109172211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 3 prime UTR variant
orthologous variants: 56993395-A-G

109172224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 3 prime UTR variant
orthologous variants: 56993408-T-C

109172349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 3 prime UTR variant
orthologous variants: 56993530-G-T

http://identifiers.org/hco/9/GRCh38#109172362-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#56993543-C-A

109172362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 3 prime UTR variant
orthologous variants: 56993543-C-T

109172445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 3 prime UTR variant
orthologous variants: 56993625-T-C

109172446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 3 prime UTR variant
orthologous variants: 56993626-A-G

109172447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 3 prime UTR variant
orthologous variants: 56993627-G-T

109172449-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 3 prime UTR variant
orthologous variants: 56993629-G-C

http://identifiers.org/hco/9/GRCh38#109172479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#56993663-C-A

109172479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 3 prime UTR variant
orthologous variants: 56993663-C-T

109172498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 3 prime UTR variant
orthologous variants: 56993682-A-G

109172698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 3 prime UTR variant
orthologous variants: 56993880-G-A

109172745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 3 prime UTR variant
orthologous variants: 56993924-T-C

109172792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 3 prime UTR variant
orthologous variants: 56993968-T-C

109172815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 3 prime UTR variant
orthologous variants: 56993991-C-T

109172863-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 3 prime UTR variant
orthologous variants: 56994032-A-T

109173003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 3 prime UTR variant
orthologous variants: 56994172-A-G

109173220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 3 prime UTR variant
orthologous variants: 56994395-G-T

109173221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 3 prime UTR variant
orthologous variants: 56994396-G-T

109173314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 3 prime UTR variant
orthologous variants: 56994487-G-T

109173614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 3 prime UTR variant
orthologous variants: 56994799-A-G

109174032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 3 prime UTR variant
orthologous variants: 56995230-C-T

109174514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 3 prime UTR variant
orthologous variants: 56995695-G-T

109174614-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: synonymous variant
orthologous variants: 56995794-T-A

109174614-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: synonymous variant
orthologous variants: 56995794-T-G

109174742-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 56995895-A-T

109174763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 56995916-T-C

109174792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 56995949-G-A

109175332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 56996455-A-G

109175352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 56996475-T-C

109175854-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 56998734-T-G

109176017-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 56998886-T-A

109176079-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 56998944-C-G

109176144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 56999016-T-C

109176324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 56999269-A-G

109176396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 56999363-C-T

http://identifiers.org/hco/9/GRCh38#109176420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#56999469-C-A

109176420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 56999469-C-T

109176423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 56999472-T-C

109176427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 56999476-T-C

109176447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 56999507-G-T

http://identifiers.org/hco/9/GRCh38#109176478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#56999532-C-A

109176610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: synonymous variant
orthologous variants: 56999641-C-T

109176748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 56999773-C-T

109176770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 56999794-G-T

109176783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 56999807-G-T

http://identifiers.org/hco/9/GRCh38#109176814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#56999829-C-A

109176814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 56999829-C-T

http://identifiers.org/hco/9/GRCh38#109177308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57001495-C-A

109177308-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57001495-C-G

109177308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57001495-C-T

109177373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57001544-C-T

109177389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57001560-T-C

109177843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57001781-A-G

109179378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57003951-A-G

109179434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57003997-G-A

109179464-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57004030-T-A

109179567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57004126-T-C

109179817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57004721-C-T

109179965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57004873-C-T

109179973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57004881-A-G

109180171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57005042-G-A

109180241-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57005113-G-C

109180469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57005351-T-C

109180516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57005391-G-A

109180942-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57005656-G-C

109180985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57005684-G-A

109181116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57005805-A-G

109181124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57005813-G-A

109181609-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57006195-T-G

109181610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57006196-G-A

109181752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57006537-C-T

109181844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57006609-C-T

http://identifiers.org/hco/9/GRCh38#109181849-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57006614-A-C

109182076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57006766-G-A

109182076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57006766-G-T

109182573-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57007808-T-G

http://identifiers.org/hco/9/GRCh38#109182579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57007813-C-A

109182579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57007813-C-T

109182585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57007819-G-A

109182593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57007825-A-G

109182606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57007838-A-G

109182606-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57007838-A-T

109182614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57007846-G-A

109182614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57007846-G-T

109182615-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57007847-A-T

109182789-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 57007969-T-A

109182873-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57008050-T-A

109183459-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57008504-A-T

109183534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron_variant, undefined
orthologous variants: 57008562-T-C

109183610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron_variant, undefined
orthologous variants: 57008627-G-A

109184009-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57008984-T-A

109184009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57008984-T-C

109184106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57009056-C-T

109184127-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57009085-T-G

109184754-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57009379-G-C

109184768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57009393-T-C

109184821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57009443-C-T

109185045-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57009649-T-A

109185046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57009650-G-A

109185046-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57009650-G-C

109185074-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57009658-T-A

109185074-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57009658-T-G

109185090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57009678-C-T

http://identifiers.org/hco/9/GRCh38#109185250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57009819-C-A

109185353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57009927-G-A

109185353-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57009927-G-C

109185353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57009927-G-T

109185433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57010005-G-A

109185433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57010005-G-T

109185438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57010010-T-C

109185552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 57010125-G-A

109185552-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 57010125-G-C

109185628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57010203-A-G

109185713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57010280-A-G

http://identifiers.org/hco/9/GRCh38#109185832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57010402-C-A

109186891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57010847-C-T

109186932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57010892-C-T

109187034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57011015-T-C

109187329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57011309-G-A

109187329-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57011309-G-C

109187349-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57011329-C-G

109187990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57011989-C-T

109188005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57012005-A-G

109188139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57012137-A-G

109188313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57012323-A-G

109188348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57012351-C-T

http://identifiers.org/hco/9/GRCh38#109188351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57012354-C-A

109188357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57012362-G-A

109188712-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57012703-T-A

109188712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57012703-T-C

109188840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57012822-A-G

109190138-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57013078-T-G

109190251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57013199-T-C

http://identifiers.org/hco/9/GRCh38#109190358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57013288-C-A

109190467-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57013386-G-C

http://identifiers.org/hco/9/GRCh38#109190514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57013431-C-A

109190514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57013431-C-T

109190551-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57013467-C-G

109190551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57013467-C-T

109190670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57013598-A-G

109190706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57013620-T-C

109190764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57013678-T-C

109190838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57013729-T-C

109191001-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57013819-G-C

109191014-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57013835-G-C

109191028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57013860-C-T

http://identifiers.org/hco/9/GRCh38#109191139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57013958-C-A

109191139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57013958-C-T

http://identifiers.org/hco/9/GRCh38#109191413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57014161-C-A

109191413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57014161-C-T

109191476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57014222-T-C

109191724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57014414-G-T

http://identifiers.org/hco/9/GRCh38#109191751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57014445-C-A

109191751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57014445-C-T

109191966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57016556-C-T

109192126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57016718-G-A

109192126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57016718-G-T

http://identifiers.org/hco/9/GRCh38#109192127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57016719-C-A

109192127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57016719-C-T

109192129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57016721-T-C

http://identifiers.org/hco/9/GRCh38#109192208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57016786-C-A

109192208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57016786-C-T

109192209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57016787-A-G

109192210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57016788-T-C

109192334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: missense variant
orthologous variants: 57016910-C-T

109192386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57016963-A-G

109192430-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57017005-A-T

109192441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57017016-G-A

109192441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57017016-G-T

http://identifiers.org/hco/9/GRCh38#109192479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57017068-C-A

109192479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57017068-C-T

109192514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57017103-G-A

109193064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57017509-C-T

109193344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57018311-T-C

109193445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57018406-G-A

109193469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57018429-A-G

109193554-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57018523-T-G

109194195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57019751-G-A

109194195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57019751-G-T

109194480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57020042-T-C

109194505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57020063-G-A

109194505-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57020063-G-C

109194505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57020063-G-T

109194618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57020262-T-C

109194836-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57020556-T-A

109197846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57022058-G-A

109197931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57022130-A-G

109197931-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57022130-A-T

109198169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57022380-T-C

109198217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57022428-T-C

109199716-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57023928-G-C

109199732-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57023932-T-G

109199897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57024064-C-T

http://identifiers.org/hco/9/GRCh38#109200154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57024273-C-A

109200154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57024273-C-T

109200155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57024274-A-G

109200155-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57024274-A-T

109200218-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57024315-T-A

109200218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57024315-T-C

http://identifiers.org/hco/9/GRCh38#109200274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57024376-C-A

109200297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: missense variant
orthologous variants: 57024399-C-T

109200316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: synonymous variant
orthologous variants: 57024418-A-G

109200412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57024490-T-C

109200773-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57024838-T-A

109201062-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57025903-C-G

109201847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57026271-C-T

109202141-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57026545-G-C

109202282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57026724-A-G

109202351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57026803-A-G

109202433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57026875-A-G

109203192-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57027206-C-G

109203282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57027262-G-A

109203296-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57027276-T-G

109203324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57027302-G-A

109203324-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57027302-G-C

109203536-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57027452-G-C

109203536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57027452-G-T

http://identifiers.org/hco/9/GRCh38#109203539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57027455-C-A

109203539-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57027455-C-G

109203539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57027455-C-T

109203561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57027479-T-C

109203591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57027525-G-A

109203591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57027525-G-T

109203600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57027534-T-C

109203603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57027537-A-G

109203608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57027542-T-C

109203755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57027697-G-A

109203755-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57027697-G-C

109203755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57027697-G-T

109203938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57027895-C-T

109204100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57028056-C-T

109204171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57028120-G-A

109204518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57028393-G-T

109205533-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57029069-T-G

109206154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57030683-A-G

109206520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57030877-G-A

109207100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57031418-C-T

http://identifiers.org/hco/9/GRCh38#109207779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57031997-C-A

109207779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57031997-C-T

http://identifiers.org/hco/9/GRCh38#109207835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57032041-C-A

109207835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57032041-C-T

109207993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: synonymous variant
orthologous variants: 57032184-A-G

http://identifiers.org/hco/9/GRCh38#109208017-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57032208-A-C

109208031-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: missense variant
orthologous variants: 57032222-A-T

109208083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57032276-A-G

109208130-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57032325-T-A

http://identifiers.org/hco/9/GRCh38#109208171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57032366-C-A

109208171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57032366-C-T

109208181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57032376-T-C

109208194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57032389-G-A

109208194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57032389-G-T

109208196-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57032392-T-A

109208196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57032392-T-C

109208196-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57032392-T-G

109208399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57032574-T-C

109208556-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57032803-T-A

http://identifiers.org/hco/9/GRCh38#109208587-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57032835-A-C

http://identifiers.org/hco/9/GRCh38#109208635-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57032883-A-C

109209056-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57033294-C-G

109209166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57033511-T-C

109209227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57033573-T-C

109209229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57033587-G-A

109209833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57034487-C-T

109209853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57034507-T-C

109210007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57034653-G-A

109210569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57035203-C-T

http://identifiers.org/hco/9/GRCh38#109210669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57035308-C-A

109210669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57035308-C-T

109210921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57036062-G-T

109210970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57036106-T-C

109211136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57036261-C-T

http://identifiers.org/hco/9/GRCh38#109211148-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57036273-A-C

109213775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: synonymous variant
orthologous variants: 57038578-G-A

109213816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 57038619-G-A

http://identifiers.org/hco/9/GRCh38#109213889-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57038692-C-A

109213889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57038692-C-T

109213934-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57038729-T-A

http://identifiers.org/hco/9/GRCh38#109213936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57038731-C-A

109213991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57038759-G-A

109214193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57038968-G-A

109214594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57039376-G-A

109214694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57039471-G-A

109214788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57039557-C-T

http://identifiers.org/hco/9/GRCh38#109216911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57040816-C-A

109216911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57040816-C-T

109216986-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: synonymous variant
orthologous variants: 57040905-T-A

109217325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57041195-G-A

109219717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57042052-T-C

109219853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57042187-T-C

109219931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57042262-G-T

109220056-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57042380-C-G

109220135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57042472-A-G

109220405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57042746-G-A

http://identifiers.org/hco/9/GRCh38#109221315-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57043418-A-C

109221357-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57043460-T-G

109221433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57043524-C-T

109221537-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57043629-G-C

109221613-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57043711-T-G

109221817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57043877-G-A

109221817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57043877-G-T

109221923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57043978-C-T

109221974-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57044021-T-G

109222355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57044822-C-T

109222414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57044894-C-T

109222423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57044909-T-C

109222427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57044912-G-T

109222443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57044927-G-A

109222467-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57044953-T-A

109222467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57044953-T-C

109222467-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57044953-T-G

109222486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57044972-G-A

109222576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57045075-G-A

109223511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57045182-C-T

109223620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57045298-A-G

109223620-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57045298-A-T

109224285-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57045635-C-G

http://identifiers.org/hco/9/GRCh38#109224384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57045728-C-A

109224421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57045763-C-T

109224551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57045874-G-A

109224551-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57045874-G-C

109224635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57045955-G-A

109224702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57046012-T-C

109224738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57046053-A-G

109225234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57046483-A-G

109225243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57046492-A-G

109227124-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57047363-C-G

109227124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57047363-C-T

109227292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57047548-T-C

109227314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57047565-G-A

109227487-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57047768-T-A

http://identifiers.org/hco/9/GRCh38#109227488-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57047769-A-C

109228152-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57048502-C-G

109228194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57048543-G-A

109228295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57048649-T-C

109228312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57048666-C-T

109228726-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57049096-T-A

109229153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57049480-G-T

http://identifiers.org/hco/9/GRCh38#109229595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57050052-C-A

109229595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57050052-C-T

109229596-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57050053-A-T

109229849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57050246-C-T

109230031-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57050401-T-A

109230054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57050423-C-T

109230337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57050686-A-G

109230368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57050717-T-C

109230612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57050941-T-C

109230723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57051054-G-A

109231333-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57051742-G-C

109231483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57051893-A-G

109231621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57052016-G-A

109231703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57052083-A-G

109231728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57052107-C-T

109231786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57052169-G-A

109232968-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57053512-C-G

109232976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57053524-G-A

109233353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57053865-G-A

109233855-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57054294-G-C

http://identifiers.org/hco/9/GRCh38#109234085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57054456-C-A

109234162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57054516-T-C

109234177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57054530-G-T

109234178-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57054531-T-A

109234178-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57054531-T-G

109234372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57054727-T-C

109234388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57054743-G-A

109234934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57055566-A-G

109235216-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57055855-C-G

109235216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57055855-C-T

109235223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57055862-T-C

http://identifiers.org/hco/9/GRCh38#109235254-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57055889-A-C

109235274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57055908-G-A

109235970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57057395-C-T

109236127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57057555-T-C

109236831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57058677-T-C

109237145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57058996-A-G

109237269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57059127-T-C

109237385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57059227-T-C

109237815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57059607-G-T

109237863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57059647-C-T

109237883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57059671-A-G

109237924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57059742-C-T

109237950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57059768-G-T

http://identifiers.org/hco/9/GRCh38#109238041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57059845-C-A

109238083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57059892-G-A

109238146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57059938-G-T

109238404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57060172-G-A

109238440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57060198-T-C

109238582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57060318-A-G

109238602-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57060336-G-C

109238862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57060582-G-A

109239487-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57061077-G-C

109239644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57061229-G-A

109239647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57061232-C-T

109239670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57061250-T-C

http://identifiers.org/hco/9/GRCh38#109239878-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57061400-A-C

109239894-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57061409-T-A

109239899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57061414-T-C

http://identifiers.org/hco/9/GRCh38#109239957-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57061474-A-C

http://identifiers.org/hco/9/GRCh38#109240054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57061552-C-A

109240063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57061561-A-G

109240131-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57061619-T-A

109240232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57061753-C-T

109240285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57061810-G-A

109240303-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57061828-A-T

109240325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57061850-G-A

109240325-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57061850-G-C

109240325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57061850-G-T

http://identifiers.org/hco/9/GRCh38#109240339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57061868-C-A

109240339-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57061868-C-G

109240375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57061907-T-C

109240495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57062016-C-T

http://identifiers.org/hco/9/GRCh38#109240558-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57062082-A-C

109240633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57062159-G-A

109240633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57062159-G-T

109240733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57062255-A-G

109240733-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57062255-A-T

109240734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57062256-G-A

109240734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57062256-G-T

http://identifiers.org/hco/9/GRCh38#109240797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57062320-C-A

109240960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57062450-T-C

http://identifiers.org/hco/9/GRCh38#109240971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57062461-C-A

http://identifiers.org/hco/9/GRCh38#109240994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57062484-C-A

109241024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57062513-T-C

109241199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57062664-T-C

109241221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57062684-G-A

109241221-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57062684-G-C

109241225-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57062688-T-A

109241225-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57062688-T-G

http://identifiers.org/hco/9/GRCh38#109241258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57062722-C-A

109241258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57062722-C-T

109241274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57062741-C-T

109241307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57062775-G-A

109241307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57062775-G-T

109241316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57062784-T-C

109241361-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57062839-A-T

109241474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57062950-G-T

http://identifiers.org/hco/9/GRCh38#109241579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57063030-C-A

109241579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57063030-C-T

109241591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57063038-T-C

109241671-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 57063114-A-T

109241704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron_variant, missense_variant
orthologous variants: 57063147-C-T

109241858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57063301-C-T

http://identifiers.org/hco/9/GRCh38#109241878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57063323-C-A

109241896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57063341-G-A

109241899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57063344-G-A

109241899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57063344-G-T

109241912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57063352-T-C

109241913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57063353-G-T

109241930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57063368-A-G

109242061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57063500-T-C

109242061-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57063500-T-G

109242116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57063535-C-T

109242425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57063793-A-G

109242616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57063993-G-A

109242626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57064004-T-C

109242921-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57064254-T-G

http://identifiers.org/hco/9/GRCh38#109243095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57064387-C-A

109243095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57064387-C-T

http://identifiers.org/hco/9/GRCh38#109243100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57064392-C-A

http://identifiers.org/hco/9/GRCh38#109243272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57064495-C-A

109243272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57064495-C-T

109243501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57064701-G-A

109243501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57064701-G-T

109243504-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57064704-T-G

http://identifiers.org/hco/9/GRCh38#109243737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57064918-C-A

109243737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57064918-C-T

109243763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57064949-T-C

109243922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57065123-G-T

109243923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57065124-G-A

109243923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57065124-G-T

109243985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57065176-G-A

109244283-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57065385-T-A

109244301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57065403-G-A

109244327-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57065405-T-A

109244327-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57065405-T-G

109244329-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57065407-A-T

109244731-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57065534-G-C

109244734-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57065537-C-G

109244750-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57065553-G-C

109245154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57065938-T-C

109245446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57066163-T-C

109245446-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57066163-T-G

109245652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57066325-C-T

109245794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57066446-G-A

http://identifiers.org/hco/9/GRCh38#109245847-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57066494-A-C

109245878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57066522-A-G

109245956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57066592-G-A

109246781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57067453-T-C

109246819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57067491-A-G

109247326-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57067923-G-C

http://identifiers.org/hco/9/GRCh38#109247637-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57068223-A-C

109247856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57068394-T-C

109247892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57068429-T-C

109248044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57068577-G-A

109248199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron_variant, undefined
orthologous variants: 57068689-G-A

109248199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron_variant, undefined
orthologous variants: 57068689-G-T

109248383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron_variant, undefined
orthologous variants: 57068841-G-A

109249500-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57069678-G-C

109250922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57070359-G-A

109251004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57070437-T-C

109251125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57070654-C-T

http://identifiers.org/hco/9/GRCh38#109251354-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57070928-A-C

109251354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57070928-A-G

109251354-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57070928-A-T

109251360-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57070934-G-C

109251360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57070934-G-T

http://identifiers.org/hco/9/GRCh38#109251434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57071005-C-A

109251434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57071005-C-T

http://identifiers.org/hco/9/GRCh38#109251500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57071071-C-A

109251500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: missense variant
orthologous variants: 57071071-C-T

109251510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 57071081-T-C

http://identifiers.org/hco/9/GRCh38#109251551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57071114-C-A

109251551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57071114-C-T

109251635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57071200-A-G

109251795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57071380-A-G

109252039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57071908-G-A

109252306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57072184-A-G

109252321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57072220-A-G

http://identifiers.org/hco/9/GRCh38#109252330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57072229-C-A

109252746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57072644-G-T

109252748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57072646-G-A

109252827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57072732-G-A

109252984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57072885-G-A

109253555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 57073376-G-T

109253676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57073506-G-A

109253676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57073506-G-T

109253699-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57073530-C-G

109253699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57073530-C-T

http://identifiers.org/hco/9/GRCh38#109253772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#57073600-C-A

109254058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57073898-T-C

109254186-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57074047-C-G

109254186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57074047-C-T

109254796-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57074849-T-G

109254798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57074851-T-C

109254824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57074877-A-G

109255065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57075706-G-A

109255117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57075757-T-C

109255268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57075905-C-T

http://identifiers.org/hco/9/GRCh38#109255365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57076164-C-A

109255427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57076214-C-T

109255435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57076222-T-C

109255507-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57076287-C-G

109255507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57076287-C-T

109255741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57076502-C-T

109255751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57076512-G-A

109255765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57076525-C-T

http://identifiers.org/hco/9/GRCh38#109255880-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57076641-C-A

109255880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57076641-C-T

109255887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57076648-A-G

http://identifiers.org/hco/9/GRCh38#109255907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57076665-C-A

109255910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57076668-T-C

http://identifiers.org/hco/9/GRCh38#109256311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57077082-C-A

109256311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57077082-C-T

109256383-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57077154-C-G

109256383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57077154-C-T

109256523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57077294-A-G

109256523-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57077294-A-T

http://identifiers.org/hco/9/GRCh38#109256549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57077319-C-A

109256549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57077319-C-T

109256568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57077338-G-A

109256568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57077338-G-T

http://identifiers.org/hco/9/GRCh38#109256636-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57077406-A-C

109256639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57077409-T-C

109257268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57077689-G-T

http://identifiers.org/hco/9/GRCh38#109258036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57078700-C-A

109258036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57078700-C-T

109258044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57078709-A-G

109258284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: synonymous variant
orthologous variants: 57078982-C-T

http://identifiers.org/hco/9/GRCh38#109258357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57079071-C-A

http://identifiers.org/hco/9/GRCh38#109258400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57079114-C-A

109258400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57079114-C-T

109258676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57079328-G-A

109258676-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57079328-G-C

109258716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57079368-C-T

109258746-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57079399-T-A

109258838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57079464-G-A

109259212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57079738-T-C

109259499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57080961-G-T

109259502-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57080964-A-T

109259632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57081074-T-C

109259805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57081216-C-T

109261379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57082077-T-C

109261496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57082248-G-A

109261496-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57082248-G-C

109261516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57082262-G-T

109261620-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57082342-A-T

109261820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57082552-C-T

http://identifiers.org/hco/9/GRCh38#109262125-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57082988-A-C

109262418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57083194-T-C

109262495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57083244-G-A

109262608-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57083322-T-G

109262632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57083343-C-T

109262906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57083877-G-A

109262906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57083877-G-T

http://identifiers.org/hco/9/GRCh38#109262909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57083880-C-A

109262909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57083880-C-T

109262917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57083887-G-T

http://identifiers.org/hco/9/GRCh38#109262957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57083931-C-A

109262957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57083931-C-T

109262967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57083941-G-A

109262967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57083941-G-T

109262984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57083958-A-G

http://identifiers.org/hco/9/GRCh38#109263034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57084007-C-A

109263034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57084007-C-T

109263035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57084008-T-C

http://identifiers.org/hco/9/GRCh38#109263112-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57084087-A-C

http://identifiers.org/hco/9/GRCh38#109263174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57084141-C-A

http://identifiers.org/hco/9/GRCh38#109263175-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57084142-A-C

109263175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57084142-A-G

109263175-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57084142-A-T

109263180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57084147-T-C

109263196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57084163-T-C

109263196-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57084163-T-G

109263314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57084251-A-G

109263508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57084428-C-T

http://identifiers.org/hco/9/GRCh38#109263541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57084461-C-A

109263545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57084465-G-A

109263872-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57084623-G-C

109263909-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57084661-C-G

109263910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57084662-T-C

109263911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57084663-A-G

109263945-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57084697-G-C

109264175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57084887-C-T

109264369-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57085273-G-C

109264832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57085854-T-C

109264938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57085954-T-C

109264938-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57085954-T-G

http://identifiers.org/hco/9/GRCh38#109265112-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57086131-A-C

http://identifiers.org/hco/9/GRCh38#109265113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57086132-C-A

109265113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57086132-C-T

109265143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57086161-G-A

109265143-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57086161-G-C

109265268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57086279-G-A

109265344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57086359-G-A

109265385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57086400-G-A

109265385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57086400-G-T

109266657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57087467-A-G

109266658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57087468-T-C

109266658-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57087468-T-G

109266962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57087584-T-C

http://identifiers.org/hco/9/GRCh38#109266971-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57087593-A-C

109267180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57087722-T-C

109267409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57087921-G-T

http://identifiers.org/hco/9/GRCh38#109267412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57087924-C-A

109267412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57087924-C-T

109267430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57087942-G-A

109267430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57087942-G-T

109267454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57087963-G-A

109267454-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57087963-G-C

109267454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57087963-G-T

109267465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 57087978-T-C

109267466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 57087979-G-T

109267584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57088097-T-C

109267603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57088106-A-G

http://identifiers.org/hco/9/GRCh38#109267830-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57088244-A-C

109268253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57088667-A-G

109268253-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57088667-A-T

109268487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57088884-A-G

109268488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57088885-G-A

109268488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57088885-G-T

109268497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57088893-G-A

109268497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57088893-G-T

109268519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57088915-A-G

http://identifiers.org/hco/9/GRCh38#109268537-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57088929-A-C

http://identifiers.org/hco/9/GRCh38#109268571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57088966-C-A

109268571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57088966-C-T

109268614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57089007-G-A

109268982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57090784-C-T

109269244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57091033-C-T

109269286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57091060-T-C

109269410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57091181-G-A

109269474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57091230-A-G

109269477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57091233-C-T

109269598-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57091255-C-G

109269663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57091297-C-T

109269664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57091298-C-T

109269756-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57091377-T-G

109269811-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57091433-T-G

109270061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57091688-G-A

109270066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57091692-T-C

109270298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57091918-T-C

109270332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57091959-T-C

109270498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57092356-C-T

109270537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57092396-C-T

http://identifiers.org/hco/9/GRCh38#109270877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57092732-C-A

109271017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57092871-T-C

109271202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57093040-C-T

109271436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57093245-T-C

109271436-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57093245-T-G

109271642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57093416-C-T

109271648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57093422-C-T

109271889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57093666-T-C

109271933-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57093710-G-C

http://identifiers.org/hco/9/GRCh38#109271972-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57093748-A-C

109272845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57093982-G-T

109274020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57094658-A-G

109274230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57094868-A-G

109274249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57094886-T-C

109274459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57095077-G-A

109274480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57095098-A-G

109274516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57095139-G-T

109274532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57095159-A-G

109274705-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57095303-G-C

109274838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57095439-T-C

109274840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57095441-T-C

109274883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57095477-G-T

http://identifiers.org/hco/9/GRCh38#109274967-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57095570-A-C

109274999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57095602-G-A

109275041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57095636-T-C

109275564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57096138-T-C

http://identifiers.org/hco/9/GRCh38#109275622-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57096187-A-C

109275717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57096654-C-T

http://identifiers.org/hco/9/GRCh38#109276274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57097229-C-A

109276285-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57097231-T-A

109276325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57097261-G-A

109276431-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57097366-G-C

109276480-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57097420-T-A

109276632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57097574-G-A

109277038-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57097948-C-G

109277077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57097988-T-C

109277120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57098012-C-T

109277300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57100989-T-C

109277300-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57100989-T-G

109278065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57101601-G-A

109278188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57101692-G-A

109278392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57101859-C-T

109278710-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57102433-T-A

109278778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57102516-C-T

109278781-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57102519-T-G

109279684-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57103304-A-T

http://identifiers.org/hco/9/GRCh38#109279686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57103306-C-A

109279686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57103306-C-T

109279797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57103405-G-A

109279797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57103405-G-T

http://identifiers.org/hco/9/GRCh38#109280029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57103630-C-A

109284806-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57107727-C-G

109284871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57107665-A-G

109284871-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57107665-A-T

109284941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57107596-C-T

109284993-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57107545-C-G

109285051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57107487-A-G

109285141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57107398-C-T

109285176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57107357-G-A

http://identifiers.org/hco/9/GRCh38#109285215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57107326-C-A

109285215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57107326-C-T

109286071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57108300-C-T

109286110-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57108339-G-T

109286348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57108452-G-A

109286424-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57108528-G-C

109286815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57109497-T-C

109286994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57109654-T-C

http://identifiers.org/hco/9/GRCh38#109287083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57109735-C-A

109287138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57109783-C-T

109287233-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57109884-T-A

109287332-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57109988-G-C

109287433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57110087-A-G

109287480-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron_variant, undefined
orthologous variants: 57110134-A-T

http://identifiers.org/hco/9/GRCh38#109287513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57110170-C-A

109287542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57110199-C-T

http://identifiers.org/hco/9/GRCh38#109289222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57110563-C-A

109289281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57110613-C-T

109289455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57110744-A-G

109289524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57110814-A-G

109289578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57110870-G-A

109289709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57111029-A-G

109289931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57112076-T-C

109289960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron_variant, undefined
orthologous variants: 57112105-C-T

109290079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron_variant, undefined
orthologous variants: 57112201-C-T

109290130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57112250-T-C

109290222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57112344-C-T

109290288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57112399-G-T

http://identifiers.org/hco/9/GRCh38#109290638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57112726-C-A

109291160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57114390-A-G

109291433-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57114728-G-C

109291508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57114804-T-C

109291583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57114878-G-A

109291624-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57114919-A-T

109291750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57115032-C-T

http://identifiers.org/hco/9/GRCh38#109291861-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57115115-A-C

109292002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57115258-A-G

109292011-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57115267-T-G

109292158-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57115467-C-G

109292566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57115804-T-C

109292623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57116106-C-T

109292777-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57116260-G-C

109292777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57116260-G-T

109293021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57116510-A-G

http://identifiers.org/hco/9/GRCh38#109293713-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57116879-A-C

109294820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57117655-C-T

109294945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57117773-C-T

109294996-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57117830-G-C

109295123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57117958-G-A

109295187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57118010-G-A

http://identifiers.org/hco/9/GRCh38#109295271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57118097-C-A

109295271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57118097-C-T

109295332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57118156-C-T

109295374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57118191-G-A

http://identifiers.org/hco/9/GRCh38#109295444-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57118260-A-C

http://identifiers.org/hco/9/GRCh38#109295480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57118340-C-A

http://identifiers.org/hco/9/GRCh38#109295746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57118820-C-A

109296257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57119849-G-A

109296258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57119850-C-T

109296293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57119884-C-T

109296362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57119958-G-A

109296362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57119958-G-T

109296549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57120128-G-A

109297151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57120605-C-T

109297168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57120622-A-G

109297169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57120623-T-C

109297169-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57120623-T-G

http://identifiers.org/hco/9/GRCh38#109297250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57120676-C-A

109297357-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57120775-G-C

109297646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57121021-T-C

109297871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57121215-A-G

109297905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57121248-T-C

109297955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57121289-A-G

109297991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57121325-G-A

109298007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57121341-T-C

109298170-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57122020-A-T

109298262-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57122113-T-G

109299494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57122781-G-A

109299494-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57122781-G-C

http://identifiers.org/hco/9/GRCh38#109299738-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57122830-A-C

109300157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57123216-G-T

109303990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57126673-T-C

109304023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57126710-G-A

109304166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57126850-A-G

109304580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57127270-G-A

109304898-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57127583-C-G

109304898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57127583-C-T

109304937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57127605-A-G

109305018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57127651-C-T

109305229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57127818-G-T

109305282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57127862-T-C

109305357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57127924-G-A

109307183-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57128993-T-A

109307183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57128993-T-C

109307183-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57128993-T-G

109307286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57129620-G-T

109307362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57129695-C-T

http://identifiers.org/hco/9/GRCh38#109307781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57130073-C-A

http://identifiers.org/hco/9/GRCh38#109307881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57130158-C-A

109307881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57130158-C-T

109307984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57130237-G-T

109308027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57130262-C-T

109308104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57130343-C-T

109309908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57132450-G-A

109310143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57132701-T-C

http://identifiers.org/hco/9/GRCh38#109310192-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57132750-A-C

109310257-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57132811-T-A

http://identifiers.org/hco/9/GRCh38#109310333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57132866-C-A

109310427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57132952-G-A

109310558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57133209-G-A

109310770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57133592-G-A

109310790-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57133630-T-G

109311033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57133999-G-A

109311033-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57133999-G-C

109311033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57133999-G-T

109311037-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57134003-G-C

109311193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57134133-T-C

109311386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57134297-G-T

109311506-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57134427-G-C

109311766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57134659-T-C

109312269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57135188-A-G

109312272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57135192-T-C

109312459-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57135561-G-C

109312516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57135619-C-T

109312803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57135890-T-C

109312833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57135917-G-A

109313113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57136037-C-T

109313138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57136062-C-T

http://identifiers.org/hco/9/GRCh38#109313181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57136090-C-A

http://identifiers.org/hco/9/GRCh38#109313231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57136149-C-A

109313231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57136149-C-T

109313233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57136151-C-T

http://identifiers.org/hco/9/GRCh38#109313415-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57136329-A-C

109313436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57136350-G-A

109313436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57136350-G-T

109314478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57137538-C-T

109314737-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57137757-G-C

http://identifiers.org/hco/9/GRCh38#109314968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57137956-C-A

109315060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57138052-C-T

109315377-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57138346-T-A

109315381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57138350-G-A

http://identifiers.org/hco/9/GRCh38#109315784-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57138929-A-C

109315798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57138955-T-C

109315922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57139159-T-C

109316002-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57139225-G-C

109316055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron_variant, undefined
orthologous variants: 57139289-A-G

109316221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57139436-A-G

109316678-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57139890-T-A

109317310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57140197-C-T

109317348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57140225-G-T

http://identifiers.org/hco/9/GRCh38#109317415-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57140266-A-C

109317596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57140442-G-T

109317937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57140777-C-T

109317959-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57140803-T-G

109318223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57141049-T-C

109318227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57141053-G-A

109318228-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57141054-G-C

109318296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57141118-A-G

http://identifiers.org/hco/9/GRCh38#109318302-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57141137-A-C

109318446-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57141298-C-G

109318853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57141671-T-C

109318859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57141677-T-C

109319358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57142131-C-T

http://identifiers.org/hco/9/GRCh38#109319434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57142206-C-A

109319434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57142206-C-T

109319513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57142268-G-A

109319513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57142268-G-T

109319775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57142497-G-A

109319970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57142678-G-A

http://identifiers.org/hco/9/GRCh38#109320037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57142740-C-A

109320037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57142740-C-T

http://identifiers.org/hco/9/GRCh38#109320092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57142799-C-A

109320092-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57142799-C-G

109320092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57142799-C-T

109320094-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57142801-T-A

109320094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57142801-T-C

109320099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57142806-G-A

109320099-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57142806-G-C

109320099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57142806-G-T

http://identifiers.org/hco/9/GRCh38#109320128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#57142835-C-A

109320128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: intron variant
orthologous variants: 57142835-C-T

109320431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: missense variant
orthologous variants: 57143138-G-A

109320431-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: missense variant
orthologous variants: 57143138-G-C

109320431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: missense variant
orthologous variants: 57143138-G-T

109320629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 57143322-G-T

109320793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 5 prime UTR variant
orthologous variants: 57143488-G-A

109320793-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 5 prime UTR variant
orthologous variants: 57143488-G-C

109320793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 5 prime UTR variant
orthologous variants: 57143488-G-T

109320823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 5 prime UTR variant
orthologous variants: 57143511-G-A

109320823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19818
most severe consequence: 5 prime UTR variant
orthologous variants: 57143511-G-T