93566681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 38085535-A-G

93566681-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 38085535-A-T

http://identifiers.org/hco/10/GRCh38#93566683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#38085537-C-A

93566683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 38085537-C-T

http://identifiers.org/hco/10/GRCh38#93566689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38085543-C-A

93566689-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 5 prime UTR variant
orthologous variants: 38085543-C-G

93566744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: synonymous variant
orthologous variants: 38085598-A-G

93566744-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: synonymous variant
orthologous variants: 38085598-A-T

93566749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: missense variant
orthologous variants: 38085603-G-A

93566749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: missense variant
orthologous variants: 38085603-G-T

93566843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: synonymous variant
orthologous variants: 38085697-G-A

93566843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: synonymous variant
orthologous variants: 38085697-G-T

93566897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: synonymous_variant, undefined
orthologous variants: 38085751-G-A

http://identifiers.org/hco/10/GRCh38#93567044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#38085898-C-A

93567044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: synonymous_variant, undefined
orthologous variants: 38085898-C-T

93567173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: synonymous variant
orthologous variants: 38086027-G-A

93567173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: synonymous variant
orthologous variants: 38086027-G-T

http://identifiers.org/hco/10/GRCh38#93567187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38086041-C-A

93567187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: missense variant
orthologous variants: 38086041-C-T

93567221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: synonymous_variant, undefined
orthologous variants: 38086075-G-A

93567221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: synonymous_variant, undefined
orthologous variants: 38086075-G-T

http://identifiers.org/hco/10/GRCh38#93567346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38086205-C-A

93567346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38086205-C-T

93567389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38086267-A-G

93567389-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38086267-A-T

93567498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38086382-G-T

93567501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38086385-T-C

93568708-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38086809-G-C

93569318-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38087496-C-G

93569327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38087505-T-C

93569385-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38087569-A-T

93569644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38087749-G-A

93569720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38087811-T-C

93569721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38087812-C-T

http://identifiers.org/hco/10/GRCh38#93570253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38088715-C-A

93570298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38088760-A-G

93570307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38088769-G-A

93570314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38088776-A-G

93570365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38088834-A-G

93570365-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38088834-A-T

http://identifiers.org/hco/10/GRCh38#93570445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38089068-C-A

http://identifiers.org/hco/10/GRCh38#93570459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38089083-C-A

http://identifiers.org/hco/10/GRCh38#93570499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38089123-C-A

93570499-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38089123-C-G

93570696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38089266-A-G

93570853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38089386-C-T

93570989-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38089501-C-G

93570994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38089506-G-A

93571172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38089679-G-T

93571615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38090104-C-T

93571616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38090105-G-A

93571642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38090133-T-C

93571844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38090557-C-T

http://identifiers.org/hco/10/GRCh38#93574264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38092605-C-A

93574390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38092723-T-C

93574438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38092771-G-A

93574510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38092832-G-A

93574992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38094288-C-T

93575015-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38094320-T-A

93575207-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38094484-C-G

93575416-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38094680-C-G

http://identifiers.org/hco/10/GRCh38#93575562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38095338-C-A

93575562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38095338-C-T

93576033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38095771-G-A

93576277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38096012-T-C

http://identifiers.org/hco/10/GRCh38#93576305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38096045-C-A

93576305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38096045-C-T

http://identifiers.org/hco/10/GRCh38#93576322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38096061-C-A

93576388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38096161-A-G

93576506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38096270-C-T

93576741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38096412-A-G

93576910-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38096594-G-C

93577286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38096968-G-A

93577622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38097257-A-G

93577630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38097265-T-C

93577839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38097526-C-T

93577902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38097586-C-T

93578013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38097683-A-G

93580648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 38098357-A-G

93580676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 38098385-G-A

93580690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 38098399-C-T

93580816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron_variant, undefined
orthologous variants: 38098511-C-T

http://identifiers.org/hco/10/GRCh38#93580834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#38098528-C-A

93580865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron_variant, undefined
orthologous variants: 38098559-C-T

http://identifiers.org/hco/10/GRCh38#93580875-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#38098569-A-C

93580982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron_variant, undefined
orthologous variants: 38098676-G-A

http://identifiers.org/hco/10/GRCh38#93581172-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38098882-A-C

93581415-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38099618-T-A

93581499-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38099681-T-G

93581536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38099707-G-A

93581536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38099707-G-T

93581580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38099751-T-C

93581622-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38099786-G-T

93581698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38099908-G-A

93582075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38100713-T-C

93582231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38100863-T-C

http://identifiers.org/hco/10/GRCh38#93584459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38101128-C-A

93584459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38101128-C-T

93584528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38101200-A-G

93585110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38101517-C-T

93587231-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 38102074-A-T

93587248-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron_variant, missense_variant
orthologous variants: 38102091-C-G

93587248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron_variant, missense_variant
orthologous variants: 38102091-C-T

93587423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 38102266-G-A

93587423-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 38102266-G-C

93587465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 38102308-A-G

http://identifiers.org/hco/10/GRCh38#93587555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38102398-C-A

93587555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 38102398-C-T

http://identifiers.org/hco/10/GRCh38#93587638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38102467-C-A

93587759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38102589-G-A

93587759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38102589-G-T

93588389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38102888-G-T

http://identifiers.org/hco/10/GRCh38#93588394-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38102891-A-C

93588394-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38102891-A-T

93588425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38103001-T-C

http://identifiers.org/hco/10/GRCh38#93588432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38103016-C-A

http://identifiers.org/hco/10/GRCh38#93588444-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38103028-A-C

93588487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38103066-T-C

93588511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38103088-G-A

93588511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38103088-G-T

93588535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38103109-A-G

93588535-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38103109-A-T

93588553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38103127-A-G

http://identifiers.org/hco/10/GRCh38#93588556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38103130-C-A

93588556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38103130-C-T

93588592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38103165-G-T

93588617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38103192-T-C

93588621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38103196-A-G

93588871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38103260-G-T

93588904-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38103293-T-G

93588957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38103335-A-G

93588957-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38103335-A-T

93588962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38103340-G-T

93588971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38103344-G-A

93588971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38103344-G-T

93588973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38103346-G-A

93589006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38103378-A-G

93589064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38103420-G-T

93589154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38103502-G-A

93589154-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38103502-G-C

93589261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38103583-A-G

93589262-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38103584-G-T

93589296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38103622-A-G

http://identifiers.org/hco/10/GRCh38#93589332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38103651-C-A

93589360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38103679-A-G

93589408-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38103727-T-G

93589425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38103744-A-G

93589532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38103801-C-T

93589567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38103836-G-A

93589567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38103836-G-T

93589588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38103857-G-A

93589588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38103857-G-T

http://identifiers.org/hco/10/GRCh38#93589635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38103888-C-A

93589635-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38103888-C-G

93589635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38103888-C-T

93589680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38103919-G-A

93589680-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38103919-G-T

93589704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38103942-G-A

93589704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38103942-G-T

93589709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38103947-T-C

93589798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38104044-G-A

93590801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38104272-A-G

93590864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38104335-C-T

http://identifiers.org/hco/10/GRCh38#93590891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38104362-C-A

93590891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38104362-C-T

93591174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38104577-A-G

93591177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38104580-T-C

93591307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38104658-A-G

93591465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38104804-G-A

93591651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38104960-T-C

93591680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38104984-T-C

93591700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38105001-G-A

http://identifiers.org/hco/10/GRCh38#93591704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38105005-C-A

http://identifiers.org/hco/10/GRCh38#93591705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38105006-C-A

93591771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38105026-G-A

93591771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38105026-G-T

http://identifiers.org/hco/10/GRCh38#93591773-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38105028-A-C

http://identifiers.org/hco/10/GRCh38#93591786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38105041-C-A

93591786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38105041-C-T

http://identifiers.org/hco/10/GRCh38#93591820-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38105050-C-A

93591820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38105050-C-T

http://identifiers.org/hco/10/GRCh38#93591888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38105118-C-A

93591888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38105118-C-T

93591924-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 38105176-G-C

93591924-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 38105176-G-T

http://identifiers.org/hco/10/GRCh38#93591929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#38105181-C-A

93591929-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 38105181-C-G

93591929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 38105181-C-T

93591951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38105195-T-C

93591951-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38105195-T-G

93592046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38105294-T-C

93592065-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38105310-C-G

93592066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38105311-T-C

93592165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38105415-T-C

93592165-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38105415-T-G

93592166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38105416-G-A

93592166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38105416-G-T

93592182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38105433-A-G

93592183-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38105434-T-A

93592242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38105452-T-C

93592260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38105470-C-T

93593146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38106082-C-T

93593376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38106311-C-T

93593614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38106547-G-A

http://identifiers.org/hco/10/GRCh38#93593713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38106646-C-A

93593713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38106646-C-T

93593781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38106687-G-T

93593833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 38106730-G-A

93593833-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron_variant, missense_variant
orthologous variants: 38106730-G-C

93593851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 38106748-G-A

93593911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 38106808-G-A

93593920-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 38106817-C-G

93593920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 38106817-C-T

93593932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 38106829-G-A

93593947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 38106844-A-G

93593962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 38106859-G-A

93593962-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 38106859-G-C

93593965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 38106862-G-A

93593965-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron_variant, missense_variant
orthologous variants: 38106862-G-T

93593971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 38106868-G-A

93594091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38106965-G-A

93594091-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38106965-G-T

93594142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38107002-G-T

93594183-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38107042-A-T

93594232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38107090-T-C

93594245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38107103-T-C

93594480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38107351-G-A

http://identifiers.org/hco/10/GRCh38#93594527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38107378-C-A

93594527-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38107378-C-G

93594527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38107378-C-T

93594534-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38107386-T-A

93594534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38107386-T-C

93594558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38107431-C-T

93594619-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38107493-G-C

http://identifiers.org/hco/10/GRCh38#93595336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38107998-C-A

93595336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38107998-C-T

93595337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38107999-G-A

93595337-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38107999-G-C

http://identifiers.org/hco/10/GRCh38#93595425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38108084-C-A

93595564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38108212-G-T

93595602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38108249-G-A

93595602-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38108249-G-C

93595669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38108316-G-A

93595669-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38108316-G-C

93595785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38108432-G-A

93595921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38108552-C-T

93596190-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38108934-C-G

93596190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38108934-C-T

93596223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38108957-C-T

93596308-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38109038-G-C

http://identifiers.org/hco/10/GRCh38#93596478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38109206-C-A

93596617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38109324-T-C

93596622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38109329-C-T

93596689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38109394-T-C

93596743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron_variant, undefined
orthologous variants: 38109449-G-A

93596780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38109477-T-C

93596860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38109535-A-G

93596869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38109544-G-T

93597111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38109758-G-A

93597155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38109804-G-T

93597190-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38109838-T-G

93597310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38109966-C-T

93597337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38109991-C-T

93597469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38110123-A-G

93597532-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38110198-C-G

93597547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38110213-G-A

93597812-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38110651-G-C

93598194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38111000-G-A

93598233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38111048-C-T

93598235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38111050-T-C

93599717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38111932-A-G

93599752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38111960-A-G

93599781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38111993-T-C

93599943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38112131-C-T

93600015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38112199-A-G

93600032-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38112216-C-G

93600195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38112342-C-T

93600222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38112355-T-C

93600245-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38112379-C-G

93600245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38112379-C-T

93600269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38112402-G-A

93600269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38112402-G-T

93600288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38112421-G-A

93600288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38112421-G-T

93600291-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38112424-G-C

93600291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38112424-G-T

93600330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38112442-C-T

93600331-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38112443-C-G

93600336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38112448-G-A

93600336-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38112448-G-T

93600341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38112453-G-T

93600342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38112454-G-T

93600573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38112648-C-T

93600585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron_variant, undefined
orthologous variants: 38112660-A-G

93600602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron_variant, undefined
orthologous variants: 38112688-C-T

93600639-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38112717-G-C

93600639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38112717-G-T

93600683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 38112760-G-T

93600717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 38112794-G-A

93600717-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron_variant, missense_variant
orthologous variants: 38112794-G-C

93600717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron_variant, missense_variant
orthologous variants: 38112794-G-T

93600741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 38112818-G-A

http://identifiers.org/hco/10/GRCh38#93600847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38112926-C-A

93600847-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38112926-C-G

93600847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38112926-C-T

93600864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38112941-G-A

93600969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron_variant, splice_region_variant, synonymous_variant
orthologous variants: 38113018-G-A

93600969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron_variant, splice_region_variant, synonymous_variant
orthologous variants: 38113018-G-T

http://identifiers.org/hco/10/GRCh38#93601068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38113116-C-A

93601068-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38113116-C-G

93601068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38113116-C-T

93601116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38113157-C-T

http://identifiers.org/hco/10/GRCh38#93601140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38113173-C-A

93601140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38113173-C-T

http://identifiers.org/hco/10/GRCh38#93601163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#38113198-C-A

93601163-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 38113198-C-G

93601163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 38113198-C-T

93601203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 38113233-G-A

93601203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 38113233-G-T

93601234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 38113264-G-A

93601234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 38113264-G-T

93601242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38113271-G-A

93601242-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38113271-G-C

93601331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron_variant, undefined
orthologous variants: 38113351-G-A

93601487-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 38113539-T-G

93601635-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 38113675-T-A

93601635-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 38113675-T-G

93601688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 38113723-A-G

93602352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38114400-T-C

93602748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38115327-A-G

93602748-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38115327-A-T

93602773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38115360-G-A

93602809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38115395-G-A

93602901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38115458-G-A

93603049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38115587-T-C

93603817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38116404-T-C

93603854-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38116441-T-A

93603921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38116490-C-T

http://identifiers.org/hco/10/GRCh38#93603938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38116507-C-A

93603938-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38116507-C-G

93603938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38116507-C-T

93603964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38116533-G-A

93603972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: intron variant
orthologous variants: 38116541-G-T

93604161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3 prime UTR variant
orthologous variants: 38116753-G-T

93604170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3 prime UTR variant
orthologous variants: 38116762-G-T

93604201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3 prime UTR variant
orthologous variants: 38116785-C-T

http://identifiers.org/hco/10/GRCh38#93604279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38116856-C-A

93604323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3 prime UTR variant
orthologous variants: 38116903-A-G

93604331-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3 prime UTR variant
orthologous variants: 38116911-T-G

93604337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3 prime UTR variant
orthologous variants: 38116917-C-T

http://identifiers.org/hco/10/GRCh38#93604338-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38116918-A-C

93604372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19061
most severe consequence: 3 prime UTR variant
orthologous variants: 38116955-G-T