24172035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: 3 prime UTR variant
orthologous variants: 25391801-T-C

24172335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: 3 prime UTR variant
orthologous variants: 25391565-G-A

24172412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: 3 prime UTR variant
orthologous variants: 25391491-A-G

24172467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: 3 prime UTR variant
orthologous variants: 25391436-G-A

24172520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: 3 prime UTR variant
orthologous variants: 25391388-G-A

24172520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: 3 prime UTR variant
orthologous variants: 25391388-G-T

24173040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: 3 prime UTR variant
orthologous variants: 25391224-G-A

24173040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: 3 prime UTR variant
orthologous variants: 25391224-G-T

24173075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: 3 prime UTR variant
orthologous variants: 25391190-G-A

24173075-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: 3 prime UTR variant
orthologous variants: 25391190-G-C

24173186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: 3 prime UTR variant
orthologous variants: 25391109-C-T

24173349-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: 3 prime UTR variant
orthologous variants: 25390939-G-C

24173501-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: 3 prime UTR variant
orthologous variants: 25390795-T-A

24173511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: 3 prime UTR variant
orthologous variants: 25390785-G-A

24173670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: 3 prime UTR variant
orthologous variants: 25390572-T-C

24173775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: 3 prime UTR variant
orthologous variants: 25390396-A-G

24173917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: 3 prime UTR variant
orthologous variants: 25390249-A-G

24173917-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: 3 prime UTR variant
orthologous variants: 25390249-A-T

24173958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: 3 prime UTR variant
orthologous variants: 25390200-G-A

24173958-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: 3 prime UTR variant
orthologous variants: 25390200-G-C

http://identifiers.org/hco/6/GRCh38#24174029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25390168-C-A

24174029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: 3 prime UTR variant
orthologous variants: 25390168-C-T

24174048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: 3 prime UTR variant
orthologous variants: 25390149-T-C

24174184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: 3 prime UTR variant
orthologous variants: 25390044-A-G

24174191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: 3 prime UTR variant
orthologous variants: 25390037-G-A

24174191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: 3 prime UTR variant
orthologous variants: 25390037-G-T

http://identifiers.org/hco/6/GRCh38#24174220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25390014-C-A

24174220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: 3 prime UTR variant
orthologous variants: 25390014-C-T

24174268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: 3 prime UTR variant
orthologous variants: 25389968-T-C

http://identifiers.org/hco/6/GRCh38#24174330-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25389906-A-C

24174330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: 3 prime UTR variant
orthologous variants: 25389906-A-G

24174455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: 3 prime UTR variant
orthologous variants: 25389770-A-G

24174516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: 3 prime UTR variant
orthologous variants: 25389704-G-T

24174562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: 3 prime UTR variant
orthologous variants: 25389658-G-T

http://identifiers.org/hco/6/GRCh38#24174631-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25389595-A-C

24174631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: 3 prime UTR variant
orthologous variants: 25389595-A-G

24174631-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: 3 prime UTR variant
orthologous variants: 25389595-A-T

24174707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: 3 prime UTR variant
orthologous variants: 25389521-T-C

24174737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: missense variant
orthologous variants: 25389492-A-G

24174761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: missense variant
orthologous variants: 25389468-T-C

24174785-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: missense variant
orthologous variants: 25389444-C-G

24174858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25389370-A-G

http://identifiers.org/hco/6/GRCh38#24174859-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25389369-A-C

24174859-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25389369-A-T

24175254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25388831-T-C

24175496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25388600-G-A

24175589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25388489-G-A

24175589-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25388489-G-C

24177183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25387221-G-A

24177250-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25387153-G-C

24177250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25387153-G-T

24177306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25387094-A-G

24177856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25386939-A-G

24178086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25386721-A-G

24178159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25386638-A-G

24178163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25386634-T-C

http://identifiers.org/hco/6/GRCh38#24178243-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25386568-A-C

http://identifiers.org/hco/6/GRCh38#24178302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25386475-C-A

24178302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25386475-C-T

24178370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: missense variant
orthologous variants: 25386408-T-C

http://identifiers.org/hco/6/GRCh38#24178381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25386397-C-A

24178459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: synonymous variant
orthologous variants: 25386319-T-C

24178504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: synonymous variant
orthologous variants: 25386274-G-A

http://identifiers.org/hco/6/GRCh38#24178600-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25386178-A-C

24178859-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25385943-T-A

24178912-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25385883-A-T

http://identifiers.org/hco/6/GRCh38#24178969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25385832-C-A

24179083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25385719-A-G

24179092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25385710-A-G

24181142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25385375-C-T

24181362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25385247-C-T

24181451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25385151-G-A

24181630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25384868-G-A

24183992-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25384705-C-G

24183995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25384701-A-G

24184077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25384626-G-A

24184202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25384489-G-A

24184937-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25383979-A-T

24185226-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25383733-T-A

http://identifiers.org/hco/6/GRCh38#24185285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25383675-C-A

24185285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25383675-C-T

24185348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25383613-G-A

24185466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25383495-C-T

http://identifiers.org/hco/6/GRCh38#24186937-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25381156-A-C

24187328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25380813-G-T

24187331-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25380810-A-T

24187413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25380732-C-T

24187595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25380553-C-T

24187781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25380384-G-T

24188119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25380151-G-A

24188119-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25380151-G-C

24188191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25380086-T-C

24188595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25379803-T-C

24188684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25379716-T-C

24188868-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25379552-G-C

24189730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25378949-A-G

24189925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25378748-G-A

24190611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25378357-T-C

24190630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25378338-A-G

24190809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25378159-T-C

24190920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25378048-T-C

24191383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25377635-G-A

24191399-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25377628-C-G

24191399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25377628-C-T

24191451-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25377577-C-G

24191501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25377525-A-G

24191569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25377470-A-G

24191618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25377424-G-A

24196820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25374023-A-G

24196839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25374004-G-A

24196982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25373872-G-A

24197044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25373805-A-G

24198178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25372089-G-A

24198178-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25372089-G-T

24198201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25372066-A-G

24204933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25371812-G-T

http://identifiers.org/hco/6/GRCh38#24205114-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25371645-A-C

24205119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 25371640-A-G

24205146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 25371606-C-T

24205189-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron_variant, missense_variant
orthologous variants: 25371566-T-G

24205201-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron_variant, missense_variant
orthologous variants: 25371554-T-G

24205203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 25371552-G-A

24205203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 25371552-G-T

http://identifiers.org/hco/6/GRCh38#24205245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25371522-C-A

24205378-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25371420-T-A

24205378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25371420-T-C

24205378-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25371420-T-G

24205380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25371418-G-T

24206145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25370717-T-C

http://identifiers.org/hco/6/GRCh38#24210927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25367138-C-A

24210927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25367138-C-T

24210949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25367116-C-T

24210960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25367105-T-C

24211599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25366511-G-T

http://identifiers.org/hco/6/GRCh38#24211796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25366359-C-A

24211829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25366326-G-A

http://identifiers.org/hco/6/GRCh38#24212305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25366224-C-A

24212372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25366150-T-C

24212386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25366136-T-C

24212682-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25365860-C-G

24212829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25365713-A-G

24212908-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25365635-A-T

24213242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25365010-G-A

24213494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25364719-T-C

24214383-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25363801-T-G

24214480-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25363702-T-A

24214480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25363702-T-C

24214480-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25363702-T-G

24214579-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25363591-T-A

24214875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25363313-T-C

24214928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25363269-C-T

24215341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25362898-G-A

24215534-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25362701-G-T

24215590-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25362657-A-T

24215763-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25362447-C-G

24215763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25362447-C-T

24215803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25362403-C-T

24216521-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25357019-G-C

24216857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25356658-A-G

24216987-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25356529-G-C

24217055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25356489-A-G

24217056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25356488-T-C

24217486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25355502-G-A

http://identifiers.org/hco/6/GRCh38#24217535-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25355457-A-C

http://identifiers.org/hco/6/GRCh38#24217764-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25355268-A-C

24217785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25355250-T-C

24219061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25354544-T-C

24219061-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25354544-T-G

24219122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25354490-T-C

24219127-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25354485-T-G

24219376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25354200-G-T

24222006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25353352-G-A

24222193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25353166-G-A

http://identifiers.org/hco/6/GRCh38#24222261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25353101-C-A

24222430-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25352750-T-A

24222566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25352604-T-C

24222620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25352514-A-G

24222684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25352454-A-G

24223363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25351785-A-G

http://identifiers.org/hco/6/GRCh38#24223379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25351775-C-A

24223379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25351775-C-T

24223443-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25351713-T-A

http://identifiers.org/hco/6/GRCh38#24223779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25351379-C-A

24223913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25351256-G-A

24223913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25351256-G-T

24224545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25349986-A-G

24224987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25348578-G-A

http://identifiers.org/hco/6/GRCh38#24225695-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25347807-A-C

24225695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25347807-A-G

24226965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25345874-T-C

24226985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25345852-G-A

http://identifiers.org/hco/6/GRCh38#24227119-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25345744-A-C

http://identifiers.org/hco/6/GRCh38#24227120-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25345743-A-C

24227129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25345735-G-T

http://identifiers.org/hco/6/GRCh38#24227152-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25345712-A-C

24227432-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25345436-C-G

24227432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25345436-C-T

24227528-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25345358-C-G

24227702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25345201-G-A

24227968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25345069-C-T

24228105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25344991-G-A

24228609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25344500-A-G

24228634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25344475-C-T

24228798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25344344-T-C

24229238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25343974-C-T

24229481-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25343748-G-C

24229482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25343746-C-T

24229483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25343745-C-T

24229854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25342601-T-C

http://identifiers.org/hco/6/GRCh38#24229877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25342580-C-A

24231178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25341251-G-A

24231331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25341101-C-T

24231339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25341093-T-C

24231424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25341033-G-A

24231556-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25340907-C-G

http://identifiers.org/hco/6/GRCh38#24231566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25340897-C-A

24231566-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25340897-C-G

24231638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25340828-C-T

24231836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25340646-G-A

24232242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25340278-G-A

24232338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25340173-G-A

24232464-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25340063-T-A

24232583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25339946-T-C

24232766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25339787-G-A

24233116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25339471-C-T

24233776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25338938-T-C

24233783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25338931-T-C

http://identifiers.org/hco/6/GRCh38#24233794-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25338908-A-C

24233794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25338908-A-G

24233819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25338884-T-C

24233924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25338685-C-T

24234022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25338587-A-G

24234028-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25338581-A-T

24234365-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25338297-G-C

24234465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25338198-G-A

24234512-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25338159-T-G

24234764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25337919-G-A

24234764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25337919-G-T

http://identifiers.org/hco/6/GRCh38#24234892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25337744-C-A

24238848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25336968-G-A

24238931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25336889-C-T

24239091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25336734-A-G

24239284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25336575-A-G

24239437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25336328-A-G

24239674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25335691-G-A

24239674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25335691-G-T

24239675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25335690-C-T

http://identifiers.org/hco/6/GRCh38#24239697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25335668-C-A

24239714-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25335651-C-G

24239748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25335612-A-G

24239986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25335287-G-A

24240308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25334983-G-A

24240364-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25334926-G-C

http://identifiers.org/hco/6/GRCh38#24240529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25334759-C-A

24240648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25334639-G-A

24240648-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25334639-G-C

24241285-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25332722-A-T

24241311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25332695-T-C

24241408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25332601-C-T

24241834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25332150-C-T

http://identifiers.org/hco/6/GRCh38#24244316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25331249-C-A

24244316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25331249-C-T

http://identifiers.org/hco/6/GRCh38#24244619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25330972-C-A

24244619-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25330972-C-G

http://identifiers.org/hco/6/GRCh38#24247371-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25329253-A-C

24247458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25329172-T-C

24247514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25329125-T-C

24248714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25327679-T-C

24248714-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25327679-T-G

24248841-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25327556-T-A

24248932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25327462-A-G

http://identifiers.org/hco/6/GRCh38#24249327-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25326832-A-C

http://identifiers.org/hco/6/GRCh38#24249365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25326808-C-A

24250187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25326060-C-T

24250211-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25326036-T-A

24250345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25325941-G-A

24250359-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25325927-C-G

24250493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25325789-T-C

24250655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25325653-G-T

24250656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25325652-C-T

24256374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25322340-A-G

24256381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25322333-A-G

24256519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25322222-C-T

24256733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25321981-T-C

24257320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25321426-T-C

24257548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25321137-T-C

24257715-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25321004-T-A

24257715-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25321004-T-G

http://identifiers.org/hco/6/GRCh38#24257724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25320995-C-A

24257724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25320995-C-T

24257818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25320907-A-G

24257844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25320881-G-A

24257844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25320881-G-T

http://identifiers.org/hco/6/GRCh38#24259510-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25318980-A-C

24259742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25318753-A-G

24259759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25318738-T-C

24260206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25318486-A-G

24260480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25318076-C-T

24260640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25317892-T-C

24260664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25317867-G-T

http://identifiers.org/hco/6/GRCh38#24260838-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25317704-A-C

24260838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25317704-A-G

24261008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25317534-A-G

24261015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25317527-G-A

24261015-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25317527-G-C

24261102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25317442-G-A

24261102-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25317442-G-C

24268945-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25312155-T-A

24268945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25312155-T-C

24269241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25311856-A-G

24269426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25311665-G-T

24269551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25311541-G-T

24269553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25311539-G-A

24269567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25311511-G-A

24269622-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25311462-G-T

http://identifiers.org/hco/6/GRCh38#24269638-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25311448-A-C

24270168-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25310869-T-G

24270175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25310862-C-T

24270184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25310853-C-T

24270186-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25310851-G-C

http://identifiers.org/hco/6/GRCh38#24270233-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25310603-A-C

24271669-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25310331-C-G

24271697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25310304-C-T

24271712-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25310289-T-G

24271988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25308392-A-G

24272092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25308325-T-C

24272135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25308224-A-G

24272194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25308172-A-G

24273563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25307867-G-A

24273568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25307862-C-T

24273636-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron_variant, undefined
orthologous variants: 25307803-T-A

24273636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron_variant, undefined
orthologous variants: 25307803-T-C

24273688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron_variant, undefined
orthologous variants: 25307754-G-A

24273820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25307625-A-G

24274111-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25307371-C-G

24274111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25307371-C-T

24274306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25307216-A-G

24274380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25307143-G-A

24274415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25307115-T-C

24274418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25307112-G-A

24274461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25307077-A-G

24274567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25306972-G-A

24274567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25306972-G-T

24274696-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25306876-T-G

24274863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25306733-A-G

24275221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25306396-A-G

24275236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25306381-A-G

24275327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25306308-T-C

24275412-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25306226-C-G

24275614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25306001-G-A

24275629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25305985-T-C

24275734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25305882-G-T

24276581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25305265-T-C

24276598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25305244-G-T

http://identifiers.org/hco/6/GRCh38#24276606-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25305236-A-C

24276651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25305190-T-C

24276741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25305101-C-T

http://identifiers.org/hco/6/GRCh38#24276869-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25304975-A-C

24276958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25304894-C-T

http://identifiers.org/hco/6/GRCh38#24277004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25304856-C-A

24277195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25304574-G-A

24277195-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25304574-G-C

24277405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25304313-C-T

24277659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25303967-T-C

24277778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25303844-G-A

24278011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25303458-A-G

24278168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: missense variant
orthologous variants: 25303271-T-C

24278168-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: missense variant
orthologous variants: 25303271-T-G

24278223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25303216-A-G

24278223-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25303216-A-T

http://identifiers.org/hco/6/GRCh38#24278361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25303092-C-A

24278361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25303092-C-T

24278380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25303073-G-A

24280139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25302412-A-G

http://identifiers.org/hco/6/GRCh38#24280850-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25302044-A-C

24282840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25300435-G-A

24283118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron_variant, undefined
orthologous variants: 25300170-G-A

24283118-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron_variant, undefined
orthologous variants: 25300170-G-C

24283118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron_variant, undefined
orthologous variants: 25300170-G-T

24283140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25300148-A-G

24283143-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25300145-A-T

24283194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron_variant, undefined
orthologous variants: 25300099-T-C

24283223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25300082-A-G

24283382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron_variant, undefined
orthologous variants: 25299946-A-G

24283472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25299861-C-T

24283535-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25299797-A-T

http://identifiers.org/hco/6/GRCh38#24283595-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#25299756-A-C

24283834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron_variant, undefined
orthologous variants: 25299523-G-A

24283850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25299507-C-T

24283858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25299499-G-A

24284048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25299324-C-T

24284049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25299323-G-A

24284076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25299296-G-A

24284195-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25299179-C-G

24285211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25297605-G-A

24285211-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25297605-G-C

24285304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25297511-T-C

24285420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25297403-T-C

24285544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25297276-C-T

24285795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25297048-A-G

24286933-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25296120-C-G

24287344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25295750-G-A

http://identifiers.org/hco/6/GRCh38#24287578-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25295506-A-C

24287578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25295506-A-G

24287632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25295452-C-T

24287688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25295404-C-T

24287701-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25295391-T-G

24287788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25295348-T-C

24287828-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25295308-G-C

http://identifiers.org/hco/6/GRCh38#24287854-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25295290-A-C

24287854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25295290-A-G

24287941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25295220-A-G

24287945-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25295216-G-C

24288142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25295043-A-G

24288205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25294993-A-G

24288381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25294616-T-C

24288382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25294615-A-G

24288382-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25294615-A-T

24288508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25294429-T-C

24288820-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25294134-G-C

24288820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25294134-G-T

24288828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25294126-A-G

24288910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 25294044-T-C

24288910-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 25294044-T-G

24288963-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25293991-T-A

24289274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25293625-C-T

24289422-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25293424-A-T

24289844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25293046-G-A

24289844-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25293046-G-C

24289896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25293000-G-A

24290712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25292099-T-C

24290908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25291745-G-A

http://identifiers.org/hco/6/GRCh38#24291007-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25291643-A-C

24291007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: missense variant
orthologous variants: 25291643-A-G

24291094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25291558-A-G

24291116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25291537-C-T

24291195-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25291498-T-A

24291228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25291465-C-T

24291338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25291378-T-C

24291491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25291316-T-C

24291543-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25291255-T-G

24291635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25291200-G-A

24291796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25291091-T-C

24291954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25290939-A-G

24292359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25290447-T-C

24292470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25290375-T-C

24292814-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25289994-G-C

24292888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25289929-T-C

24293353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25289587-C-T

24297550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25289203-A-G

24297810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25288979-T-C

http://identifiers.org/hco/6/GRCh38#24300438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25287897-C-A

24300497-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25287831-T-G

http://identifiers.org/hco/6/GRCh38#24301397-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25286947-A-C

24301397-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25286947-A-T

24301559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25286788-G-A

http://identifiers.org/hco/6/GRCh38#24301631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25286717-C-A

24301668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25286681-T-C

24301699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25286648-G-A

24301705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25286643-T-C

24301980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: missense variant
orthologous variants: 25286378-G-A

24301989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: missense variant
orthologous variants: 25286369-A-G

24302013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: missense variant
orthologous variants: 25286345-A-G

24302058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25286300-G-A

24302058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25286300-G-T

24305237-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25283371-C-G

24305419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25283180-T-C

24305420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25283179-A-G

24307326-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25281593-G-C

24307492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25281461-T-C

http://identifiers.org/hco/6/GRCh38#24307568-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25281399-A-C

24308068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25280381-T-C

24308165-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25280283-G-C

24308257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25280184-T-C

24308303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25280147-A-G

24308394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25280057-A-G

http://identifiers.org/hco/6/GRCh38#24308601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25279861-C-A

24310017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25279231-A-G

24310088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25279165-C-T

24310481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25278598-C-T

24310509-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25278570-T-A

24310538-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25278541-C-G

24310599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25278458-A-G

24310603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25278454-T-C

24310657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25278360-C-T

http://identifiers.org/hco/6/GRCh38#24310792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25278252-C-A

http://identifiers.org/hco/6/GRCh38#24310979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25278105-C-A

24310979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25278105-C-T

24311016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25278069-C-T

24311134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25277953-G-T

24311226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25277866-T-C

24311386-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25277720-A-T

24311480-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25277581-G-C

24311618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25277460-T-C

24311668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25277404-T-C

24312388-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25276843-A-T

24312596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25276657-T-C

24312877-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25276397-T-G

24313229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron_variant, undefined
orthologous variants: 25275605-C-T

24313426-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron_variant, undefined
orthologous variants: 25275420-A-T

24313444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron_variant, undefined
orthologous variants: 25275407-A-G

24313747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron_variant, undefined
orthologous variants: 25275083-G-A

24314040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25274780-G-A

http://identifiers.org/hco/6/GRCh38#24314055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25274764-C-A

24314694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25274415-C-T

http://identifiers.org/hco/6/GRCh38#24314817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25274272-C-A

24314923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25274120-A-G

24314929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25274111-G-T

24315288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25273117-C-T

24323730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25267677-G-A

24323768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25267642-C-T

24323770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25267640-T-C

24324393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25264247-T-C

24324978-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25264050-G-C

24324978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25264050-G-T

24324983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25264045-C-T

24325054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25263983-C-T

24325215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25263843-C-T

24325391-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25263667-T-A

24329668-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25262858-A-T

http://identifiers.org/hco/6/GRCh38#24330656-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#25261121-A-C

24330656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron_variant, undefined
orthologous variants: 25261121-A-G

24330656-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron_variant, undefined
orthologous variants: 25261121-A-T

24330976-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25260794-T-A

24330976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25260794-T-C

24331169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25260605-T-C

24332781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25259392-A-G

24335314-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25258307-G-C

24335339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25258287-G-A

24337090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25257708-T-C

24341174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron_variant, undefined
orthologous variants: 25254326-T-C

http://identifiers.org/hco/6/GRCh38#24341562-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25253951-A-C

24341618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25253900-A-G

24341733-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25253799-G-C

24344414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25253735-C-T

24344560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25253597-G-A

24344820-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25251662-G-C

24344820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25251662-G-T

24344967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25251516-T-C

24345309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25251238-T-C

24345391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25251155-A-G

24345463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25251084-C-T

24345724-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25250805-C-G

24345724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25250805-C-T

24345764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25250776-G-T

24345767-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25250773-T-A

http://identifiers.org/hco/6/GRCh38#24346285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25250406-C-A

24346285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25250406-C-T

24346345-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25250346-T-A

24346345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25250346-T-C

24346378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25250328-G-A

24348358-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25249878-G-C

http://identifiers.org/hco/6/GRCh38#24348389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25249848-C-A

24348424-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25249817-A-T

24348502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25249743-G-A

24349115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25248869-G-T

24349142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25248844-G-A

24349142-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25248844-G-C

24349258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25248742-A-G

24352612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25247344-G-A

24352708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25247178-T-C

24352739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25247148-C-T

24352772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25247128-T-C

24352801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25247100-A-G

http://identifiers.org/hco/6/GRCh38#24353182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25245655-C-A

http://identifiers.org/hco/6/GRCh38#24353207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25245624-C-A

http://identifiers.org/hco/6/GRCh38#24353280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25245555-C-A

24353280-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 25245555-C-G

24353483-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25245358-G-C

24353483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25245358-G-T

24353496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25245345-A-G

http://identifiers.org/hco/6/GRCh38#24353510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25245333-C-A

24353654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25245188-T-C

24353684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25245155-T-C

http://identifiers.org/hco/6/GRCh38#24353732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25245107-C-A

http://identifiers.org/hco/6/GRCh38#24354005-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25244602-A-C

24354005-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25244602-A-T

http://identifiers.org/hco/6/GRCh38#24354078-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25244529-A-C

24354092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25244515-C-T

24354168-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25244437-C-G

24354170-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25244435-T-A

24354170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25244435-T-C

http://identifiers.org/hco/6/GRCh38#24354267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25244355-C-A

24354268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25244354-G-A

24354334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25244295-G-A

http://identifiers.org/hco/6/GRCh38#24354361-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25244270-A-C

24354448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25244013-A-G

24354497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25243962-C-T

24354553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25243908-C-T

24354583-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25243882-A-T

24355065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25243230-C-T

24355145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25243157-G-A

24355779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25241938-C-T

24355856-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25241868-T-G

24355985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25241771-G-A

24356116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25241640-A-G

24356153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25241618-A-G

24356305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25241484-C-T

24356430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25241388-T-C

24356446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25241369-G-A

24356678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25241188-T-C

24356865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: 25241049-A-G

http://identifiers.org/hco/6/GRCh38#24356896-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#25241030-C-A

24356979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron_variant, undefined
orthologous variants: 25240947-T-C

http://identifiers.org/hco/6/GRCh38#24357227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#25240701-C-A

24357227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron_variant, undefined
orthologous variants: 25240701-C-T

http://identifiers.org/hco/6/GRCh38#24357358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#25240608-C-A

24357373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron_variant, undefined
orthologous variants: 25240599-G-A

24357373-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron_variant, undefined
orthologous variants: 25240599-G-C

24357373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron_variant, undefined
orthologous variants: 25240599-G-T

24357380-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron_variant, undefined
orthologous variants: 25240592-T-A

24357380-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron_variant, undefined
orthologous variants: 25240592-T-G

24357728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: missense_variant, undefined
orthologous variants: 25240274-G-A

24357728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: missense_variant, undefined
orthologous variants: 25240274-G-T

24357824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 25240209-G-A

24357824-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 25240209-G-C

http://identifiers.org/hco/6/GRCh38#24357898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#25240145-C-A

24357898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25240145-C-T

24357955-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25240108-G-C

24357979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25240100-G-A

24357979-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25240100-G-C

http://identifiers.org/hco/6/GRCh38#24358033-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#25240050-C-A

24358033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25240050-C-T

24358079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron_variant, undefined
orthologous variants: 25240012-G-A

24358079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18141
most severe consequence: intron_variant, undefined
orthologous variants: 25240012-G-T