85027826-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 5 prime UTR variant
orthologous variants: 120840952-C-G

85028032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120841179-C-T

85029176-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120841709-G-C

85029608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120842100-G-A

85029608-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120842100-G-C

85029744-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120842455-C-G

85029754-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120842510-A-T

85030020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120842807-G-A

http://identifiers.org/hco/16/GRCh38#85030074-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#120842857-A-C

85030074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron_variant, undefined
orthologous variants: 120842857-A-G

85030079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron_variant, undefined
orthologous variants: 120842862-A-G

85030119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron_variant, undefined
orthologous variants: 120842899-C-T

85030294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120843078-G-T

85030344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120843130-G-A

85030987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120843431-A-G

85031931-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120844194-C-G

85032039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120844315-A-G

85032043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120844319-A-G

85032154-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120844424-G-C

http://identifiers.org/hco/16/GRCh38#85032190-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120844459-A-C

85032205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120844474-G-A

85032339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120844558-T-C

85033063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120844889-T-C

85033481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120845128-G-A

85033481-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120845128-G-C

85034082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120845787-G-A

85034532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120845913-G-A

85034532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120845913-G-T

http://identifiers.org/hco/16/GRCh38#85034557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120845938-C-A

85034557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120845938-C-T

85034698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120846068-C-T

85034762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120846129-G-A

85036393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120846945-G-A

85036393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120846945-G-T

85036438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120846974-C-T

85036615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120847207-G-A

85036615-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120847207-G-T

85036633-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120847225-G-C

85036728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron_variant, undefined
orthologous variants: 120847376-G-T

85036770-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron_variant, undefined
orthologous variants: 120847410-C-G

85037116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron_variant, undefined
orthologous variants: 120847763-A-G

http://identifiers.org/hco/16/GRCh38#85037512-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#120848126-A-C

85037512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron_variant, undefined
orthologous variants: 120848126-A-G

85037564-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120848167-T-G

85040636-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120849865-G-C

85040808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120850029-T-C

http://identifiers.org/hco/16/GRCh38#85040954-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120850145-A-C

85040954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120850145-A-G

85040954-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120850145-A-T

85040963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120850153-A-G

85040972-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120850162-C-G

85041025-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120850213-A-T

85041055-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120850238-T-G

85041201-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120850382-A-T

85041260-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120850441-C-G

85041260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120850441-C-T

85044288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120853598-C-T

http://identifiers.org/hco/16/GRCh38#85044295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120853605-C-A

85049352-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120860226-C-G

85049375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120860249-G-A

85049380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120860254-C-T

85049381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120860255-G-A

85049398-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120860272-C-G

85052592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120861917-C-T

85052599-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120861924-T-G

http://identifiers.org/hco/16/GRCh38#85052622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120861954-C-A

85052622-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120861954-C-G

85056020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron_variant, undefined
orthologous variants: 120862793-T-C

85056108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron_variant, undefined
orthologous variants: 120862860-T-C

85057975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120863405-G-A

http://identifiers.org/hco/16/GRCh38#85058050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120863476-C-A

85058050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120863476-C-T

85058089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120863511-G-A

85058839-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120863866-T-G

85059061-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120864059-C-G

85064440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120869703-C-T

85064589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120869826-T-C

85064627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120869834-C-T

85064766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120869907-A-G

http://identifiers.org/hco/16/GRCh38#85064964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120870141-C-A

85064964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120870141-C-T

85064990-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120870167-T-G

85064992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120870169-G-A

85065086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120870311-C-T

85065178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120870398-G-A

85065178-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120870398-G-C

85065238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120870458-A-G

85065244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120870464-A-G

85065289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120870513-G-A

85065731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120870959-A-G

85065735-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120870963-G-C

85065772-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120870998-C-G

85065834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120871069-A-G

85066444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120871537-G-A

85066537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120871623-G-A

85066578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120871659-T-C

85066659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120871688-C-T

85066724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120871746-T-C

85066724-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120871746-T-G

http://identifiers.org/hco/16/GRCh38#85066732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120871754-C-A

85066732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120871754-C-T

85066740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120871762-G-A

85066849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120871852-G-A

85066849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120871852-G-T

85066859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120871874-G-A

85066859-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120871874-G-C

85066859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120871874-G-T

85066902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 5_prime_UTR_variant, splice_region_variant
orthologous variants: 120871944-G-T

http://identifiers.org/hco/16/GRCh38#85066903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120871945-C-A

85066903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 5 prime UTR variant
orthologous variants: 120871945-C-T

http://identifiers.org/hco/16/GRCh38#85066936-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120871975-A-C

85066936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 5 prime UTR variant
orthologous variants: 120871975-A-G

85066958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 5 prime UTR variant
orthologous variants: 120871997-T-C

85067155-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: synonymous variant
orthologous variants: 120872157-C-G

85067155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: synonymous variant
orthologous variants: 120872157-C-T

85067290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: synonymous variant
orthologous variants: 120872292-C-T

85067433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120872429-G-A

http://identifiers.org/hco/16/GRCh38#85067440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120872436-C-A

85067440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120872436-C-T

http://identifiers.org/hco/16/GRCh38#85071439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120875773-C-A

85071439-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120875773-C-G

http://identifiers.org/hco/16/GRCh38#85071551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120875868-C-A

85071551-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120875868-C-G

85071553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120875870-C-T

85071619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120875935-C-T

85071642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120875940-G-T

http://identifiers.org/hco/16/GRCh38#85071684-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120875963-A-C

85071684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120875963-A-G

85071804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: synonymous variant
orthologous variants: 120876052-G-A

85071804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: missense variant
orthologous variants: 120876052-G-T

85071823-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: missense variant
orthologous variants: 120876071-T-A

85071849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: synonymous variant
orthologous variants: 120876097-C-T

85071861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: synonymous variant
orthologous variants: 120876109-T-C

http://identifiers.org/hco/16/GRCh38#85071967-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120876183-A-C

85071967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120876183-A-G

85072385-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120876403-A-T

85072547-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120876514-A-T

http://identifiers.org/hco/16/GRCh38#85072567-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120876534-A-C

85072650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120876607-G-A

http://identifiers.org/hco/16/GRCh38#85072823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120876755-C-A

85072823-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120876755-C-G

85072823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120876755-C-T

http://identifiers.org/hco/16/GRCh38#85072896-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120876794-C-A

85072896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120876794-C-T

85073020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120876906-A-G

85073024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120876910-T-C

85073148-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120877002-G-T

85073163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120877011-C-T

85075604-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120877754-C-G

85075629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120877774-G-A

http://identifiers.org/hco/16/GRCh38#85075689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120877832-C-A

85075718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120877849-G-A

85075718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120877849-G-T

85075723-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120877854-T-G

85075741-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120877869-T-A

85075741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120877869-T-C

85075741-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120877869-T-G

85075765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120877895-G-T

85075781-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120877910-A-T

85075789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120877918-G-A

85075789-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120877918-G-C

85075792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120877921-G-A

85075792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120877921-G-T

http://identifiers.org/hco/16/GRCh38#85075794-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120877923-A-C

85075802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120877985-G-A

85075802-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120877985-G-C

85075962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120878169-T-C

85075963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120878170-G-A

85075963-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120878170-G-C

85076052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120878251-G-T

http://identifiers.org/hco/16/GRCh38#85076232-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120878369-A-C

85076375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120878454-G-T

85076450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120878511-G-A

85076496-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120878556-C-G

85076592-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120878639-C-G

85076607-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120878646-C-G

85076607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120878646-C-T

85076639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120878661-C-T

http://identifiers.org/hco/16/GRCh38#85076721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120878705-C-A

85077172-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120878906-C-G

85077197-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120878928-G-C

85077197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120878928-G-T

http://identifiers.org/hco/16/GRCh38#85077235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120878966-C-A

85077235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120878966-C-T

85077380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120879130-T-C

85077381-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120879131-A-T

http://identifiers.org/hco/16/GRCh38#85077384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120879134-C-A

85077384-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120879134-C-G

85077384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120879134-C-T

85077428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: missense variant
orthologous variants: 120879181-A-G

85077428-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: missense variant
orthologous variants: 120879181-A-T

http://identifiers.org/hco/16/GRCh38#85077757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120879470-C-A

85077757-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120879470-C-G

http://identifiers.org/hco/16/GRCh38#85077807-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120879510-C-A

85077807-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120879510-C-G

85077807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120879510-C-T

85077967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120879727-G-A

85077967-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120879727-G-C

85077967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120879727-G-T

85078081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120879883-T-C

85078221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120880017-A-G

85078221-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120880017-A-T

85078226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120880022-C-T

85078727-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120880503-C-G

http://identifiers.org/hco/16/GRCh38#85078809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120880554-C-A

85078809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120880554-C-T

85078843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120880589-T-C

85078843-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120880589-T-G

http://identifiers.org/hco/16/GRCh38#85078875-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120880614-A-C

85078875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120880614-A-G

85079017-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 120880748-C-G

85079017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 120880748-C-T

85079018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 120880749-G-A

85079018-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 120880749-G-C

85079018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 120880749-G-T

http://identifiers.org/hco/16/GRCh38#85079120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120880839-C-A

85079120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 120880839-C-T

85079128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 120880848-G-A

85079128-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 120880848-G-T

http://identifiers.org/hco/16/GRCh38#85079186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120880905-C-A

85079186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 120880905-C-T

85079241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 120880937-G-A

85079241-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 120880937-G-C

85079241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 120880937-G-T

85079248-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 120880943-T-A

85079248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 120880943-T-C

http://identifiers.org/hco/16/GRCh38#85079272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120880963-C-A

85079272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 120880963-C-T

85081297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120883019-T-C

85081298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120883020-G-A

85081298-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120883020-G-C

http://identifiers.org/hco/16/GRCh38#85081486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120883208-C-A

85081486-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120883208-C-G

85081683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120883393-C-T

85081935-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120883614-A-T

85082290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120883955-A-G

85082379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120884025-G-A

85082487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120884134-G-A

85082641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120884282-G-T

85082899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120884435-G-A

85082962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120884453-C-T

85083103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120884560-G-A

85083105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120884562-C-T

85084874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120885300-G-A

85084878-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120885305-G-C

85085094-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120885474-A-T

85085115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120885495-A-G

85085134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120885514-G-T

85085333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120885643-G-A

85085696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120886042-G-A

85085696-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120886042-G-C

85085972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120886251-G-T

85086045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120886278-C-T

85086233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120886438-G-A

85086238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120886443-G-T

85086450-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120886553-A-T

85086563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120886633-C-T

http://identifiers.org/hco/16/GRCh38#85086614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120886670-C-A

85086614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120886670-C-T

85086629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120886683-C-T

85086692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: synonymous variant
orthologous variants: 120886746-G-A

85086692-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: synonymous variant
orthologous variants: 120886746-G-C

85086692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: synonymous variant
orthologous variants: 120886746-G-T

85086778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120886801-G-A

85086778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron variant
orthologous variants: 120886801-G-T

http://identifiers.org/hco/16/GRCh38#85086874-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#120886859-A-C

85086874-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron_variant, undefined
orthologous variants: 120886859-A-T

http://identifiers.org/hco/16/GRCh38#85086920-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#120886900-A-C

85086920-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 120886900-A-T

85086924-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 120886904-G-C

85086924-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 120886904-G-T

85086998-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120886981-G-C

http://identifiers.org/hco/16/GRCh38#85087246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120887217-C-A

85087246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120887217-C-T

85087414-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120887343-G-C

85087533-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120887441-C-G

85087587-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120887480-T-A

85087691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120887560-A-G

85087778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120887631-C-T

85087839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120887684-G-A

85087928-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120887725-G-C

85088019-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120887815-T-G

85088081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120887836-G-T

http://identifiers.org/hco/16/GRCh38#85088234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120887916-C-A

85088234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120887916-C-T

85088364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120888015-G-A

85088364-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120888015-G-C

85088364-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120888015-G-T

http://identifiers.org/hco/16/GRCh38#85088369-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120888020-A-C

85088369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120888020-A-G

85088370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120888021-T-C

http://identifiers.org/hco/16/GRCh38#85088375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120888026-C-A

http://identifiers.org/hco/16/GRCh38#85088447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120888089-C-A

85088447-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120888089-C-G

85088447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120888089-C-T

http://identifiers.org/hco/16/GRCh38#85088476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120888118-C-A

85088476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120888118-C-T

http://identifiers.org/hco/16/GRCh38#85088559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120888192-C-A

85088559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120888192-C-T

http://identifiers.org/hco/16/GRCh38#85088580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120888222-C-A

85088580-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120888222-C-G

85088580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120888222-C-T

85088612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120888252-G-A

85088612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120888252-G-T

85088632-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120888282-T-A

85088632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120888282-T-C

85088632-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120888282-T-G

85088635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120888285-G-A

85088635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120888285-G-T

85088678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120888331-G-A

85088678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120888331-G-T

85090598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3 prime UTR variant
orthologous variants: 120889612-G-T

85090624-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3 prime UTR variant
orthologous variants: 120889628-T-A

http://identifiers.org/hco/16/GRCh38#85090664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120889663-C-A

85090664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3 prime UTR variant
orthologous variants: 120889663-C-T

85090767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3 prime UTR variant
orthologous variants: 120889769-G-A

http://identifiers.org/hco/16/GRCh38#85090798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120889810-C-A

85090826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3 prime UTR variant
orthologous variants: 120889836-T-C

http://identifiers.org/hco/16/GRCh38#85090865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120889879-C-A

85090865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3 prime UTR variant
orthologous variants: 120889879-C-T

85090885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3 prime UTR variant
orthologous variants: 120889899-C-T

85090886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3 prime UTR variant
orthologous variants: 120889900-T-C

85090910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3 prime UTR variant
orthologous variants: 120889937-A-G

http://identifiers.org/hco/16/GRCh38#85093402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120891306-C-A

85093455-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3 prime UTR variant
orthologous variants: 120891347-T-G

85093463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3 prime UTR variant
orthologous variants: 120891356-A-G

http://identifiers.org/hco/16/GRCh38#85093507-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120891403-A-C

85093513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3 prime UTR variant
orthologous variants: 120891409-G-T

85093524-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3 prime UTR variant
orthologous variants: 120891420-C-G

85093554-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3 prime UTR variant
orthologous variants: 120891446-G-C

85093554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3 prime UTR variant
orthologous variants: 120891446-G-T

85093565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3 prime UTR variant
orthologous variants: 120891460-C-T

http://identifiers.org/hco/16/GRCh38#85093631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120891524-C-A

85093781-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 120891650-A-T

85093789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3 prime UTR variant
orthologous variants: 120891658-G-A

85093789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3 prime UTR variant
orthologous variants: 120891658-G-T

85093797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3 prime UTR variant
orthologous variants: 120891666-A-G

http://identifiers.org/hco/16/GRCh38#85093890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#120891754-C-A

85093974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 120891819-T-C

http://identifiers.org/hco/16/GRCh38#85093975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#120891820-C-A

85094001-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 120891841-C-G

85094044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29058
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 120891870-T-C