26826800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 5 prime UTR variant
orthologous variants: 133360703-G-A

26826800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 5 prime UTR variant
orthologous variants: 133360703-G-T

26826856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: missense variant
orthologous variants: 133360647-G-A

26826856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: missense variant
orthologous variants: 133360647-G-T

http://identifiers.org/hco/1/GRCh38#26826877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#133360626-C-A

26826877-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: missense variant
orthologous variants: 133360626-C-G

26826877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: missense variant
orthologous variants: 133360626-C-T

26827027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: missense variant
orthologous variants: 133360500-G-A

26827027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: missense variant
orthologous variants: 133360500-G-T

26827066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: missense variant
orthologous variants: 133360461-G-A

26827066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: missense variant
orthologous variants: 133360461-G-T

http://identifiers.org/hco/1/GRCh38#26827102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#133360425-C-A

26827102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: missense variant
orthologous variants: 133360425-C-T

26827160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133360379-G-A

26827160-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133360379-G-C

26827160-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133360379-G-T

http://identifiers.org/hco/1/GRCh38#26827216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#133360344-C-A

26827216-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133360344-C-G

26827216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133360344-C-T

26827633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133360095-C-T

26828125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133359640-A-G

http://identifiers.org/hco/1/GRCh38#26828195-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#133359545-A-C

26828195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133359545-A-G

26828195-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133359545-A-T

26828203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133359537-C-T

http://identifiers.org/hco/1/GRCh38#26828489-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#133359260-A-C

26828692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133359062-A-G

26828850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133358895-C-T

26829105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133358688-T-C

26829146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133358631-G-A

26829172-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133358589-T-G

26829224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133358534-A-G

26829352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133358386-C-T

26829421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133358305-C-T

26829709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133358092-A-G

26829900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133357950-C-T

26830040-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133357833-A-T

26832277-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133355003-A-T

26832284-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133354997-A-T

26832499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 133354617-A-G

26832499-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 133354617-A-T

26832589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: missense variant
orthologous variants: 133354527-G-A

26832589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: missense variant
orthologous variants: 133354527-G-T

26832641-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133354483-C-G

26832753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133354388-A-G

26832753-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133354388-A-T

26832837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133354327-G-A

26832919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133354250-A-G

26832919-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133354250-A-T

26833007-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133353977-C-G

http://identifiers.org/hco/1/GRCh38#26833139-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#133353694-A-C

26833187-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133353636-G-C

26833647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133353338-C-T

26833831-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133353151-C-G

26834060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133352956-G-A

26834060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133352956-G-T

26834169-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133352871-C-G

26834292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133352753-A-G

26834298-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133352747-A-T

26834528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133352420-C-T

http://identifiers.org/hco/1/GRCh38#26834718-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#133352224-A-C

26834825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133352124-T-C

26834825-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133352124-T-G

26834935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133352043-G-T

26834939-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133352039-T-G

26834992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133351989-G-A

26835001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133351980-C-T

26835132-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133351864-T-G

26835232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133351787-C-T

26838303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133348934-T-C

26838322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133348915-G-A

26838366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133348874-C-T

26838412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133348809-G-T

26838429-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133348792-C-G

26838493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133348776-T-C

26838953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron_variant, undefined
orthologous variants: 133348365-C-T

26838956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron_variant, undefined
orthologous variants: 133348362-G-A

26839010-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron_variant, undefined
orthologous variants: 133348308-G-C

26839074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron_variant, undefined
orthologous variants: 133348226-T-C

26839119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron_variant, undefined
orthologous variants: 133348174-C-T

26839268-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133347997-T-A

http://identifiers.org/hco/1/GRCh38#26839285-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#133347980-A-C

26839474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133347546-G-A

26839809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133347275-G-A

26839925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133347241-G-A

26840097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133347128-T-C

26840225-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133346997-T-A

26840629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133346523-A-G

26841028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133346139-G-A

26841192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133345877-C-T

26841297-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133345770-A-T

26841314-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133345694-T-G

26841376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133345634-C-T

26841401-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133345610-T-A

26841447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133345570-A-G

26841468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133345551-A-G

26841555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133345471-T-C

26841557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133345469-T-C

26841572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133345455-G-A

26841572-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133345455-G-C

26841702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133345337-T-C

26841740-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133345304-C-G

26842514-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133344220-C-G

26848345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133342900-T-C

26848406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133342845-G-A

26848456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133342777-G-T

26848467-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133342766-T-G

26848547-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133342691-T-A

26848547-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133342691-T-G

26848673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: missense variant
orthologous variants: 133342573-A-G

26848673-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: missense variant
orthologous variants: 133342573-A-T

26848694-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: missense variant
orthologous variants: 133342552-T-G

26848742-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: missense variant
orthologous variants: 133342504-T-A

26848792-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133342463-T-A

26848793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133342462-C-T

26848820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133342439-G-A

26848820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133342439-G-T

26848846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133342414-G-T

26848867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133342393-G-A

26848867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133342393-G-T

26848997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133342325-G-A

http://identifiers.org/hco/1/GRCh38#26849381-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#133342007-A-C

26849382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron_variant, undefined
orthologous variants: 133342006-G-A

26849382-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron_variant, undefined
orthologous variants: 133342006-G-C

26849526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133341881-C-T

26849651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron_variant, undefined
orthologous variants: 133341760-C-T

26850039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133341483-G-A

26850351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: missense variant
orthologous variants: 133341197-A-G

26850420-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: missense variant
orthologous variants: 133341128-G-C

26850616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133340938-G-A

http://identifiers.org/hco/1/GRCh38#26850750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#133340829-C-A

26850750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133340829-C-T

26850802-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133340757-C-G

26851098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133340362-T-C

http://identifiers.org/hco/1/GRCh38#26851101-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#133340356-A-C

http://identifiers.org/hco/1/GRCh38#26851103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#133340354-C-A

26851103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133340354-C-T

26851240-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133340223-A-T

http://identifiers.org/hco/1/GRCh38#26851290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#133340211-C-A

http://identifiers.org/hco/1/GRCh38#26851299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#133340203-C-A

26851299-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133340203-C-G

26851299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133340203-C-T

26852021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133338897-A-G

26852237-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133338713-T-G

26852619-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133338034-A-T

26852661-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133338014-G-T

26852840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 133337704-G-A

26852840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 133337704-G-T

26852874-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 133337673-G-C

26852907-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 133337641-C-G

26852907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 133337641-C-T

http://identifiers.org/hco/1/GRCh38#26852913-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#133337635-A-C

26852913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 133337635-A-G

26852913-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 133337635-A-T

26852919-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 133337623-C-G

26852959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 133337588-T-C

26852959-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 133337588-T-G

http://identifiers.org/hco/1/GRCh38#26853012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#133337534-C-A

26853012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 133337534-C-T

26853072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 133337466-C-T

26853109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 133337362-T-C

http://identifiers.org/hco/1/GRCh38#26853157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#133337311-C-A

26853157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 133337311-C-T

http://identifiers.org/hco/1/GRCh38#26853260-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#133337242-A-C

26853260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133337242-A-G

26853260-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133337242-A-T

http://identifiers.org/hco/1/GRCh38#26853271-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#133337231-A-C

26853271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron_variant, undefined
orthologous variants: 133337231-A-G

http://identifiers.org/hco/1/GRCh38#26853661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#133336139-C-A

26853661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: intron variant
orthologous variants: 133336139-C-T

26853762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: synonymous variant
orthologous variants: 133336046-C-T

26853778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: missense variant
orthologous variants: 133336030-A-G

26853867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133335949-G-A

26854173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133335655-G-A

26854173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133335655-G-T

26854264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133335583-G-A

26854381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133335484-A-G

26854381-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133335484-A-T

26854384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133335481-T-C

http://identifiers.org/hco/1/GRCh38#26854388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#133335477-C-A

26854533-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133335344-A-T

http://identifiers.org/hco/1/GRCh38#26854592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#133335284-C-A

26854639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133335238-G-T

http://identifiers.org/hco/1/GRCh38#26854809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#133335079-C-A

http://identifiers.org/hco/1/GRCh38#26854824-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#133335067-C-A

26854824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133335067-C-T

http://identifiers.org/hco/1/GRCh38#26854848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#133335048-C-A

26854848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133335048-C-T

26854869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133335027-G-T

26854871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133335025-G-A

26854871-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133335025-G-C

26854871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133335025-G-T

http://identifiers.org/hco/1/GRCh38#26854902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#133334991-C-A

26854902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133334991-C-T

26854940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133334954-G-T

26854966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133334927-G-A

26854966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133334927-G-T

http://identifiers.org/hco/1/GRCh38#26854971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#133334922-C-A

26854971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133334922-C-T

http://identifiers.org/hco/1/GRCh38#26854984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#133334907-C-A

26854984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133334907-C-T

26855111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133334854-G-T

26855118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133334847-T-C

26855159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133334806-G-T

26855254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133334709-A-G

26855259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133334704-A-G

26855316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133334663-G-A

26855316-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133334663-G-C

26855316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133334663-G-T

http://identifiers.org/hco/1/GRCh38#26855319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#133334660-C-A

26855319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133334660-C-T

26855321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133334658-A-G

26855329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133334650-A-G

26855340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133334639-G-A

26855340-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133334639-G-T

26855586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133334429-G-T

26855634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133334380-G-T

26855758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133334265-G-T

26855763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133334260-G-T

26855917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133334122-G-A

http://identifiers.org/hco/1/GRCh38#26856154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#133333920-C-A

http://identifiers.org/hco/1/GRCh38#26856304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#133333770-C-A

http://identifiers.org/hco/1/GRCh38#26856415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#133333661-C-A

26856535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133333566-G-A

26856535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133333566-G-T

26856575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133333531-G-A

26856575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133333531-G-T

26856579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133333527-G-A

26856579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133333527-G-T

26856642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133333502-T-C

26856710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133333455-G-A

http://identifiers.org/hco/1/GRCh38#26856725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#133333440-C-A

26856725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133333440-C-T

26856795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133333374-G-A

26856795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133333374-G-T

http://identifiers.org/hco/1/GRCh38#26856834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#133333335-C-A

26856834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133333335-C-T

26856852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3 prime UTR variant
orthologous variants: 133333317-T-C

http://identifiers.org/hco/1/GRCh38#26856925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#133333244-C-A

26856925-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3 prime UTR variant
orthologous variants: 133333244-C-G

26856925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3 prime UTR variant
orthologous variants: 133333244-C-T

26857038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3 prime UTR variant
orthologous variants: 133333120-G-T

26857134-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3 prime UTR variant
orthologous variants: 133333025-T-A

26857134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3 prime UTR variant
orthologous variants: 133333025-T-C

26857134-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3 prime UTR variant
orthologous variants: 133333025-T-G

26857138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3 prime UTR variant
orthologous variants: 133333021-C-T

26857273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3 prime UTR variant
orthologous variants: 133332893-T-C

http://identifiers.org/hco/1/GRCh38#26857428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#133332771-C-A

26857428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3 prime UTR variant
orthologous variants: 133332771-C-T

26857516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3 prime UTR variant
orthologous variants: 133332692-T-C

26857529-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3 prime UTR variant
orthologous variants: 133332680-G-T

26857567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3 prime UTR variant
orthologous variants: 133332648-T-C

26857589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20712
most severe consequence: 3 prime UTR variant
orthologous variants: 133332622-T-C