
orthologous variants: 105629886-A-G

89584875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, undefined
orthologous variants: 105629888-A-G

89584886-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, undefined
orthologous variants: 105629900-T-A

http://identifiers.org/hco/1/GRCh38#89584891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#105629905-C-A

89584931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, undefined
orthologous variants: 105629949-A-G

89584931-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, undefined
orthologous variants: 105629949-A-T

89586663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, undefined
orthologous variants: 105630450-A-G

89590630-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, undefined
orthologous variants: 105631811-G-C

89590789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, undefined
orthologous variants: 105631954-G-A

http://identifiers.org/hco/1/GRCh38#89590909-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#105632049-A-C

89591008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, undefined
orthologous variants: 105632123-C-T

89591566-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, undefined
orthologous variants: 105632604-A-T

89591862-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, undefined
orthologous variants: 105632844-C-G

89592070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, undefined
orthologous variants: 105632995-A-G

89592105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, undefined
orthologous variants: 105633031-G-A

89592145-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, undefined
orthologous variants: 105633071-T-A

89592214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, undefined
orthologous variants: 105633149-G-A

89592447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, undefined
orthologous variants: 105633408-G-T

89592706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, undefined
orthologous variants: 105633610-G-A

89592706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: intron_variant, undefined
orthologous variants: 105633610-G-T

89592840-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: 105633738-T-G

89592932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: 3_prime_UTR_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 105633830-A-G

89592986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: 3_prime_UTR_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 105633884-C-T

89593419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 105633999-A-G

89593419-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 105633999-A-T

89593454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 105634033-G-T

89593515-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 105634087-T-G

89593621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 105634182-A-G

89593657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 105634219-T-C

http://identifiers.org/hco/1/GRCh38#89593751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#105634302-C-A

http://identifiers.org/hco/1/GRCh38#89593833-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#105634380-A-C

89593840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 105634387-G-T

89593955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 105634487-T-C

89593960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 105634492-G-A

89593994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 105634526-T-C

89594007-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 105634540-A-T

http://identifiers.org/hco/1/GRCh38#89594150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#105634675-C-A

89594404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 105634935-C-T

89594407-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 105634938-G-T

89594409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 105634941-A-G

89594461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 105634992-G-A

89594461-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 105634992-G-C

89594461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 105634992-G-T

89594704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 105635180-G-T

http://identifiers.org/hco/1/GRCh38#89594812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#105635295-C-A

http://identifiers.org/hco/1/GRCh38#89595088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#105635526-C-A

89595311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 105635713-T-C

89595312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 105635714-G-T

89595335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 105635737-A-G

http://identifiers.org/hco/1/GRCh38#89595344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#105635746-C-A

http://identifiers.org/hco/1/GRCh38#89595383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#105635790-C-A

89595430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 105635843-A-G

http://identifiers.org/hco/1/GRCh38#89595450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#105635866-C-A

http://identifiers.org/hco/1/GRCh38#89595469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#105635891-C-A

89595641-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 105636039-C-G

89595773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 105636167-A-G

89595977-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 105636316-T-G

89596131-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 105636463-G-C

89596184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 105636491-T-C

89596373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 105636649-A-G

89596386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 105636662-A-G

89596407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 105636683-T-C

89596435-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 105636711-G-C

89596647-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 105636900-T-A

89596692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 105636932-C-T

89596721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 105636960-A-G

89596762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 105636996-A-G

89597012-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 105637145-T-A

89597190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 105637299-A-G

http://identifiers.org/hco/1/GRCh38#89597400-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#105637524-A-C

89597400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 105637524-A-G

http://identifiers.org/hco/1/GRCh38#89597424-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#105637548-A-C

http://identifiers.org/hco/1/GRCh38#89597528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#105637653-C-A

89597537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 105637662-C-T

89597567-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 105637692-T-A

89597665-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30692
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 105637784-T-A