206939543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: 5 prime UTR variant
orthologous variants: 63943220-G-A

206939543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: 5 prime UTR variant
orthologous variants: 63943220-G-T

http://identifiers.org/hco/2/GRCh38#206939560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63943236-C-A

206939560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: 5 prime UTR variant
orthologous variants: 63943236-C-T

206939605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: missense variant
orthologous variants: 63943285-G-T

206939612-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: missense variant
orthologous variants: 63943292-C-G

206939670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63943343-G-T

206939740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63943415-A-G

206939753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63943428-G-A

206939753-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63943428-G-C

206939753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63943428-G-T

http://identifiers.org/hco/2/GRCh38#206939773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63943448-C-A

206939773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63943448-C-T

206939830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63943505-A-G

206939920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63943564-C-T

206940411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63944039-T-C

206940412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63944040-G-A

206940776-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63944408-T-G

206940848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63944470-A-G

206940864-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63944487-T-G

206940936-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63944565-T-G

206941935-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63948450-T-G

206942286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63948804-G-A

206942381-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63948895-C-G

http://identifiers.org/hco/2/GRCh38#206942677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63949180-C-A

206942848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63949332-G-A

206943423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63950338-A-G

206943802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63950526-C-T

206944195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63950873-G-A

206944456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63951143-G-T

206944554-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63951232-T-A

http://identifiers.org/hco/2/GRCh38#206944603-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63951287-A-C

206945003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63951980-G-A

206945511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63952452-T-C

206945582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63952519-T-C

206945706-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63952623-T-A

206945706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63952623-T-C

206945828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63952683-C-T

206946172-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63952874-T-A

206946381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63953075-A-G

206946452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63953140-G-A

206946567-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63953241-T-A

206946753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63953427-T-C

206946812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63953473-T-C

206947000-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63953628-G-C

206947021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63953649-C-T

206947035-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63953663-T-A

206947579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63954999-C-T

206947651-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63955067-T-A

206947661-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63955077-G-C

206947815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63955213-G-A

206947988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63955351-T-C

http://identifiers.org/hco/2/GRCh38#206948100-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63955465-A-C

206948212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63955570-T-C

206948838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63956162-A-G

206949163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63956318-C-T

http://identifiers.org/hco/2/GRCh38#206949244-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63956399-A-C

206949244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63956399-A-G

http://identifiers.org/hco/2/GRCh38#206949554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63956927-C-A

206949554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63956927-C-T

206949570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63956956-A-G

206949570-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63956956-A-T

206949595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63956981-T-C

206949666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: missense variant
orthologous variants: 63957040-T-C

206949670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: missense variant
orthologous variants: 63957044-G-A

206949711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 63957084-G-A

206949735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63957108-G-A

206949769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63957149-G-T

206949977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63957352-T-C

206949993-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63957368-C-G

206951939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63958596-A-G

206952006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63958627-G-A

206952006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63958627-G-T

206952421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63958720-A-G

http://identifiers.org/hco/2/GRCh38#206952773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63959058-C-A

206952773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63959058-C-T

206955146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63959527-G-A

206955146-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63959527-G-C

206955169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63959550-G-A

206955182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63959557-T-C

http://identifiers.org/hco/2/GRCh38#206955240-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63959618-A-C

206955312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63959691-G-T

http://identifiers.org/hco/2/GRCh38#206955388-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63959770-A-C

http://identifiers.org/hco/2/GRCh38#206955498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: stop gained
orthologous variants: http://identifiers.org/mco/1/GRCm39#63959878-C-A

206955536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: missense variant
orthologous variants: 63959916-A-G

206955586-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63959966-T-G

http://identifiers.org/hco/2/GRCh38#206955701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63960075-C-A

206955701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63960075-C-T

206956894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63961897-A-G

206956910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63961913-C-T

206956934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63961937-G-A

http://identifiers.org/hco/2/GRCh38#206957057-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63962045-A-C

206957063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63962051-G-A

http://identifiers.org/hco/2/GRCh38#206957408-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63962093-A-C

206957489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63962174-C-T

206957519-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63962203-C-G

206957580-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63962261-G-T

206957620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63962301-C-T

206957686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63962366-C-T

206957705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63962382-G-A

206958044-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63962844-T-A

206958219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63963016-G-T

206958256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63963053-A-G

206958279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63963072-G-A

206958279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63963072-G-T

206958327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: missense variant
orthologous variants: 63963120-G-T

206958346-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: missense variant
orthologous variants: 63963137-T-A

206958369-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: missense variant
orthologous variants: 63963151-G-C

206958369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: missense variant
orthologous variants: 63963151-G-T

206958379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: missense variant
orthologous variants: 63963161-G-A

http://identifiers.org/hco/2/GRCh38#206958380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63963162-C-A

http://identifiers.org/hco/2/GRCh38#206958439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63963293-C-A

http://identifiers.org/hco/2/GRCh38#206958443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63963299-C-A

206958447-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63963303-T-A

206958447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63963303-T-C

206958452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63963308-T-C

206958452-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63963308-T-G

206958458-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63963314-T-A

http://identifiers.org/hco/2/GRCh38#206958459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63963391-C-A

206958459-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63963391-C-G

206958493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63963424-A-G

http://identifiers.org/hco/2/GRCh38#206958531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63963450-C-A

206959178-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63963762-G-C

206959351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63963903-C-T

206959371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63963931-C-T

206959500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63964184-A-G

206959509-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63964193-T-G

206959547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63964201-C-T

206959556-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63964210-A-T

http://identifiers.org/hco/2/GRCh38#206959643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63964300-C-A

206959643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: missense variant
orthologous variants: 63964300-C-T

http://identifiers.org/hco/2/GRCh38#206959682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63964350-C-A

206959683-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: missense variant
orthologous variants: 63964351-T-A

206959683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: missense variant
orthologous variants: 63964351-T-C

206959683-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: missense variant
orthologous variants: 63964351-T-G

206959692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: missense variant
orthologous variants: 63964360-A-G

206959692-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: missense variant
orthologous variants: 63964360-A-T

206959705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: synonymous variant
orthologous variants: 63964362-T-C

http://identifiers.org/hco/2/GRCh38#206959729-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: stop gained
orthologous variants: http://identifiers.org/mco/1/GRCm39#63964386-C-A

206959729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: synonymous variant
orthologous variants: 63964386-C-T

206959735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: stop gained
orthologous variants: 63964392-G-A

206959735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: missense variant
orthologous variants: 63964392-G-T

206959753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63964410-A-G

206959757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63964414-T-C

206959774-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63964435-T-G

http://identifiers.org/hco/2/GRCh38#206959807-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63964467-C-A

206959807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63964467-C-T

206959993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63964649-C-T

206960013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63964668-G-A

http://identifiers.org/hco/2/GRCh38#206960201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63964852-C-A

206960395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63965101-T-C

206960456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63965194-C-T

206960660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63965385-G-A

http://identifiers.org/hco/2/GRCh38#206960788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63965608-C-A

206960788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63965608-C-T

206960933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: missense variant
orthologous variants: 63965725-T-C

206960940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 63965732-G-A

206960956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63965748-T-C

206961011-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63965925-T-A

206961014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63965928-A-G

http://identifiers.org/hco/2/GRCh38#206961068-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63965971-A-C

206961068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63965971-A-G

206961080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63965983-C-T

http://identifiers.org/hco/2/GRCh38#206961289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63967303-C-A

http://identifiers.org/hco/2/GRCh38#206962283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63967703-C-A

http://identifiers.org/hco/2/GRCh38#206962315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63967727-C-A

206962315-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63967727-C-G

http://identifiers.org/hco/2/GRCh38#206962320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63967732-C-A

http://identifiers.org/hco/2/GRCh38#206962330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63967736-C-A

206962336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63967742-A-G

http://identifiers.org/hco/2/GRCh38#206962346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63967755-C-A

206962346-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63967755-C-G

206962451-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron_variant, missense_variant
orthologous variants: 63967844-G-C

206962516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron_variant, missense_variant
orthologous variants: 63967973-G-A

206962520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron_variant, missense_variant
orthologous variants: 63967977-A-G

206962524-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron_variant, missense_variant
orthologous variants: 63968070-T-G

http://identifiers.org/hco/2/GRCh38#206962544-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63968090-A-C

206962544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron_variant, missense_variant
orthologous variants: 63968090-A-G

206962786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63968338-C-T

206963362-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63968904-A-T

206963389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63968935-T-C

206963636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63969145-C-T

http://identifiers.org/hco/2/GRCh38#206963990-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63969559-A-C

206963990-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63969559-A-T

206964074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63969635-C-T

206964420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63969968-T-C

206964473-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63970021-C-G

206964473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63970021-C-T

206964545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63970088-C-T

206964691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63970231-A-G

206964920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63970469-A-G

206964985-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63970521-A-T

206965013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63970544-G-A

206965179-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63970659-C-G

206965179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63970659-C-T

206965198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63970678-G-A

206965658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63970934-G-A

206965731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63970995-G-T

206965820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63971083-C-T

206965843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63971104-G-A

206965867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63971125-G-A

http://identifiers.org/hco/2/GRCh38#206965929-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63971221-A-C

206966214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63971598-T-C

206966214-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63971598-T-G

206966490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63971911-A-G

206966586-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63972014-T-G

206966598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63972037-C-T

206967147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63972795-C-T

206967150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63972805-A-G

206967197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63972849-G-A

206967197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63972849-G-T

206967207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63972862-A-G

206967217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63972872-T-C

206967322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63972979-T-C

206967348-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63973000-T-G

206967356-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63973008-T-G

206967482-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63973120-C-G

206967505-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63973142-C-G

206967603-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63973226-T-G

206967700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63973302-G-A

206967726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63973328-T-C

206967899-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63973495-G-C

206967924-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63973522-G-T

206968065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63973669-T-C

206968096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63973700-T-C

http://identifiers.org/hco/2/GRCh38#206968232-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63973836-A-C

206968232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63973836-A-G

http://identifiers.org/hco/2/GRCh38#206968469-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63974079-A-C

206968695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63974304-G-A

206968729-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63974350-C-G

206968832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63974528-A-G

206968993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63974685-C-T

http://identifiers.org/hco/2/GRCh38#206969102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#63974771-C-A

206969102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron variant
orthologous variants: 63974771-C-T

206969169-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 63974838-T-G

206969222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 63974889-C-T

206969229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 63974896-A-G

206969229-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 63974896-A-T

206969264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 63974931-G-A

206969264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 63974931-G-T

206969288-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 63974943-T-A

206969433-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 63975088-C-G

206969452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21011
most severe consequence: 3 prime UTR variant
orthologous variants: 63975107-G-A