32858951-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: 5 prime UTR variant
orthologous variants: 153615410-A-T

32858974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: 5 prime UTR variant
orthologous variants: 153615421-C-T

32859068-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron_variant, undefined
orthologous variants: 153615495-T-A

32859068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron_variant, undefined
orthologous variants: 153615495-T-C

32859276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153615692-G-A

32861859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153622603-C-T

32861860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153622604-C-T

32861897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153622632-A-G

32862043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153622724-T-C

32862407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153622818-G-A

32863047-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153623054-C-G

32863047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153623054-C-T

32863106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153623115-C-T

http://identifiers.org/hco/20/GRCh38#32863454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153623384-C-A

32863454-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153623384-C-G

http://identifiers.org/hco/20/GRCh38#32863483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153623426-C-A

32863483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153623426-C-T

32863517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153623460-G-A

32863685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153623609-T-C

32863841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 153623748-A-G

32863842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 153623749-A-G

32863908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153623827-T-C

32863918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153623835-G-A

32863918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153623835-G-T

32863979-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153623894-T-A

32863979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153623894-T-C

32863979-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153623894-T-G

32864488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153624358-G-A

32864488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153624358-G-T

32864625-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153624470-C-G

32864652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153624497-C-T

32864653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153624498-G-A

32865826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153624765-A-G

32865878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153624818-G-A

32865971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153624880-G-T

32867373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153625335-G-T

32867504-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153625474-C-G

32867504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153625474-C-T

32867639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: missense variant
orthologous variants: 153625621-A-G

32867676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: missense variant
orthologous variants: 153625655-C-T

32867689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: synonymous variant
orthologous variants: 153625668-T-C

32867689-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: synonymous variant
orthologous variants: 153625668-T-G

32867737-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: missense variant
orthologous variants: 153625716-C-G

32867765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153625744-G-A

http://identifiers.org/hco/20/GRCh38#32867832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153625796-C-A

32867832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153625796-C-T

32868492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153625924-G-A

32869260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153626361-G-A

32869260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153626361-G-T

32869263-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153626364-G-T

32869878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153626867-C-T

http://identifiers.org/hco/20/GRCh38#32870105-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153627089-A-C

32870105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153627089-A-G

http://identifiers.org/hco/20/GRCh38#32870127-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153627111-A-C

32870128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153627112-A-G

32875878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153629512-G-A

32875878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153629512-G-T

32875888-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153629522-T-A

32875888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153629522-T-C

32875921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 153629549-T-C

32875985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 153629613-G-A

32875985-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 153629613-G-C

http://identifiers.org/hco/20/GRCh38#32875993-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153629621-A-C

32875993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 153629621-A-G

32876161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153629782-G-A

http://identifiers.org/hco/20/GRCh38#32876413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153630020-C-A

32876413-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153630020-C-G

32878824-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153631195-T-G

32879042-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153631385-T-G

32879197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153631525-G-A

32879247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153631564-G-A

32879275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153631592-C-T

32879401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153631709-C-T

32879402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153631710-C-T

32879507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153631772-A-G

32879559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153631820-C-T

32879560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153631821-G-A

32879997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153632773-G-A

32880209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153632981-G-A

32880592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153633064-G-A

32884188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153633337-G-A

32884235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153633385-A-G

32884359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153633506-G-A

32884396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153633541-T-C

32884603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153633735-T-C

32884627-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153633762-A-T

32884669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153633803-A-G

32885124-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153634210-C-G

32885124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153634210-C-T

32885331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153634422-G-A

32885348-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153634464-G-C

32885397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153634535-T-C

32885424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153634562-G-A

32885424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153634562-G-T

32885679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153634788-T-C

http://identifiers.org/hco/20/GRCh38#32885693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153634802-C-A

32885693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153634802-C-T

32885873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153634949-C-T

32886101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153635118-G-A

32886454-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153635474-A-T

32886483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153635502-G-A

32886483-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153635502-G-C

32886634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153635791-C-T

32886765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153635923-G-T

32886772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153635930-C-T

32889133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153636125-G-A

32889220-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153636207-T-A

32889345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: synonymous variant
orthologous variants: 153636331-T-C

32889419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153636408-G-T

32889510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153636485-G-T

32889539-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153636512-G-T

32889627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153636633-C-T

32890268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153636991-G-A

32890423-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153637127-G-C

32890423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153637127-G-T

32890507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153637210-G-A

32890535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153637238-A-G

32892188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153639535-A-G

32892244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: synonymous variant
orthologous variants: 153639594-C-T

32892339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153639671-C-T

http://identifiers.org/hco/20/GRCh38#32892382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153639716-C-A

32892417-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153639753-T-A

http://identifiers.org/hco/20/GRCh38#32892420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153639756-C-A

32892420-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153639756-C-G

32892420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153639756-C-T

32892512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153639830-G-T

http://identifiers.org/hco/20/GRCh38#32892522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153639840-C-A

32892689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153639962-C-T

http://identifiers.org/hco/20/GRCh38#32893145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153640448-C-A

32893145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153640448-C-T

32893147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153640449-A-G

32893147-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153640449-A-T

32893158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153640460-C-T

32893261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: synonymous variant
orthologous variants: 153640563-G-A

32893285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: missense variant
orthologous variants: 153640587-G-T

32893286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: missense variant
orthologous variants: 153640588-G-A

32893286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: missense variant
orthologous variants: 153640588-G-T

32893319-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153640615-G-C

32893339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153640635-G-A

32893408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153640706-T-C

http://identifiers.org/hco/20/GRCh38#32893448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153640744-C-A

32893448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153640744-C-T

32894070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153641770-A-G

32894121-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153641822-C-G

32894121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153641822-C-T

32894463-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153642273-G-C

32894463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153642273-G-T

32894657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153642450-T-C

32896183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153644060-C-T

32896283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153644139-G-A

http://identifiers.org/hco/20/GRCh38#32896318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153644171-C-A

32896318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153644171-C-T

32896321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153644174-G-A

32896321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153644174-G-T

32896361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153644206-G-A

32896367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153644212-A-G

32896367-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153644212-A-T

32896626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153644447-G-A

32896626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153644447-G-T

32896918-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153644739-C-G

32897348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153645343-G-A

32897465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153645511-C-T

32897529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153645612-A-G

32897563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153645676-C-T

http://identifiers.org/hco/20/GRCh38#32897735-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153645921-A-C

32897837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153646005-G-A

32898140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153646401-G-A

http://identifiers.org/hco/20/GRCh38#32898277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153646578-C-A

32898277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153646578-C-T

32898335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153646639-G-T

32898341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153646645-G-A

32898341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153646645-G-T

http://identifiers.org/hco/20/GRCh38#32898371-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153646683-A-C

32898375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153646687-G-A

32898375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153646687-G-T

32898397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 153646709-G-A

32898397-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 153646709-G-T

32898436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 153646747-T-C

http://identifiers.org/hco/20/GRCh38#32898453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153646767-C-A

32898640-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 153646947-T-A

32901725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 153648772-G-A

32901965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 153649000-C-T

32902100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 153649120-C-T

32902170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 153649189-G-T

32902194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 153649213-G-A

32902746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 153649612-T-C

32902960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 153649826-C-T

http://identifiers.org/hco/20/GRCh38#32903088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153649917-C-A

32903146-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 153649955-C-G

32903304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 153650075-G-A

32903304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 153650075-G-T

32903324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 153650095-G-A

http://identifiers.org/hco/20/GRCh38#32903325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153650096-C-A

32903325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 153650096-C-T

32903350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 153650118-C-T

http://identifiers.org/hco/20/GRCh38#32903361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153650132-C-A

32903363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 153650134-A-G

http://identifiers.org/hco/20/GRCh38#32903368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153650138-C-A

32903368-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 153650138-C-G

32903368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 153650138-C-T

32903433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 153650203-C-T

32903447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 153650217-C-T

32903512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 153650270-T-C

32903512-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 153650270-T-G

32903592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 153650337-C-T

http://identifiers.org/hco/20/GRCh38#32906484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153651667-C-A

32906484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153651667-C-T

32906619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: missense variant
orthologous variants: 153651805-G-T

http://identifiers.org/hco/20/GRCh38#32906651-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153651838-C-A

32906651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153651838-C-T

32906688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153651876-G-A

32906688-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153651876-G-C

32906688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153651876-G-T

32906725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153651913-G-T

32906789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153652073-G-A

32906789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153652073-G-T

http://identifiers.org/hco/20/GRCh38#32907085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153652386-C-A

32907094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153652395-A-G

32907102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153652403-A-G

http://identifiers.org/hco/20/GRCh38#32907114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153652415-C-A

32907144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153652441-G-A

32907144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153652441-G-T

32907959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153652527-G-A

32908063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153652630-G-A

32908063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153652630-G-T

32908122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153652677-G-A

32908146-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153652702-T-A

32908146-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153652702-T-G

http://identifiers.org/hco/20/GRCh38#32908194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153652721-C-A

32908194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153652721-C-T

http://identifiers.org/hco/20/GRCh38#32908301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153652818-C-A

32908379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: missense variant
orthologous variants: 153652893-G-T

32908382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: synonymous variant
orthologous variants: 153652896-G-A

http://identifiers.org/hco/20/GRCh38#32908420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153652934-C-A

32908420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 153652934-C-T

http://identifiers.org/hco/20/GRCh38#32908450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153652947-C-A

32908450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153652947-C-T

32908583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153653027-T-C

32908707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153653105-G-A

32908774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153653169-C-T

32908777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153653172-T-C

32908903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153653290-A-G

32908903-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153653290-A-T

32909015-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153653364-G-C

http://identifiers.org/hco/20/GRCh38#32909068-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153653386-A-C

32909181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153653485-G-A

32909571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153654330-C-T

32909672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153654424-T-C

32909715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153654452-A-G

http://identifiers.org/hco/20/GRCh38#32909719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153654456-C-A

32909719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153654456-C-T

32909728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153654465-G-A

32909728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153654465-G-T

http://identifiers.org/hco/20/GRCh38#32909751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153654487-C-A

32909751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153654487-C-T

http://identifiers.org/hco/20/GRCh38#32909760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153654496-C-A

32909760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153654496-C-T

32909842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: synonymous variant
orthologous variants: 153654565-T-C

32909842-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: missense variant
orthologous variants: 153654565-T-G

http://identifiers.org/hco/20/GRCh38#32909952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153654674-C-A

http://identifiers.org/hco/20/GRCh38#32909987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153654705-C-A

32909987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153654705-C-T

http://identifiers.org/hco/20/GRCh38#32909998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153654720-C-A

32909998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153654720-C-T

32910031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153654764-A-G

http://identifiers.org/hco/20/GRCh38#32910052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153654785-C-A

32910052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153654785-C-T

32910054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153654787-G-T

32910260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153654955-G-A

32910260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153654955-G-T

32910443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153655121-G-A

http://identifiers.org/hco/20/GRCh38#32911350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153656203-C-A

32911350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153656203-C-T

32911405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153656243-A-G

32911405-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153656243-A-T

32911427-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153656262-G-C

32911427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153656262-G-T

32911587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: synonymous variant
orthologous variants: 153656406-C-T

32911777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153656568-G-A

32911778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153656569-G-A

32911823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 153656612-T-C

32911838-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 153656627-T-A

32911926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153656688-A-G

32912708-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153658205-G-C

32912708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153658205-G-T

32912754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153658251-T-C

32912882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153658376-A-G

32913277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153658715-A-G

32913620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153659157-T-C

http://identifiers.org/hco/20/GRCh38#32913698-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153659232-A-C

32913745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153659279-C-T

32913762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153659296-C-T

http://identifiers.org/hco/20/GRCh38#32913958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153659723-C-A

32913989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153659752-G-A

32914179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153659926-C-T

32914210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153659957-T-C

32914361-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153660083-C-G

32914361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153660083-C-T

32915653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153660874-A-G

http://identifiers.org/hco/20/GRCh38#32915671-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153660892-A-C

32915671-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153660892-A-T

32915689-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153660910-T-A

32915828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153661003-C-T

http://identifiers.org/hco/20/GRCh38#32916029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153661185-C-A

32916634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153661609-C-T

32916763-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153661717-T-A

32916799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153661753-A-G

32916919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153661857-T-C

32916919-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153661857-T-G

http://identifiers.org/hco/20/GRCh38#32916929-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153661867-A-C

32916929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153661867-A-G

http://identifiers.org/hco/20/GRCh38#32916937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153661875-C-A

32916937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153661875-C-T

http://identifiers.org/hco/20/GRCh38#32916941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153661879-C-A

32916941-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153661879-C-G

32916941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153661879-C-T

http://identifiers.org/hco/20/GRCh38#32916970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153661908-C-A

32916970-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153661908-C-G

32916970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153661908-C-T

http://identifiers.org/hco/20/GRCh38#32917030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153661966-C-A

32917030-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153661966-C-G

http://identifiers.org/hco/20/GRCh38#32917110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153662019-C-A

32917110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 153662019-C-T

32917122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 153662031-G-A

32917122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 153662031-G-T

32917193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 153662112-T-C

32917598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 153662545-G-T

32918006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 153664113-C-T

http://identifiers.org/hco/20/GRCh38#32918217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153664319-C-A

32918272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 153664374-G-A

32918272-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 153664374-G-C

32918272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 153664374-G-T

32918338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 153664429-G-A

32918475-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 153664544-G-C

32918571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 153664630-G-A

32918571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 153664630-G-T

32918587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 153664645-G-A

32918602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 153664653-T-C

32919168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 153665000-G-A

32919598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 153665267-G-A

32919912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 153665492-A-G

http://identifiers.org/hco/20/GRCh38#32919977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153665549-C-A

32919977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 153665549-C-T

32919978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 153665550-T-C

32919978-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 153665550-T-G

http://identifiers.org/hco/20/GRCh38#32920020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153665593-C-A

32920020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 153665593-C-T

32920152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 153665742-T-C

32920247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153665818-G-A

32925591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153666209-G-T

32925644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153666267-C-T

32925742-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153666374-T-A

32925758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153666399-C-T

32925759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153666400-G-A

32925759-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153666400-G-C

32925867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153666520-C-T

32925896-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153666549-T-G

32925936-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153666601-C-G

32925936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153666601-C-T

32926102-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153666765-G-C

32926114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153666770-C-T

32926136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153666791-C-T

32926154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153666807-G-A

32926464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153667142-G-T

32926467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153667145-G-A

32926467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153667145-G-T

http://identifiers.org/hco/20/GRCh38#32926503-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153667181-A-C

32926503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153667181-A-G

32926503-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153667181-A-T

http://identifiers.org/hco/20/GRCh38#32926504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153667182-C-A

32926504-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153667182-C-G

32926504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153667182-C-T

32929323-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153671955-G-C

32929494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153672168-T-C

32929991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153672935-A-G

32930127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153673065-A-G

32930143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153673082-C-T

32930154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153673093-G-T

32930231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153673157-G-A

32930341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153673246-G-A

32930341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153673246-G-T

http://identifiers.org/hco/20/GRCh38#32930344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153673249-C-A

32930451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: synonymous variant
orthologous variants: 153673353-C-T

32930475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: synonymous variant
orthologous variants: 153673377-C-T

32930490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: synonymous variant
orthologous variants: 153673392-T-C

32930490-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: missense variant
orthologous variants: 153673392-T-G

32930496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: synonymous variant
orthologous variants: 153673398-T-C

32930496-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: missense variant
orthologous variants: 153673398-T-G

32930629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153673531-T-C

http://identifiers.org/hco/20/GRCh38#32930671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153673553-C-A

32930710-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153673593-T-A

32930752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153673638-G-A

32930752-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153673638-G-C

32930789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153673662-G-A

32930865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153673738-C-T

32931212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: missense variant
orthologous variants: 153674070-A-G

32931220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: missense variant
orthologous variants: 153674078-C-T

32931222-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: synonymous variant
orthologous variants: 153674080-A-T

32931243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: synonymous variant
orthologous variants: 153674101-G-A

32931291-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: missense variant
orthologous variants: 153674149-A-T

http://identifiers.org/hco/20/GRCh38#32931300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153674158-C-A

32931306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: synonymous variant
orthologous variants: 153674164-C-T

http://identifiers.org/hco/20/GRCh38#32931360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153674218-C-A

32931360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153674218-C-T

http://identifiers.org/hco/20/GRCh38#32931385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153674243-C-A

32943105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153680175-A-G

32943659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 153680809-C-T

32943729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron_variant, missense_variant
orthologous variants: 153680879-G-A

32943729-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron_variant, missense_variant
orthologous variants: 153680879-G-C

32943746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 153680896-T-C

http://identifiers.org/hco/20/GRCh38#32943764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153680914-C-A

32943764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 153680914-C-T

32943853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153680991-T-C

32943854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153680992-G-A

32943860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153680998-G-A

32943860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153680998-G-T

32943877-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153681017-T-A

32943877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153681017-T-C

32943877-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153681017-T-G

32943886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153681026-T-C

http://identifiers.org/hco/20/GRCh38#32943989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153681133-C-A

http://identifiers.org/hco/20/GRCh38#32958253-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153682916-A-C

32958305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153682968-G-A

32958305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153682968-G-T

32958313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153682976-T-C

32958314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153682977-G-A

32958314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153682977-G-T

32958377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153682994-G-A

32958377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153682994-G-T

32958449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 153683066-A-G

32958526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: missense variant
orthologous variants: 153683146-A-G

http://identifiers.org/hco/20/GRCh38#32958566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153683186-C-A

32959226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153684276-T-C

32959657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153684655-A-G

32959657-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153684655-A-T

http://identifiers.org/hco/20/GRCh38#32959749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153684785-C-A

http://identifiers.org/hco/20/GRCh38#32959848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153684875-C-A

32959849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: missense variant
orthologous variants: 153684876-A-G

32959895-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: missense variant
orthologous variants: 153684922-G-T

32959910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: synonymous variant
orthologous variants: 153684937-C-T

32959927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: missense_variant, undefined
orthologous variants: 153684952-G-A

32959927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: missense_variant, undefined
orthologous variants: 153684952-G-T

32959940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: synonymous_variant, undefined
orthologous variants: 153684967-C-T

32960031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153685043-G-A

32960031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153685043-G-T

32960177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153685190-G-A

http://identifiers.org/hco/20/GRCh38#32960232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153685229-C-A

32960232-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153685229-C-G

32960232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153685229-C-T

32960278-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153685242-T-A

32960278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153685242-T-C

http://identifiers.org/hco/20/GRCh38#32960283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153685247-C-A

32960283-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153685247-C-G

32960307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153685264-A-G

32960307-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153685264-A-T

32960553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153685474-C-T

32960699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153685623-C-T

32960759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153685679-G-T

http://identifiers.org/hco/20/GRCh38#32960892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153685818-C-A

32960921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153685831-G-A

32960998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153685904-G-A

32960998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153685904-G-T

http://identifiers.org/hco/20/GRCh38#32961029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153685927-C-A

32961029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153685927-C-T

32961061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153685947-G-A

32961061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153685947-G-T

32961064-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153685950-T-A

32961064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153685950-T-C

32961089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153685975-G-A

http://identifiers.org/hco/20/GRCh38#32961091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153685977-C-A

32961097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: intron variant
orthologous variants: 153685983-C-T

32961227-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: missense variant
orthologous variants: 153686103-A-T

32961307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: missense variant
orthologous variants: 153686183-A-G

32961331-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: missense variant
orthologous variants: 153686207-T-G

http://identifiers.org/hco/20/GRCh38#32961332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153686208-C-A

32961332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: missense variant
orthologous variants: 153686208-C-T

32961333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: synonymous variant
orthologous variants: 153686209-C-T

32961403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: synonymous variant
orthologous variants: 153686264-C-T

http://identifiers.org/hco/20/GRCh38#32961420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153686284-C-A

http://identifiers.org/hco/20/GRCh38#32961450-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153686314-A-C

32961450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: synonymous variant
orthologous variants: 153686314-A-G

http://identifiers.org/hco/20/GRCh38#32961477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153686341-C-A

32961477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: synonymous variant
orthologous variants: 153686341-C-T

32961544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: missense variant
orthologous variants: 153686407-C-T

http://identifiers.org/hco/20/GRCh38#32961564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153686427-C-A

32961564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: synonymous variant
orthologous variants: 153686427-C-T

http://identifiers.org/hco/20/GRCh38#32961570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153686433-C-A

32961570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: synonymous variant
orthologous variants: 153686433-C-T

http://identifiers.org/hco/20/GRCh38#32961640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#153686501-C-A

32961640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: 3 prime UTR variant
orthologous variants: 153686501-C-T

32961658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: 3 prime UTR variant
orthologous variants: 153686513-G-A

32961658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: 3 prime UTR variant
orthologous variants: 153686513-G-T

32961681-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: 3 prime UTR variant
orthologous variants: 153686535-T-G

32961699-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: 3 prime UTR variant
orthologous variants: 153686553-G-C

32961741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: 3 prime UTR variant
orthologous variants: 153686591-G-A

32961741-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: 3 prime UTR variant
orthologous variants: 153686591-G-C

32961741-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: 3 prime UTR variant
orthologous variants: 153686591-G-T

32961746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34532
most severe consequence: 3 prime UTR variant
orthologous variants: 153686596-A-G