100357090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: 5 prime UTR variant
orthologous variants: 89457072-C-T

100357112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: 5 prime UTR variant
orthologous variants: 89457050-G-A

100357112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: 5 prime UTR variant
orthologous variants: 89457050-G-T

100357205-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: 5 prime UTR variant
orthologous variants: 89456960-G-C

100357205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: 5 prime UTR variant
orthologous variants: 89456960-G-T

100357224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: 5 prime UTR variant
orthologous variants: 89456941-G-A

100357224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: 5 prime UTR variant
orthologous variants: 89456941-G-T

100357316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: 5 prime UTR variant
orthologous variants: 89456847-T-C

100357374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: 5 prime UTR variant
orthologous variants: 89456789-A-G

100357408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: missense variant
orthologous variants: 89456743-T-C

100357461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: missense variant
orthologous variants: 89456690-G-A

100357461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: missense variant
orthologous variants: 89456690-G-T

http://identifiers.org/hco/12/GRCh38#100357578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89456572-C-A

100357578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89456572-C-T

http://identifiers.org/hco/12/GRCh38#100357605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89456545-C-A

100357605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89456545-C-T

100357641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89456510-T-C

100357700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89456382-A-G

100357713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89456369-T-C

100357713-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89456369-T-G

100357826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89456231-G-A

100357995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89456009-A-G

100357995-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89456009-A-T

http://identifiers.org/hco/12/GRCh38#100358012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89455987-C-A

100358079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89455921-G-T

100358122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89455879-T-C

100358271-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89455726-T-A

100358462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89455544-G-A

http://identifiers.org/hco/12/GRCh38#100358721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89455304-C-A

100358721-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89455304-C-G

100358721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89455304-C-T

100359284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89454894-G-A

100359452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89454730-G-A

100359479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89454703-T-C

100359547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89454485-G-A

100360029-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89453753-C-G

100360029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89453753-C-T

100360064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89453718-G-A

100360116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89453676-C-T

100360206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89453587-C-T

100360263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89453528-G-A

100360654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89453300-G-T

100361243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89452575-G-A

100361243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89452575-G-T

100361448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89452392-A-G

100361528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89452292-C-T

100362649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89451914-A-G

100362992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89451578-G-T

100363168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89451410-C-T

100372894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89446234-T-C

100372915-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89446212-T-A

100372915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89446212-T-C

100372991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89446145-G-A

100373001-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89446130-G-C

100373001-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89446130-G-T

100373060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89446073-G-T

100373087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89446046-G-A

100373109-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89446025-C-G

100373272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89445863-T-C

100373453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89445721-T-C

100379556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89444094-A-G

100380497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89442902-C-T

100380562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89442857-G-A

100380584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89442840-C-T

100380711-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: missense variant
orthologous variants: 89442718-G-C

100380767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: synonymous variant
orthologous variants: 89442662-G-A

http://identifiers.org/hco/12/GRCh38#100380782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89442647-C-A

100380782-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: missense variant
orthologous variants: 89442647-C-G

100380782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: synonymous variant
orthologous variants: 89442647-C-T

100380811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: missense variant
orthologous variants: 89442618-G-A

100380849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: synonymous variant
orthologous variants: 89442541-C-T

100381348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89442238-C-T

100381405-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89442176-G-C

100381471-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89442113-T-G

http://identifiers.org/hco/12/GRCh38#100381495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89442085-C-A

100381621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89441972-G-T

100381631-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89441968-C-G

100381636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89441963-G-A

100381846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89441736-G-A

http://identifiers.org/hco/12/GRCh38#100382828-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89441085-A-C

100382904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89441017-G-A

100383017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89440909-G-A

100383032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89440878-G-A

100383119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89440801-G-A

100383128-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89440792-C-G

100383214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89440712-G-T

100383247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89440681-G-T

100383300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89440628-G-A

100383566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89440154-A-G

100383615-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89440109-G-C

100384122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89439817-C-T

100384250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89439709-T-C

100391222-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89435958-C-G

100391268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89435912-G-T

100391749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89435751-T-C

100391804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89435701-C-T

100391859-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89435647-G-C

100392089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89435426-T-C

100392228-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89435290-C-G

100392296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89435222-G-T

100392350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89435166-G-A

http://identifiers.org/hco/12/GRCh38#100393337-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89434643-C-A

100393337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89434643-C-T

100393427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: missense variant
orthologous variants: 89434553-G-A

100393485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: splice donor variant
orthologous variants: 89434495-T-C

100393490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 89434488-G-A

100393499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89434479-C-T

100395973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89433746-T-C

100396182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89433540-T-C

100396442-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89433283-A-T

100397356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89432521-A-G

100397437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89432442-G-A

100398350-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89432126-A-T

100398539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89431955-T-C

http://identifiers.org/hco/12/GRCh38#100398568-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89431926-A-C

100400378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89430486-G-A

http://identifiers.org/hco/12/GRCh38#100400565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89430311-C-A

100400605-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89430272-C-G

http://identifiers.org/hco/12/GRCh38#100400825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89430028-C-A

100400972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89429926-C-T

100401380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89429261-G-A

100401392-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89429252-C-G

100401533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89429113-A-G

100401625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89429020-G-A

100401892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89428707-T-C

100401895-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89428703-G-T

100401896-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89428702-A-T

100402079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89428541-C-T

100402173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 89428230-T-C

100402194-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 89428209-T-G

100402196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 89428207-A-G

http://identifiers.org/hco/12/GRCh38#100402208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89428196-C-A

100402208-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 89428196-C-G

100402208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 89428196-C-T

100402248-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 89428121-A-T

100402267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89428096-G-A

100402348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: missense variant
orthologous variants: 89428013-G-T

100402566-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89427186-T-G

100402692-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 89427059-C-G

100402692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 89427059-C-T

100402769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89426982-A-G

100402789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89426962-T-C

100402789-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89426962-T-G

100402803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89426948-A-G

100402840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89426911-A-G

http://identifiers.org/hco/12/GRCh38#100402958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89426824-C-A

100402989-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89426792-T-G

100403012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89426769-A-G

100403012-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89426769-A-T

100403018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89426763-G-A

100403120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89425994-G-A

100403120-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89425994-G-C

100403668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89425788-A-G

100403862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89425646-G-A

100403862-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89425646-G-C

100403919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89425596-G-T

100403983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89425536-G-A

100403983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89425536-G-T

100404121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 89425405-C-T

100404186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 89425342-T-C

100404313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 89425130-G-T

100404316-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 89425127-T-A

http://identifiers.org/hco/12/GRCh38#100404343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89425100-C-A

100404343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 89425100-C-T

100404354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 89425077-G-T

http://identifiers.org/hco/12/GRCh38#100404361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89424952-C-A

100404361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 89424952-C-T

100404439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron variant
orthologous variants: 89424879-T-C

100411569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89420683-G-A

100411798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89420440-T-C

100411836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89420401-T-C

100411836-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89420401-T-G

100412122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89419650-A-G

100412162-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89419611-T-G

100412264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89419512-A-G

100412296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89419482-A-G

100412722-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89419410-G-C

100412722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89419410-G-T

100412728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89419404-T-C

http://identifiers.org/hco/12/GRCh38#100412739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89419393-C-A

100412739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89419393-C-T

http://identifiers.org/hco/12/GRCh38#100412749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89419387-C-A

100412749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89419387-C-T

100412914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89419222-A-G

100413029-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89419119-G-C

100413029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89419119-G-T

100413418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89418696-A-G

100413457-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89418657-T-A

100413457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89418657-T-C

100413465-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89418649-A-T

100414190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89418277-C-T

100414228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89418247-G-A

100414306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89418167-G-A

100414310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89418160-G-A

100414362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89418117-G-A

100414507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89417985-G-A

100414507-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89417985-G-C

100414577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89417915-C-T

100414873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89417444-G-A

100414965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89417143-G-A

100415083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89417033-C-T

100416207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89416493-T-C

100416282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89416416-C-T

100416565-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89416131-T-A

100416614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89416081-C-T

http://identifiers.org/hco/12/GRCh38#100417949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89413947-C-A

100417949-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89413947-C-G

100417949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89413947-C-T

100418094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 89413823-G-A

100418094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 89413823-G-T

http://identifiers.org/hco/12/GRCh38#100418259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89413662-C-A

100418259-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89413662-C-G

100418360-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89413570-G-C

100418583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89413370-G-T

100419713-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89412601-T-A

100419713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89412601-T-C

http://identifiers.org/hco/12/GRCh38#100419750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89412582-C-A

100419750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89412582-C-T

100419764-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89412568-A-T

100419857-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 89412475-G-C

100419866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 89412466-A-G

100419989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 89412343-C-T

100420089-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 89412243-G-T

http://identifiers.org/hco/12/GRCh38#100420176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89412171-C-A

http://identifiers.org/hco/12/GRCh38#100420180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89412167-C-A

100420180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: 3 prime UTR variant
orthologous variants: 89412167-C-T

http://identifiers.org/hco/12/GRCh38#100420233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89412116-C-A

100420233-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: 3 prime UTR variant
orthologous variants: 89412116-C-G

100420264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: 3 prime UTR variant
orthologous variants: 89412085-G-A

100420264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: 3 prime UTR variant
orthologous variants: 89412085-G-T

100420283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: 3 prime UTR variant
orthologous variants: 89412066-A-G

100420286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: 3 prime UTR variant
orthologous variants: 89412063-A-G

100420294-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: 3 prime UTR variant
orthologous variants: 89412055-G-C

100420344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: 3 prime UTR variant
orthologous variants: 89412008-T-C

100420378-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: 3 prime UTR variant
orthologous variants: 89411961-T-G

100420380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: 3 prime UTR variant
orthologous variants: 89411959-A-G

100420430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: 3 prime UTR variant
orthologous variants: 89411910-A-G

http://identifiers.org/hco/12/GRCh38#100420450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89411894-C-A

100420450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: 3 prime UTR variant
orthologous variants: 89411894-C-T

100420495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: 3 prime UTR variant
orthologous variants: 89411851-A-G

100420522-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: 3 prime UTR variant
orthologous variants: 89411830-T-A

100420522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: 3 prime UTR variant
orthologous variants: 89411830-T-C

100420707-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: 3 prime UTR variant
orthologous variants: 89411660-T-G

100420725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: 3 prime UTR variant
orthologous variants: 89411641-G-T

100420848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: 3 prime UTR variant
orthologous variants: 89411408-G-T

http://identifiers.org/hco/12/GRCh38#100421090-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89411004-A-C

100421136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: 3 prime UTR variant
orthologous variants: 89410958-G-A

100421229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: 3 prime UTR variant
orthologous variants: 89410840-T-C

100421342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: 3 prime UTR variant
orthologous variants: 89410754-A-G

100421377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: 3 prime UTR variant
orthologous variants: 89410724-C-T

100421490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: 3 prime UTR variant
orthologous variants: 89410611-T-C

100421554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: 3 prime UTR variant
orthologous variants: 89410549-T-C

http://identifiers.org/hco/12/GRCh38#100421607-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89410496-A-C

100421658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: 3 prime UTR variant
orthologous variants: 89410460-G-T

http://identifiers.org/hco/12/GRCh38#100421681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89410437-C-A

100421681-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: 3 prime UTR variant
orthologous variants: 89410437-C-G

100421681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: 3 prime UTR variant
orthologous variants: 89410437-C-T

http://identifiers.org/hco/12/GRCh38#100421708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89410421-C-A

100421708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: 3 prime UTR variant
orthologous variants: 89410421-C-T

http://identifiers.org/hco/12/GRCh38#100421710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89410419-C-A

100421734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: 3 prime UTR variant
orthologous variants: 89410391-T-C

100421847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: 3 prime UTR variant
orthologous variants: 89410281-T-C

100421857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: 3 prime UTR variant
orthologous variants: 89410271-C-T

100421865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: 3 prime UTR variant
orthologous variants: 89410263-C-T

100421899-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: 3 prime UTR variant
orthologous variants: 89410230-C-G

http://identifiers.org/hco/12/GRCh38#100421976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20151
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89410157-C-A