40692440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: 5 prime UTR variant
orthologous variants: 91949059-G-A

40692440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: 5 prime UTR variant
orthologous variants: 91949059-G-T

40692478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: 5 prime UTR variant
orthologous variants: 91949097-G-T

40692636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91949243-T-C

40692636-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91949243-T-G

40692722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91949317-G-A

40692722-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91949317-G-C

40692722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91949317-G-T

40692972-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, undefined
orthologous variants: 91949550-G-C

40693106-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91949682-C-G

40693106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91949682-C-T

http://identifiers.org/hco/12/GRCh38#40693236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#91949792-C-A

40693299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, undefined
orthologous variants: 91949843-C-T

40693320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91949865-G-A

40693810-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91950295-T-A

40693996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91950438-G-A

40694048-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91950489-C-G

40694259-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91950727-T-A

40694302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91950766-T-C

40694522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91950935-A-G

40694524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91950937-A-G

40694909-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91951259-A-T

40694912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91951262-G-A

40694912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91951262-G-T

40695081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91951407-A-G

40695139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91951470-C-T

40695637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91952932-A-G

40696001-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91953219-T-A

40696051-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91953268-G-C

40696368-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91953555-T-G

40696543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91953714-T-C

http://identifiers.org/hco/12/GRCh38#40696709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#91953847-C-A

40696786-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91953940-A-T

40696990-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91954496-T-G

40697135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91954637-G-A

40697529-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91955191-C-G

40697529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91955191-C-T

40697645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91955320-T-C

40697650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91955321-C-T

40697680-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91955338-T-A

40697680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91955338-T-C

40698687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91956357-C-T

40698772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91956449-C-T

40698895-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91956569-T-G

40698905-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91956580-T-A

40698905-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91956580-T-G

40698959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91956620-T-C

40698986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91956647-G-T

40699197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91956874-C-T

40699483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91957154-T-C

40699562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91957233-T-C

40700659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91958147-T-C

40700686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91958179-G-T

40700820-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91958306-A-T

40700846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91958335-T-C

40700890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91958372-C-T

http://identifiers.org/hco/12/GRCh38#40700896-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#91958378-A-C

40700992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91958470-G-T

40701719-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91959317-T-A

40704588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91970418-T-C

40704606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91970436-C-T

40705088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91970945-G-A

40705438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91971257-G-A

http://identifiers.org/hco/12/GRCh38#40706444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#91971484-C-A

40706444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91971484-C-T

http://identifiers.org/hco/12/GRCh38#40706656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#91971674-C-A

40706656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91971674-C-T

40713678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91972102-A-G

http://identifiers.org/hco/12/GRCh38#40713747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#91972157-C-A

40714054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91972585-A-G

http://identifiers.org/hco/12/GRCh38#40714065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#91972596-C-A

40714688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91973253-A-G

40714745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91973305-C-T

40714977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91973539-G-A

40715157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91973717-A-G

http://identifiers.org/hco/12/GRCh38#40715425-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#91974568-A-C

40715515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91974617-T-C

40715517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91974619-A-G

http://identifiers.org/hco/12/GRCh38#40715525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#91974628-C-A

40715565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91974668-T-C

40715613-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91974716-G-C

40715658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91974763-G-T

40715721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91974829-G-A

40715786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91974892-C-T

40715864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91974972-C-T

40715885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91974992-G-A

http://identifiers.org/hco/12/GRCh38#40716020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#91975092-C-A

40716090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91975159-G-T

40719593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91976230-T-C

40719734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91976371-T-C

40720358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91976616-T-C

40720416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91976691-G-T

40720428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91976703-A-G

40720428-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91976703-A-T

40720478-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91976788-G-C

40720500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91976810-T-C

40721113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91977070-T-C

40721225-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91977167-C-G

40721281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91977221-C-T

http://identifiers.org/hco/12/GRCh38#40721506-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#91977429-A-C

40722147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91977565-C-T

40722292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91977679-T-C

40722627-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91977961-C-G

40722709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91978041-A-G

40722798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91978109-A-G

40722815-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91978126-G-C

40722877-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91978161-G-C

http://identifiers.org/hco/12/GRCh38#40722929-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#91978208-A-C

40723426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91978689-C-T

40723491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91978754-A-G

40723527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91978792-G-A

40723527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91978792-G-T

40724169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91979306-C-T

40724448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91979487-A-G

40724601-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91979631-A-T

40724649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91979676-A-G

40724762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91979987-T-C

40724765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91979990-C-T

40724887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91980133-G-A

40724898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91980144-G-A

40724927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91980173-G-T

40726774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91980417-A-G

40727089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91980499-T-C

40727098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91980508-A-G

40727205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91980611-G-A

40727205-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91980611-G-C

40727246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91980649-A-G

40727326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91980716-C-T

40727346-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91980736-T-G

40727671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91981053-T-C

40727706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91981084-C-T

http://identifiers.org/hco/12/GRCh38#40727712-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#91981090-A-C

40727977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91981316-G-A

40728109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91981450-G-A

40728176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91981517-A-G

40728256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91981574-C-T

40728398-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91981677-A-T

http://identifiers.org/hco/12/GRCh38#40731775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#91983028-C-A

40732112-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91983359-A-T

40732321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91983582-A-G

http://identifiers.org/hco/12/GRCh38#40732888-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#91984117-A-C

40732903-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91984130-C-G

40732910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91984137-T-C

40732922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91984146-G-A

40733026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91984684-G-A

40733210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91984855-C-T

40734124-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, undefined
orthologous variants: 91985677-C-G

40734131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, undefined
orthologous variants: 91985684-A-G

http://identifiers.org/hco/12/GRCh38#40734353-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#91985901-A-C

40734475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91985993-G-A

40734478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91985996-A-G

40734480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91985998-C-T

40734485-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91986002-A-T

40734531-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91986050-G-C

http://identifiers.org/hco/12/GRCh38#40734553-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#91986070-A-C

40734557-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91986074-T-G

40734895-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91986315-C-G

40735538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91986970-A-G

40735538-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91986970-A-T

40735579-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91987006-C-G

40735655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91987064-G-A

40735752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91987144-T-C

40735779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91987169-G-A

40735913-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91987288-G-C

40742314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91990231-A-G

40742726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91990545-T-C

40742934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91990719-A-G

40743058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91990976-C-T

40743059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91990977-G-A

40743059-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91990977-G-C

40743068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91990984-G-A

40743068-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91990984-G-C

40743089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91991005-A-G

40743131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91991048-G-A

40743177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91991099-G-A

40743178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91991100-G-A

40743244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91991166-G-A

40743315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91991233-G-A

40743485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91991399-A-G

40743501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91991415-T-C

40751587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91997287-T-C

40751733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91997423-G-A

40751925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91997560-G-A

http://identifiers.org/hco/12/GRCh38#40751984-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#91997613-A-C

40752045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91997673-T-C

40752162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91997792-C-T

40752178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91997809-A-G

40752243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91997872-C-T

40752245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91997874-C-T

http://identifiers.org/hco/12/GRCh38#40752409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#91998025-C-A

40752453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91998063-G-T

40752626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91998223-G-A

40752633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91998230-T-C

40753154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91998714-C-T

40753353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91998927-C-T

http://identifiers.org/hco/12/GRCh38#40753358-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#91998932-A-C

40753358-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91998932-A-T

40753978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 91999515-T-C

40758021-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92000011-C-G

40758153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92000165-C-T

40758176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92000187-G-A

40758176-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92000187-G-C

40758181-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92000192-C-G

40758251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92000261-T-C

40758284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92000294-G-T

40758302-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92000312-T-G

http://identifiers.org/hco/12/GRCh38#40758376-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92000378-C-A

40758376-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92000378-C-G

40758376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92000378-C-T

40761181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92003924-T-C

40761202-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92003945-G-C

40761273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92004021-A-G

http://identifiers.org/hco/12/GRCh38#40761381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92004121-C-A

40761417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92004159-G-A

40761627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92004361-G-A

40761701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92004424-T-C

40761973-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92004611-T-G

40762028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92004664-C-T

40762173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92004794-A-G

40762425-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92005030-A-T

40762442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92005048-C-T

40762473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92005079-T-C

40762555-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92005158-T-A

40762674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92005314-A-G

40762755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92005359-A-G

40762798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92005405-A-G

http://identifiers.org/hco/12/GRCh38#40762811-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92005418-A-C

40762814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92005421-A-G

40763348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92005516-G-A

http://identifiers.org/hco/12/GRCh38#40763370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92005538-C-A

40763388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92005556-G-A

40763454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92005611-C-T

40763597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92005751-G-A

40763723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92005875-G-A

http://identifiers.org/hco/12/GRCh38#40763731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92005883-C-A

40763770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92005914-C-T

40767877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92009778-T-C

40767934-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92009834-C-G

40768086-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92009942-G-T

http://identifiers.org/hco/12/GRCh38#40768104-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92009967-A-C

http://identifiers.org/hco/12/GRCh38#40768314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92010164-C-A

40768314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92010164-C-T

40768443-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92010277-C-G

40769202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92012556-A-G

http://identifiers.org/hco/12/GRCh38#40769381-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92012723-A-C

40769981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92013120-C-T

40770001-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92013140-T-A

40770940-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92013777-T-G

40770948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92013785-C-T

40770986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92013823-A-G

40771242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92014051-G-A

40771310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92014116-G-A

http://identifiers.org/hco/12/GRCh38#40771417-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92014211-A-C

40772193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92014779-C-T

40772194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92014780-G-A

http://identifiers.org/hco/12/GRCh38#40772313-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92014900-C-A

40772503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92015090-G-A

40772504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92015091-C-T

40772505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92015092-G-A

40772505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92015092-G-T

40772509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92015095-T-C

40772664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92015249-G-T

40772853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92015412-G-T

40773526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92018186-G-A

40775893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92019082-C-T

40775944-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92019118-C-G

40775998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92019169-T-C

40776090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92019256-G-A

40776139-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92019305-T-G

40776234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92019399-A-G

40776285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92019457-A-G

40776285-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92019457-A-T

40779237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92019864-G-T

40779274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92019901-G-A

40779284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92019914-G-T

40779426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92020040-G-T

40779456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92020070-G-A

40779526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92020138-C-T

40779663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92020253-T-C

40779740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92020355-G-A

40779766-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92020392-T-A

40779795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92020421-T-C

40779806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92020428-A-G

40779807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92020429-G-A

40779955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92020573-C-T

http://identifiers.org/hco/12/GRCh38#40780055-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92020659-A-C

40780137-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92020744-G-C

40780219-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92020923-G-C

40780729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92021607-C-T

40780825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92021700-G-A

40780909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92021779-T-C

40781029-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92021887-A-T

40781087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92021944-G-A

40781490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92022447-T-C

40781530-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92022482-T-A

40781723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92022666-T-C

40781758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92022697-G-A

http://identifiers.org/hco/12/GRCh38#40781788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92022727-C-A

http://identifiers.org/hco/12/GRCh38#40781922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92022855-C-A

http://identifiers.org/hco/12/GRCh38#40782117-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92023085-A-C

40782117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92023085-A-G

http://identifiers.org/hco/12/GRCh38#40782283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92023267-C-A

40782404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92023386-C-T

40782503-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92023471-C-G

40782547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92023513-A-G

40782547-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92023513-A-T

http://identifiers.org/hco/12/GRCh38#40782713-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92024411-A-C

http://identifiers.org/hco/12/GRCh38#40782835-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92024507-A-C

http://identifiers.org/hco/12/GRCh38#40782839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92024512-C-A

40782839-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92024512-C-G

40782839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92024512-C-T

http://identifiers.org/hco/12/GRCh38#40783076-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92024719-A-C

40783228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92024901-G-A

40783277-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92024947-C-G

40783342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92025002-A-G

40783664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92025284-A-G

40784068-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92025708-A-T

40784237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92025892-T-C

40784342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92026527-A-G

40784346-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92026531-T-G

40784409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92026588-A-G

40784467-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92026669-T-G

40784557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92026754-A-G

http://identifiers.org/hco/12/GRCh38#40784725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92026896-C-A

40784800-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92026966-C-G

40784942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92027067-G-A

40786059-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92027562-C-G

http://identifiers.org/hco/12/GRCh38#40786100-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92027603-A-C

40786100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92027603-A-G

40786256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92027736-C-T

40786258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92027738-G-T

40786339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92027814-T-C

40786566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92028176-T-C

40786664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92028274-A-G

40786826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92028448-A-G

40786867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92028489-A-G

40786938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92028550-G-A

40787111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92028647-C-T

40787221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92028749-T-C

40787245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92028772-C-T

40787298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92028820-T-C

40787327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92028848-G-T

40788189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92029613-G-A

http://identifiers.org/hco/12/GRCh38#40788461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92029884-C-A

40788463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92029886-T-C

40788645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92030049-C-T

40788949-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92030840-A-T

40788994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92030885-G-A

40789018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92030912-G-A

40789160-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92031050-A-T

40789349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92031232-A-G

40789413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92031285-G-A

40789662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92031603-A-G

40789877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92031798-A-G

40790563-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92032491-T-G

40790599-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92032526-C-G

http://identifiers.org/hco/12/GRCh38#40790658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92032585-C-A

40790658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92032585-C-T

40790714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92032640-G-A

40791235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92033103-T-C

40791263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92033131-G-A

40791269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92033137-G-A

40792818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92033566-A-G

40793487-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92034148-T-A

40793600-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92034259-C-G

40793604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92034263-A-G

40793623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92034282-A-G

40793624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92034283-G-A

40793668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92034326-C-T

40793679-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92034337-T-A

40793738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92034393-G-A

http://identifiers.org/hco/12/GRCh38#40793933-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92034746-A-C

40793933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92034746-A-G

40794053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92034845-C-T

40794137-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92034931-T-A

40794170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92034964-A-G

40794184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92034977-G-A

40794571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92035376-A-G

40795752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92037298-T-C

40796095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92037604-T-C

40796152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92037660-T-C

40796277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92037781-T-C

40796277-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92037781-T-G

40796394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92037886-A-G

http://identifiers.org/hco/12/GRCh38#40796461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92037952-C-A

40796483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92037976-T-C

40796560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92038027-A-G

40796629-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92038074-T-G

40796764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92038209-A-G

http://identifiers.org/hco/12/GRCh38#40796776-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92038221-A-C

40796789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92038236-G-A

40796793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92038240-C-T

40796823-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92038270-G-C

40796999-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92038464-C-G

http://identifiers.org/hco/12/GRCh38#40797063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92038529-C-A

40797150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92038601-A-G

40797481-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92038826-A-T

40797624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92038970-G-A

40797795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92039113-C-T

40799570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92040333-A-G

40799965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92040661-G-A

40806315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92044965-T-C

40806392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92045030-C-T

40806420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92045065-G-A

40806571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92045205-G-T

40806575-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92045209-C-G

40806575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92045209-C-T

40806747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92045357-C-T

40806818-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92045409-T-G

40806982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92045578-G-A

40807054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92045651-G-A

40807060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92045657-G-A

40807097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92045694-A-G

40807228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92046603-C-T

40807382-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92046736-C-G

40807466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92046820-G-T

40807485-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92046839-C-G

40807500-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92046854-A-T

40807551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92046928-A-G

40807581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92047130-T-C

40807651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92047219-C-T

40807660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92047228-A-G

40808886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92048293-A-G

40809048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92048462-T-C

40809141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92048552-A-G

40809162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92048573-C-T

40809195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92048608-A-G

40809350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92048762-C-T

40809389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92048801-G-T

40820449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92052145-T-C

40820449-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92052145-T-G

40820742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92052460-G-T

40821160-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92052874-T-G

40821307-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92053020-T-G

40821346-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92053053-T-A

40821605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92053309-A-G

40823649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92054379-C-T

40823672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92054402-C-T

40823722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92054448-C-T

http://identifiers.org/hco/12/GRCh38#40823750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92054476-C-A

http://identifiers.org/hco/12/GRCh38#40823755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92054481-C-A

40823766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92054492-A-G

40823814-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92054539-C-G

40823883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92054729-C-T

40823960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92054806-G-A

40824155-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92054988-A-T

http://identifiers.org/hco/12/GRCh38#40824722-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92055803-A-C

40824902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92055975-G-A

40824902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92055975-G-T

http://identifiers.org/hco/12/GRCh38#40824903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92055976-C-A

40824903-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92055976-C-G

40824921-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92055994-A-T

40825066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92056143-C-T

http://identifiers.org/hco/12/GRCh38#40825272-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92056322-A-C

http://identifiers.org/hco/12/GRCh38#40825422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92056501-C-A

40825422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92056501-C-T

40825475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92056547-T-C

40825528-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92056599-A-T

40825529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92056600-C-T

40825651-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92056735-T-A

40825706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92056790-A-G

40825710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92056794-T-C

40825753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92056830-C-T

40825938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92057000-G-A

http://identifiers.org/hco/12/GRCh38#40826217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92057238-C-A

40826244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92057274-T-C

40826261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92057331-A-G

40826615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92057876-G-A

40826615-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92057876-G-C

40826644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92057905-C-T

40826803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92058057-A-G

http://identifiers.org/hco/12/GRCh38#40827205-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92058449-A-C

40828077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92059315-G-T

40828088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92059326-A-G

40828133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92059374-A-G

40828135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92059376-G-T

40828146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92059387-C-T

40828148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92059389-G-A

40828148-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92059389-G-T

40828403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92059639-G-A

40828665-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92059908-T-A

40828665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92059908-T-C

40828817-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92060056-G-C

40828848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92060087-A-G

40828977-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92060345-T-G

40829073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92060405-A-G

40829075-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92060407-A-T

40829313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92060619-C-T

40829357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92060652-A-G

40829470-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92060734-T-A

40829561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92060814-T-C

http://identifiers.org/hco/12/GRCh38#40829562-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92060815-A-C

40829562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92060815-A-G

40829600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92060863-A-G

40829632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92060897-G-A

40829730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92060992-G-A

40829823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92061061-T-C

40829824-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92061062-G-C

40829824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92061062-G-T

40831210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92061690-T-C

http://identifiers.org/hco/12/GRCh38#40831444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92061906-C-A

40831444-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92061906-C-G

40833972-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92063865-T-G

40834290-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92064179-T-A

40834290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92064179-T-C

40834541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92064400-G-A

40834587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92064445-G-A

40834587-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92064445-G-C

40834602-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92064460-C-G

40834602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92064460-C-T

40834846-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92064690-T-A

40834902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92064749-A-G

40834984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92064828-G-T

40835324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92065158-T-C

40835436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92065265-G-A

40835436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92065265-G-T

http://identifiers.org/hco/12/GRCh38#40836417-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92065981-A-C

40836417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92065981-A-G

40836639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92066209-C-T

40836742-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92066275-C-G

40836742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92066275-C-T

http://identifiers.org/hco/12/GRCh38#40836938-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92066350-A-C

40837010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92066423-C-T

http://identifiers.org/hco/12/GRCh38#40837027-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92066439-A-C

http://identifiers.org/hco/12/GRCh38#40842209-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92066731-A-C

40842720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92066988-G-A

40842803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92067083-T-C

40842875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92067151-G-T

40842923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92067197-A-G

40842952-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92067220-T-A

40842952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92067220-T-C

40842952-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92067220-T-G

40843048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92067310-G-A

40843074-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92067335-C-G

40843085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92067346-A-G

40843086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92067347-C-T

40843101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92067362-A-G

40843111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92067372-A-G

40843231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92067451-T-C

40843253-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92067473-T-A

40843407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92067633-G-A

40843503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92068116-C-T

http://identifiers.org/hco/12/GRCh38#40843657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92068495-C-A

40843695-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92068533-A-T

40843702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92068540-A-G

http://identifiers.org/hco/12/GRCh38#40843813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92068684-C-A

40843859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92068808-C-T

http://identifiers.org/hco/12/GRCh38#40844036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92068979-C-A

40844036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92068979-C-T

40844560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92069213-A-G

40844954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92069299-G-A

40844954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92069299-G-T

40851308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92069864-G-A

40851339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92069899-C-T

40851466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92070013-A-G

40851565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92070082-A-G

40852905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92071314-G-T

40852996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92071394-G-A

40853347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92071718-G-A

40853355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92071723-A-G

40853577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92071947-A-G

40853634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92071990-A-G

40853634-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92071990-A-T

40853674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92072016-C-T

40853729-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92072069-T-A

40853729-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92072069-T-G

40853790-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92072119-C-G

40853790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92072119-C-T

40853811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92072137-T-C

40853814-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92072140-C-G

40868411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92077237-G-A

http://identifiers.org/hco/12/GRCh38#40868453-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92077268-A-C

http://identifiers.org/hco/12/GRCh38#40868558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92077364-C-A

40868558-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92077364-C-G

http://identifiers.org/hco/12/GRCh38#40868561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92077367-C-A

40868561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92077367-C-T

http://identifiers.org/hco/12/GRCh38#40868629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92077414-C-A

40868629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92077414-C-T

http://identifiers.org/hco/12/GRCh38#40868709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92077480-C-A

40868749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92077521-T-C

40868760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92077535-G-A

40868768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92077540-A-G

40868818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92077579-A-G

http://identifiers.org/hco/12/GRCh38#40868827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92077588-C-A

40868913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92077685-A-G

40869225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92077948-T-C

40869259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92077982-C-T

40872918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92079092-T-C

40872947-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92079120-T-G

40873008-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92079181-A-T

40873107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92079227-A-G

40873113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92079233-T-C

40873191-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92079290-G-C

40873641-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92079705-A-T

40873644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92079708-C-T

40873741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92079806-T-C

40878849-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92082803-C-G

40879043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92083002-C-T

40879066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92083025-G-A

http://identifiers.org/hco/12/GRCh38#40879096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92083055-C-A

40879096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92083055-C-T

40879352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92083281-C-T

40879364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92083291-A-G

40879379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92083306-A-G

40879618-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92083589-A-T

40879773-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92083718-T-G

40880056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92085616-G-A

40880161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92085710-G-A

40880278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92085802-G-A

40880311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92085834-G-A

40880558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92086151-T-C

40880589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92086180-T-C

40880624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92086215-C-T

40880699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92086274-T-C

40880758-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92086316-C-G

40882316-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92086455-A-T

40882342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92086482-C-T

40882409-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92086550-G-C

40882411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92086552-T-C

40882571-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92086693-A-T

40882572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92086694-G-A

40882611-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92086726-C-G

40882918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92088363-T-C

40882918-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92088363-T-G

40882927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92088377-C-T

40882977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92088424-C-T

40882996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92088450-A-G

http://identifiers.org/hco/12/GRCh38#40883014-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92088469-A-C

40883463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92088874-A-G

40883554-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92088963-A-T

40883655-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92089060-G-C

40883722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92089616-T-C

40883731-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92089620-A-T

40883732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92089621-A-G

40883746-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92089635-T-G

40883838-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92089728-T-A

40884026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92089907-G-T

40884281-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92090322-T-A

40884311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92090348-G-T

http://identifiers.org/hco/12/GRCh38#40884437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92090469-C-A

http://identifiers.org/hco/12/GRCh38#40884541-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92090571-A-C

40884546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92090576-G-T

40884577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92090605-G-A

http://identifiers.org/hco/12/GRCh38#40888486-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92093903-A-C

40888486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92093903-A-G

40888568-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92093955-T-G

http://identifiers.org/hco/12/GRCh38#40888612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92094003-C-A

40888703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92094597-C-T

http://identifiers.org/hco/12/GRCh38#40888900-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92094797-A-C

40889024-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92094898-A-T

40889069-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92094927-T-A

40889275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92095114-G-T

40898600-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92098092-T-A

40898628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92098124-T-C

40898671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92098171-A-G

40898671-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92098171-A-T

40898678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, undefined
orthologous variants: 92098178-A-G

40898790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92098288-G-A

40898790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92098288-G-T

http://identifiers.org/hco/12/GRCh38#40898852-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92098352-A-C

40899101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92098589-A-G

40899129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92098617-C-T

40899148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92098638-G-A

40899336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92098832-A-G

http://identifiers.org/hco/12/GRCh38#40899384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92098875-C-A

40899558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92099414-A-G

40899609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92099464-G-A

40899684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92099527-C-T

40900004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92099833-C-T

40900008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92099837-G-A

40901858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92101307-G-A

40901875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92101326-G-A

40901989-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92101427-T-G

40902018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92101449-A-G

40902228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92101603-C-T

http://identifiers.org/hco/12/GRCh38#40902232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92101607-C-A

40902380-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92101750-G-C

40902498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92101899-A-G

40902498-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92101899-A-T

40902518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92101923-G-A

40902837-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92102209-G-C

40903249-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92106690-C-G

40903250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92106691-G-A

40903250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92106691-G-T

40903387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92106825-G-T

http://identifiers.org/hco/12/GRCh38#40903413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92106843-C-A

40903413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92106843-C-T

40903483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92106911-G-A

40903964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92107335-C-T

40905279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92109495-T-C

40905646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92109821-A-G

40905688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92109861-T-C

http://identifiers.org/hco/12/GRCh38#40905919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92110070-C-A

40905919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92110070-C-T

40905923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92110074-A-G

40905951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92110105-A-G

40905971-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92110125-T-G

40907034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92112814-T-C

40907035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92112815-G-T

40907062-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92112838-A-T

http://identifiers.org/hco/12/GRCh38#40907067-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92112843-A-C

40907079-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, undefined
orthologous variants: 92112855-G-C

40907191-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, undefined
orthologous variants: 92112952-A-T

40907370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, undefined
orthologous variants: 92113119-T-C

40907547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, undefined
orthologous variants: 92113293-A-G

40907709-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92113451-T-G

40907748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92113505-A-G

40907837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92113632-A-G

40908115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92113945-T-C

40908115-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92113945-T-G

40908240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92114039-A-G

40908243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92114042-G-T

40908250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92114049-A-G

40908274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92114068-T-C

40908274-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92114068-T-G

40908297-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92114103-T-G

40908301-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92114108-T-A

40908301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92114108-T-C

http://identifiers.org/hco/12/GRCh38#40908306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92114113-C-A

40908306-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92114113-C-G

40908306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92114113-C-T

40908329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92114143-C-T

40908341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92114181-T-C

http://identifiers.org/hco/12/GRCh38#40908483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92114318-C-A

40908483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: synonymous variant
orthologous variants: 92114318-C-T

40908510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92114345-G-T

40908530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92114365-G-A

http://identifiers.org/hco/12/GRCh38#40908532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92114367-C-A

40908532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92114367-C-T

http://identifiers.org/hco/12/GRCh38#40908548-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92114383-C-A

40908548-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92114383-C-G

40908548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92114383-C-T

http://identifiers.org/hco/12/GRCh38#40908628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92114474-C-A

40908628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92114474-C-T

40908883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92114683-C-T

40908951-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92114746-T-A

40909008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92114807-G-A

40909287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92115062-C-T

http://identifiers.org/hco/12/GRCh38#40909289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92115064-C-A

40909289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92115064-C-T

40909628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92115746-A-G

40909698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92118000-T-C

40909718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92118020-C-T

40909875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92118149-T-C

40909875-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92118149-T-G

40909958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92118227-T-C

http://identifiers.org/hco/12/GRCh38#40910022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92118273-C-A

40910022-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92118273-C-G

40910022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92118273-C-T

40910110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92118365-G-A

40910133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92118405-A-G

40910133-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92118405-A-T

40910135-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92118407-A-T

http://identifiers.org/hco/12/GRCh38#40910139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92118411-C-A

40910140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92118441-T-C

http://identifiers.org/hco/12/GRCh38#40910155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92118456-C-A

40910155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92118456-C-T

40910207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92118507-G-T

40910226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92118526-G-A

40910226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92118526-G-T

40910485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92119057-G-A

40910485-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92119057-G-C

40910529-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92119101-A-T

40910704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92119250-T-C

40910753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92119290-T-C

40910835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92119376-C-T

http://identifiers.org/hco/12/GRCh38#40910882-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92119415-A-C

40910882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92119415-A-G

40913018-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92121555-T-G

40913155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92121681-T-C

40913218-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92121733-T-A

40913247-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92121762-C-G

40913285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92121803-T-C

40913286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92121805-G-T

40913384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92121892-T-C

40913510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92122020-T-C

http://identifiers.org/hco/12/GRCh38#40913512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92122022-C-A

40913628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92122135-G-A

40913733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92122239-G-A

40913810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92122323-A-G

40913847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92122360-T-C

40913942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92122464-G-T

40913946-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92122468-T-G

40914036-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92122541-C-G

40914257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92122674-G-A

40914320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92122746-C-T

40914480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92122870-A-G

40914530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92122920-A-G

40914736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92123060-A-G

40917677-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92125410-C-G

40917733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92125466-A-G

40917773-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92125507-T-G

http://identifiers.org/hco/12/GRCh38#40917815-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92125552-A-C

http://identifiers.org/hco/12/GRCh38#40917868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92125612-C-A

40918057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92125786-T-C

40918233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92125965-G-A

40918354-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92126072-T-G

40918355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92126073-G-A

40918571-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92126432-T-A

http://identifiers.org/hco/12/GRCh38#40918601-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92126462-A-C

40918601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92126462-A-G

40918622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92126481-T-C

40918667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: synonymous variant
orthologous variants: 92126532-A-G

40918835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92126704-A-G

http://identifiers.org/hco/12/GRCh38#40918862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92126727-C-A

40918874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92126747-T-C

http://identifiers.org/hco/12/GRCh38#40918876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92126749-C-A

40918876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92126749-C-T

40918899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92126772-G-A

40918899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92126772-G-T

http://identifiers.org/hco/12/GRCh38#40918900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92126773-C-A

40918900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92126773-C-T

http://identifiers.org/hco/12/GRCh38#40918901-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92126774-A-C

40918901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92126774-A-G

http://identifiers.org/hco/12/GRCh38#40918908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92126781-C-A

40918908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92126781-C-T

40919034-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92126880-T-G

http://identifiers.org/hco/12/GRCh38#40919142-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92126978-A-C

http://identifiers.org/hco/12/GRCh38#40919178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92127016-C-A

40919233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92127073-C-T

40919310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92127242-T-C

40919402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92127335-A-G

40919405-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92127338-C-G

40919415-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92127351-C-G

40919415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92127351-C-T

40919499-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92127438-C-G

40919513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92127452-G-A

http://identifiers.org/hco/12/GRCh38#40919617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92127554-C-A

40919617-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92127554-C-G

40919663-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92127600-C-G

40919663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92127600-C-T

40919740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92127675-G-A

40919778-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92127711-T-G

40919860-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92127778-A-T

40919900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92127814-T-C

http://identifiers.org/hco/12/GRCh38#40920026-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92127926-A-C

40920062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92127960-A-G

40920149-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92128010-G-C

40920195-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92128033-C-G

40920195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92128033-C-T

40920498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92128301-G-A

40920616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92128397-A-G

40921026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92128799-C-T

40921112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92128866-G-A

40921112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92128866-G-T

40921289-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, undefined
orthologous variants: 92129027-C-G

40921289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, undefined
orthologous variants: 92129027-C-T

40921746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92129457-G-A

40921982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92129718-C-T

40922034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92129771-G-A

40922126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92129857-A-G

40922126-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92129857-A-T

40922143-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92129873-A-T

40922161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92129891-G-A

40922161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92129891-G-T

40922178-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92129908-A-T

40922198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92129928-C-T

40922200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92129930-G-A

40922200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92129930-G-T

40922219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92129946-T-C

40922219-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92129946-T-G

40922323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: missense variant
orthologous variants: 92130049-G-T

40922376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: synonymous variant
orthologous variants: 92130102-A-G

40922388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: synonymous variant
orthologous variants: 92130114-C-T

40923263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92131270-A-G

40923302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92131309-T-C

40923344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92131358-G-A

40923344-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92131358-G-C

http://identifiers.org/hco/12/GRCh38#40923364-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92131377-C-A

40924004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92131989-T-C

40924029-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92132067-C-G

40924029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92132067-C-T

40924452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92132222-G-T

http://identifiers.org/hco/12/GRCh38#40924502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92132256-C-A

40924502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92132256-C-T

40924657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92132406-A-G

40924678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92132418-T-C

40924680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92132420-G-A

40924680-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92132420-G-T

http://identifiers.org/hco/12/GRCh38#40924681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92132421-C-A

40924681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92132421-C-T

40924692-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92132432-C-G

40924692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92132432-C-T

40924699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92132439-G-A

40924723-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92132462-T-A

40924723-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92132462-T-G

40924724-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92132463-A-T

40924746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92132502-T-C

40924794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92132542-G-A

40924857-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92132977-T-A

40924871-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92132991-A-T

40924879-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92132999-A-T

40924932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92133047-G-A

40924932-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92133047-G-C

40924932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92133047-G-T

40924938-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92133053-T-A

40924938-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92133053-T-G

40924945-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92133061-A-T

40925688-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92133650-C-G

http://identifiers.org/hco/12/GRCh38#40925751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92133708-C-A

40925794-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92133749-T-G

http://identifiers.org/hco/12/GRCh38#40925890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92133769-C-A

40925890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92133769-C-T

http://identifiers.org/hco/12/GRCh38#40926088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92133930-C-A

40926107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92133949-G-T

http://identifiers.org/hco/12/GRCh38#40926310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92134086-C-A

40926310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92134086-C-T

40927251-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92136609-T-G

40927647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92136974-A-G

40927664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92136991-A-G

40927774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92137086-C-T

40927837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92137150-G-A

40927912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92137208-C-T

http://identifiers.org/hco/12/GRCh38#40927913-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92137209-A-C

40928559-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92137773-G-C

40928667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92137862-G-T

40928668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92137863-T-C

40929127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92138242-T-C

http://identifiers.org/hco/12/GRCh38#40929312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92140309-C-A

http://identifiers.org/hco/12/GRCh38#40929317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92140314-C-A

40929317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92140314-C-T

40929337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92140335-C-T

http://identifiers.org/hco/12/GRCh38#40929356-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92140342-A-C

40929367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92140353-T-C

40929396-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92140380-T-A

http://identifiers.org/hco/12/GRCh38#40929412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92140396-C-A

40929434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92140415-C-T

40929530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92140508-C-T

40929688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92140671-A-G

40929688-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92140671-A-T

40929703-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92140686-A-T

40929710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92140693-G-A

40929710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92140693-G-T

40929918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: missense variant
orthologous variants: 92140894-G-A

40930018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92140995-G-A

40930018-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92140995-G-C

40930107-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92141063-G-C

40930129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92141080-G-A

40930129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92141080-G-T

40930136-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92141087-G-C

40930488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92141407-A-G

40930596-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92141560-G-C

40930681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92141651-A-G

40931183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92142055-T-C

40931205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92142081-T-C

40931406-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92142266-C-G

40931406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92142266-C-T

40931543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92142391-C-T

40931600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92142446-C-T

40931654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92142503-G-T

40932567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92142800-C-T

40932670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92142897-A-G

40933114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92143295-C-T

http://identifiers.org/hco/12/GRCh38#40933167-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92143348-A-C

http://identifiers.org/hco/12/GRCh38#40933318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92143476-C-A

40933318-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92143476-C-G

40933318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92143476-C-T

40933324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92143482-A-G

http://identifiers.org/hco/12/GRCh38#40933336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92143494-C-A

40933336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92143494-C-T

http://identifiers.org/hco/12/GRCh38#40933448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92143596-C-A

40933448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92143596-C-T

40933507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: synonymous variant
orthologous variants: 92143655-T-C

40933507-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: missense variant
orthologous variants: 92143655-T-G

40933513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: synonymous variant
orthologous variants: 92143661-T-C

40933610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92143770-A-G

40933644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92143788-G-A

40933644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92143788-G-T

40933670-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92143815-T-G

40933682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92143827-A-G

40933751-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: synonymous variant
orthologous variants: 92143896-T-A

40933762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: missense variant
orthologous variants: 92143907-C-T

http://identifiers.org/hco/12/GRCh38#40933763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92143908-C-A

40933817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: synonymous variant
orthologous variants: 92143962-T-C

40933918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92144058-A-G

40933933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92144073-A-G

40934012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92144152-A-G

40934012-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92144152-A-T

40934210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92144316-A-G

40934298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92144408-G-A

40934338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92144446-G-A

40934338-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92144446-G-C

40934559-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92144860-C-G

40935711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92147366-A-G

40935778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92147432-G-T

http://identifiers.org/hco/12/GRCh38#40936169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92147820-C-A

40936169-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92147820-C-G

40936476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92148251-A-G

40936557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92148362-A-G

http://identifiers.org/hco/12/GRCh38#40936672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92148643-C-A

40936672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92148643-C-T

40936722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92148693-G-A

40936722-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92148693-G-C

40936782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 92148741-A-G

40936803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: synonymous variant
orthologous variants: 92148762-C-T

40936996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92148924-T-C

40937231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92149948-G-A

40937444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92150154-T-C

40937487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92150197-G-A

40937487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92150197-G-T

http://identifiers.org/hco/12/GRCh38#40937498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92150208-C-A

40937498-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92150208-C-G

40937554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92150259-A-G

40937644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: synonymous variant
orthologous variants: 92150352-C-T

40937710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92150418-G-A

40937710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92150418-G-T

40937754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92150467-A-G

40937759-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92150470-G-C

40937784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92150497-G-A

40937784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92150497-G-T

40937882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92150770-A-G

40937994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92150878-T-C

40938170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92151024-G-A

40938213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92151067-A-G

40938319-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92151176-T-G

40938382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92151240-G-T

40938508-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92151325-G-C

40938722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92151530-C-T

40939188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92151665-G-T

http://identifiers.org/hco/12/GRCh38#40939265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92151723-C-A

40939283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92151741-G-A

40939331-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 92151787-T-G

40939462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: synonymous variant
orthologous variants: 92151918-A-G

40939474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: synonymous variant
orthologous variants: 92151930-C-T

40942075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92152889-A-G

40942113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92152926-G-T

40942333-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92153136-A-T

40942336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92153139-A-G

40943433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92153572-T-C

40943552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92153687-T-C

40943648-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: missense variant
orthologous variants: 92153779-T-A

40943705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: synonymous variant
orthologous variants: 92153836-T-C

40943763-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92154044-T-G

40943768-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92154049-A-T

http://identifiers.org/hco/12/GRCh38#40943840-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92154122-A-C

40943840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92154122-A-G

40943843-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92154125-T-A

40943861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92154143-G-A

40943863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92154145-T-C

40943879-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92154160-T-A

40943882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92154163-A-G

40943907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92154191-A-G

40943916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92154200-T-C

40943933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92159286-A-G

40943955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92159308-A-G

40943970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92159324-G-A

40943970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92159324-G-T

http://identifiers.org/hco/12/GRCh38#40943979-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92159338-A-C

40943979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92159338-A-G

http://identifiers.org/hco/12/GRCh38#40944201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92159566-C-A

40944211-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92159576-T-A

40944225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92159590-A-G

40945088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92161141-G-A

40945200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92161284-G-A

40945514-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92161611-T-A

40945537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92161633-A-G

40945878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92162452-A-G

40946012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92162569-A-G

40946105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92162667-A-G

http://identifiers.org/hco/12/GRCh38#40946127-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92162686-A-C

40946145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92162704-T-C

40946380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92163000-T-C

40946430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92163050-G-T

40946518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92163119-A-G

40946852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92163406-G-A

http://identifiers.org/hco/12/GRCh38#40946905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92163456-C-A

40946908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92163459-C-T

40947388-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92164191-T-G

40947584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92164424-T-C

40951236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92165700-A-G

40951380-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92165778-A-T

40951452-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92165843-C-G

40953313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92166895-A-G

40953470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92167051-T-C

40953766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92167433-A-G

40953792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92167459-G-A

40953828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92167495-G-A

40953882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92167550-A-G

40959109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 92169110-A-G

40959179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: synonymous variant
orthologous variants: 92169180-C-T

40959185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: synonymous variant
orthologous variants: 92169186-C-T

40959355-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92169361-A-T

40959544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92169523-G-A

40959823-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92169842-G-C

40959972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92169985-T-C

40960002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92170006-T-C

http://identifiers.org/hco/12/GRCh38#40960045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92170049-C-A

40960272-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92170252-C-G

40960306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92170274-A-G

40960379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92170358-A-G

40960379-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92170358-A-T

http://identifiers.org/hco/12/GRCh38#40960514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92170492-C-A

40960911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92170857-G-A

40961093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92171009-T-C

40962021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92171548-G-A

40962088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92171612-C-T

40962247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92171758-A-G

http://identifiers.org/hco/12/GRCh38#40962277-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92171788-A-C

40962496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92172786-G-A

40962873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92173105-A-G

40962902-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92173134-G-C

40962902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92173134-G-T

40962936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92173168-G-A

40962942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92173174-T-C

40962985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92173211-G-A

40963338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92176824-G-T

40965765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92178603-G-A

40965770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92178609-A-G

40965800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92178644-A-G

40965800-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92178644-A-T

http://identifiers.org/hco/12/GRCh38#40965803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92178647-C-A

40965920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92178748-G-A

40965974-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92178789-T-G

40966153-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92178942-T-G

40966173-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92178962-T-G

40966180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92178969-A-G

40966348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92179138-A-G

http://identifiers.org/hco/12/GRCh38#40966643-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92179446-A-C

http://identifiers.org/hco/12/GRCh38#40966675-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92179478-A-C

40968608-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92180605-C-G

40968635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92180636-G-A

40968935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92180888-C-T

40969011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92180962-G-T

40969098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92181041-A-G

40969262-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92181214-T-G

40969348-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92181295-T-A

40969376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92181309-C-T

40969642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92181660-G-T

40971233-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92183250-G-T

http://identifiers.org/hco/12/GRCh38#40971283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92183300-C-A

40971292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92183309-G-A

40971292-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92183309-G-C

40971324-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92183328-T-A

40971557-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 92183559-A-T

http://identifiers.org/hco/12/GRCh38#40971558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92183560-C-A

40971647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 92183643-T-C

40971723-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 92183717-G-T

40971827-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 92183793-A-T

40971967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 92183934-A-G

40971973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 92183940-G-T

http://identifiers.org/hco/12/GRCh38#40972015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92183986-C-A

40972015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 92183986-C-T

http://identifiers.org/hco/12/GRCh38#40972016-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92183987-A-C

40972016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 92183987-A-G

40972016-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 92183987-A-T

40972101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 92184064-G-A

40972101-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 92184064-G-T

40972173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 92184114-A-G

http://identifiers.org/hco/12/GRCh38#40972239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92184183-C-A

40972239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 92184183-C-T

40972288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 92184228-G-A

http://identifiers.org/hco/12/GRCh38#40972408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92184319-C-A

40972408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 92184319-C-T

40972525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 92184442-T-C

40972665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 92184551-A-G

http://identifiers.org/hco/12/GRCh38#40972721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92184581-C-A

40972721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92184581-C-T

40972803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92184665-T-C

40976270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92185990-G-A

40976461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92186176-C-T

40976474-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92186189-A-T

40976517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92186241-G-A

40976544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92186268-A-G

40976555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92186279-A-G

40976556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92186280-G-A

40976695-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92186439-C-G

40976696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92186440-A-G

40976788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92186524-G-A

40978415-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92187156-T-A

40978437-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92187175-T-A

40978513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92187240-T-C

http://identifiers.org/hco/12/GRCh38#40978893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92187638-C-A

40978893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 92187638-C-T

40978928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 92187677-T-C

http://identifiers.org/hco/12/GRCh38#40978939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92187688-C-A

40979118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 92187854-T-C

40979206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 92187937-A-G

40979236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 92187970-C-T

40979338-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92188030-T-G

40979688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92188298-T-C

40979975-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92188618-T-G

40980782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, undefined
orthologous variants: 92189389-G-A

40980782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, undefined
orthologous variants: 92189389-G-T

40980913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: synonymous variant
orthologous variants: 92189493-T-C

40981060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: synonymous variant
orthologous variants: 92189640-A-G

40981085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92189664-G-A

http://identifiers.org/hco/12/GRCh38#40991853-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92191418-A-C

40991859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92191424-G-A

40991954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92191530-A-G

40991997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92191571-G-T

40992000-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92191574-T-A

http://identifiers.org/hco/12/GRCh38#40992139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92191702-C-A

40992139-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92191702-C-G

40992187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92191748-T-C

40992280-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92191809-T-A

40992286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92191815-C-T

40992471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92192042-G-A

40992471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92192042-G-T

40992485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92192056-C-T

40992697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92192228-C-T

http://identifiers.org/hco/12/GRCh38#40993020-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92192788-A-C

http://identifiers.org/hco/12/GRCh38#40993032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92192799-C-A

http://identifiers.org/hco/12/GRCh38#40993114-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92192863-A-C

40993114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 92192863-A-G

40993142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: synonymous variant
orthologous variants: 92192891-T-C

40993166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: synonymous variant
orthologous variants: 92192915-C-T

40993307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92193052-T-C

http://identifiers.org/hco/12/GRCh38#40993321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92193064-C-A

40993321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92193064-C-T

40993485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92193228-T-C

http://identifiers.org/hco/12/GRCh38#40993496-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92193239-A-C

40993681-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92193416-C-G

40994037-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92195063-C-G

40994037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92195063-C-T

40994050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92195055-T-C

40994081-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92195024-A-T

40994096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92195009-A-G

40994214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92194902-C-T

40994361-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92194769-G-C

40994706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92194432-T-C

40994734-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92194399-T-G

40994972-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92194164-G-C

40995026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92194117-G-A

40995125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92194071-A-G

40995244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92193913-G-T

40995257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92193900-G-A

40997063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92195766-C-T

40997149-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92195852-T-G

40999037-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92197914-G-C

40999191-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92198063-A-T

40999407-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92198256-C-G

40999579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92198421-T-C

41000165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92198667-G-A

41000192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92198692-T-C

41000249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92198749-G-A

41000255-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92198755-C-G

41000259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92198759-A-G

41000332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92198833-G-A

41006587-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92199325-A-T

41006593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92199331-A-G

41006801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92199546-G-T

41006809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92199554-G-T

41006822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92199567-A-G

41014122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92200743-G-A

41014122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92200743-G-T

41014177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92200806-G-T

41014429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92201031-T-C

41014720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92201307-G-A

http://identifiers.org/hco/12/GRCh38#41014781-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#92201346-A-C

41014781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92201346-A-G

41014872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92201410-A-G

41014953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92201486-A-G

41015889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92202195-C-T

41015930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92202237-T-C

41015987-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92202292-C-G

41016011-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92202318-T-G

41016035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92202341-G-A

41016035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92202341-G-T

41016130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92202413-T-C

41016130-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92202413-T-G

http://identifiers.org/hco/12/GRCh38#41016184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92202466-C-A

41016184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92202466-C-T

41016185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92202467-G-A

41016185-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92202467-G-C

41016185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92202467-G-T

41016255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92202538-A-G

41016315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92202596-G-A

41016461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92202706-G-A

41016507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92202737-A-G

41016526-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92202756-G-C

http://identifiers.org/hco/12/GRCh38#41016658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92202886-C-A

41016658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92202886-C-T

41016675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 92202903-T-C

41016705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 92202933-T-C

41016935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92203163-T-C

http://identifiers.org/hco/12/GRCh38#41017005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92203220-C-A

41017152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92203377-C-T

41017191-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92203410-C-G

41017252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92203468-A-G

41018219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92205676-G-A

41018440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92206007-T-C

41019198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92206226-C-T

41019233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92206267-A-G

41019342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92206391-A-G

41019713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92206757-T-C

41019731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92206774-G-A

41019767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92206811-T-C

41019847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92206884-G-A

41019847-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92206884-G-C

41020200-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92207701-T-A

41020230-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92207738-T-G

41020515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92208032-G-A

41020515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92208032-G-T

41020523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92208039-G-A

41020523-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92208039-G-C

http://identifiers.org/hco/12/GRCh38#41020527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92208043-C-A

41020535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92208051-T-C

41020546-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92208062-T-A

41020554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92208070-T-C

http://identifiers.org/hco/12/GRCh38#41020587-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92208103-A-C

41024166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92211285-T-C

41024269-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92211382-T-G

41024478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92211610-T-C

41024557-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92211707-T-G

41024922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92212166-T-C

41025006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92212235-G-A

41025006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92212235-G-T

41025045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92212266-T-C

http://identifiers.org/hco/12/GRCh38#41025078-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92212298-A-C

41025078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92212298-A-G

41025082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92212302-G-T

http://identifiers.org/hco/12/GRCh38#41025084-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92212304-A-C

http://identifiers.org/hco/12/GRCh38#41025133-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92212352-A-C

41025368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92212587-A-G

41025393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92212621-G-T

41025529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92212783-C-T

41025698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92212931-A-G

41025704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92212949-T-C

41025762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92212995-T-C

41025826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92213043-C-T

41025864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92213080-C-T

41025902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92213102-G-A

http://identifiers.org/hco/12/GRCh38#41025904-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92213104-A-C

41025931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92213120-A-G

41026119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92213287-T-C

41026119-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92213287-T-G

41026413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92213613-G-T

41026810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92213983-T-C

41026890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92214030-T-C

41026904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92214044-C-T

41026983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92214125-A-G

41026997-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92214136-G-C

41027632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92214674-A-G

41027657-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92214702-T-G

http://identifiers.org/hco/12/GRCh38#41027663-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92214708-A-C

41027672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92214713-T-C

41027676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92214720-G-A

41027676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92214720-G-T

41027677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92214721-T-C

http://identifiers.org/hco/12/GRCh38#41027749-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92214795-A-C

http://identifiers.org/hco/12/GRCh38#41027844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92214895-C-A

41027844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92214895-C-T

41027888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 92214939-A-G

41028220-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92215040-C-G

41028244-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92215047-G-C

41028298-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92215078-C-G

41028391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92215168-A-G

41028391-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92215168-A-T

41028481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92215259-A-G

41028485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92215263-A-G

41028520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92215298-G-A

41028520-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92215298-G-C

41028834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92215620-C-T

41029021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92215757-A-G

41029037-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: intron variant
orthologous variants: 92215773-A-T

41029197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 92215932-G-A

41029200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 92215935-G-A

41029306-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92216015-T-G

41029321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92216038-A-G

41029357-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92216073-T-A

41029357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92216073-T-C

41029372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92216088-C-T

41029638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92216228-C-T

41029914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92216473-T-C

http://identifiers.org/hco/12/GRCh38#41030152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92216621-C-A

41030327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92216743-C-T

41030359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92216775-T-C

41030452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92216865-A-G

http://identifiers.org/hco/12/GRCh38#41030499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92216911-C-A

41030499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92216911-C-T

41030520-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92216925-A-T

41030691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92217161-C-T

41030745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92217225-A-G

41030809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92217280-A-G

41030833-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92217303-A-T

http://identifiers.org/hco/12/GRCh38#41031246-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92217716-A-C

41031246-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92217716-A-T

41031360-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92217811-T-A

http://identifiers.org/hco/12/GRCh38#41031502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92217960-C-A

41031621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92218079-G-A

41031802-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92218244-C-G

41031822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92218264-C-T

41031885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92218330-G-A

41032026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92218452-G-A

41032026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92218452-G-T

41034898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92219020-G-A

41034898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92219020-G-T

41034928-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92219052-G-C

41034969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92219070-A-G

41035168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92219261-T-C

41035185-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92219278-G-C

http://identifiers.org/hco/12/GRCh38#41035186-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92219279-A-C

41035263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92219356-G-A

41035329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92219439-A-G

41035396-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92219489-C-G

http://identifiers.org/hco/12/GRCh38#41035402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92219495-C-A

41035402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92219495-C-T

41035448-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92219537-C-G

41035475-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92219564-G-C

41039465-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92220034-A-T

41039547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92220115-A-G

41039551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92220119-G-A

41039609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92220164-G-A

41039621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92220176-G-A

41039633-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92220187-A-T

41039687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92220222-T-C

41039814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92220341-A-G

41039872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92220386-A-G

41039876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92220390-T-C

41040012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92220510-C-T

41040052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92220536-G-A

41040071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92220550-G-A

41040177-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92220589-C-G

41040368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92220790-G-T

41044306-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92221206-A-T

41044674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92221492-A-G

41044702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92221520-T-C

http://identifiers.org/hco/12/GRCh38#41044747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92221550-C-A

41044756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92221559-A-G

41045936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92221814-G-A

41045939-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92221817-C-G

41045984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92221860-C-T

41046014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92221866-C-T

41046086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92221930-T-C

41046188-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92222023-C-G

41046205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92222036-T-C

41046235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92222064-G-T

41046293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92222113-A-G

41046297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92222117-T-C

41058327-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92223075-T-G

41058373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: -T-C

41059299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92223603-T-C

41059444-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92223750-A-T

41060370-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92224913-T-G

41060409-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92224951-G-C

41060471-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92225018-G-C

41060599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92225122-G-A

41060599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92225122-G-T

http://identifiers.org/hco/12/GRCh38#41060743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92225258-C-A

41060743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92225258-C-T

41060795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92225307-C-T

41060821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92225332-G-T

41060847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92225358-G-A

41060862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92225373-C-T

41060989-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92225515-C-G

41061071-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92225583-T-G

41061341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92225806-A-G

41061431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92225884-C-T

41061501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92225948-G-A

41061582-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92226041-T-A

41061637-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92226096-T-A

41061703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92226160-G-T

41061708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92226165-A-G

41061711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92226168-G-T

http://identifiers.org/hco/12/GRCh38#41061746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92226203-C-A

41062092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92226517-A-G

41062140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92226565-A-G

41062239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92226667-C-T

41064252-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92227582-A-T

41064326-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92227667-T-A

41064390-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92227727-A-T

41064457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92227809-T-C

41064487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92227839-G-A

41064577-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92227923-A-T

41064587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92227933-C-T

http://identifiers.org/hco/12/GRCh38#41064597-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92227942-A-C

41064973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92228368-G-A

41064986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92228383-G-A

41064989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92228386-A-G

41065001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92228398-T-C

41066931-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92230917-T-G

41066952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92230937-A-G

41066952-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92230937-A-T

41067224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92231215-C-T

41067304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92231305-A-G

41067921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92231607-G-A

http://identifiers.org/hco/12/GRCh38#41068804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92235555-C-A

41069314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92236475-G-A

41069314-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92236475-G-C

41069314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92236475-G-T

41069365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92236526-T-C

http://identifiers.org/hco/12/GRCh38#41069721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92237156-C-A

41069879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92237315-G-A

41069879-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92237315-G-T

41069887-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92237322-T-A

41069887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92237322-T-C

41069887-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 92237322-T-G

41069990-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 92237425-C-G

http://identifiers.org/hco/12/GRCh38#41070068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92237501-C-A

41070068-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 92237501-C-G

41070089-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 92237521-C-G

41070089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 92237521-C-T

http://identifiers.org/hco/12/GRCh38#41070135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92237567-C-A

41070135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 92237567-C-T

41070235-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 92237665-A-T

41070311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: 3 prime UTR variant
orthologous variants: 92237742-T-C

41070352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: 3 prime UTR variant
orthologous variants: 92237782-A-G

41070438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: 3 prime UTR variant
orthologous variants: 92237862-T-C

41070450-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: 3 prime UTR variant
orthologous variants: 92237874-G-T

41070726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: 3 prime UTR variant
orthologous variants: 92238183-G-T

41070783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: 3 prime UTR variant
orthologous variants: 92238250-T-C

41070890-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: 3 prime UTR variant
orthologous variants: 92238357-T-G

41070906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: 3 prime UTR variant
orthologous variants: 92238373-G-T

41070912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: 3 prime UTR variant
orthologous variants: 92238379-T-C

41070928-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: 3 prime UTR variant
orthologous variants: 92238395-G-C

41070928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: 3 prime UTR variant
orthologous variants: 92238395-G-T

41071193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: 3 prime UTR variant
orthologous variants: 92238640-G-A

http://identifiers.org/hco/12/GRCh38#41072163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2171
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92239583-C-A