11257962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66402356-A-G

http://identifiers.org/hco/17/GRCh38#11258078-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66402234-A-C

11258449-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66401902-G-C

11258918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66401123-A-G

11258920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66401121-T-C

http://identifiers.org/hco/17/GRCh38#11259173-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66400856-A-C

11259192-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66400851-G-C

11259789-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66399470-G-C

11259873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66399403-C-T

11260087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66399197-A-G

11260231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66399067-A-G

11260323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66398978-C-T

11260413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66398910-A-G

http://identifiers.org/hco/17/GRCh38#11260681-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66398543-A-C

11260681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66398543-A-G

11260776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66398456-C-T

11260783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66398449-C-T

11260798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66398434-C-T

11260941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66398249-A-G

11261191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66397987-G-A

11261263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66397942-G-A

11261316-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66397882-T-A

11261451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66397774-G-A

11262263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66394726-G-A

11262294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66394696-G-T

11262335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66394631-A-G

11262353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66394613-G-A

11262367-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66394600-T-A

11262367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66394600-T-C

11262406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66394565-T-C

11262484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66394457-G-A

11262500-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66394441-A-T

11262582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66394361-A-G

11262689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66394277-G-A

11262777-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66394214-C-G

11262871-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66394117-C-G

11263006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66393972-G-A

11263047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66393939-C-T

11263126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66393860-A-G

11263144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66393840-G-A

http://identifiers.org/hco/17/GRCh38#11263200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66393806-C-A

11263200-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66393806-C-G

11263253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66393745-T-C

http://identifiers.org/hco/17/GRCh38#11263302-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66393696-A-C

11263302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66393696-A-G

11263319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66393680-G-A

11263319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66393680-G-T

11263463-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: missense variant
orthologous variants: 66393539-A-T

11263520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: missense variant
orthologous variants: 66393482-A-G

11263535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66393467-C-T

11263574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66393428-G-T

http://identifiers.org/hco/17/GRCh38#11263602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66393399-C-A

11263602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66393399-C-T

http://identifiers.org/hco/17/GRCh38#11263614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66393387-C-A

11263694-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66393312-G-C

11263776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66393246-G-A

11263830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66393192-C-T

11263847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66393175-G-A

11263904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66393118-C-T

11263964-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66393073-T-G

11264012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66393024-T-C

11264179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66392516-T-C

11264631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron_variant, undefined
orthologous variants: 66392038-A-G

11264759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66391930-C-T

11265005-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66391690-T-A

11265052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66391641-G-A

11265087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66391607-A-G

11265158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66391538-C-T

11265239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66391464-G-A

11265451-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66390535-C-G

11265721-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66390316-C-G

11265971-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66390090-T-G

11265981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66390066-G-T

11266085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66389971-A-G

11266099-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66389957-A-T

11266301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66389770-T-C

11266357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66389702-G-A

11266416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66389647-T-C

11266514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66389545-A-G

11269395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66388597-C-T

11269436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66388558-G-A

11269487-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66388508-C-G

http://identifiers.org/hco/17/GRCh38#11269537-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66388477-A-C

11269544-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66388474-C-G

11269960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66388070-A-G

11272097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66387777-C-T

11272135-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66387731-T-G

11272531-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66387406-T-A

11272564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66387369-T-C

11272619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66387334-G-T

11272680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66387290-C-T

11272853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66387147-C-T

11273191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66386901-C-T

11273244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66386844-C-T

11273251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66386837-C-T

11273987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66385497-T-C

11274036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66385449-T-C

11274191-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66385302-A-T

11274312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66385196-C-T

11274554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66384617-T-C

11275078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66384100-A-G

11275300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66383924-G-A

11275300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66383924-G-T

11275509-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66383734-C-G

11275509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66383734-C-T

11275844-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66383467-T-G

11276754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66382972-C-T

http://identifiers.org/hco/17/GRCh38#11276767-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66382958-A-C

11276904-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66382819-A-T

11276910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66382810-G-A

http://identifiers.org/hco/17/GRCh38#11277040-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66382680-A-C

http://identifiers.org/hco/17/GRCh38#11277080-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66382640-A-C

http://identifiers.org/hco/17/GRCh38#11277321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66382533-C-A

11277321-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66382533-C-G

11277359-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66382494-T-G

11277382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66382471-A-G

11277529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66382308-A-G

11277606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66382231-A-G

11278152-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66381210-T-G

11278561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66380647-A-G

11278692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66380537-A-G

11278830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66380402-G-T

11278900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66380334-G-A

http://identifiers.org/hco/17/GRCh38#11278940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66380294-C-A

11279146-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66380098-C-G

11279183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66380079-G-T

11279466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66379862-G-A

11279489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66379850-A-G

11279625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66379758-A-G

11279779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66379568-A-G

11279846-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66379519-G-C

http://identifiers.org/hco/17/GRCh38#11280002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66379398-C-A

11280002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66379398-C-T

11280057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66379368-A-G

11280061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66379364-G-A

11280389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66379021-T-C

11280483-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66378910-C-G

11280498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66378892-G-A

11280498-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66378892-G-C

11280498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66378892-G-T

11280674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66378712-A-G

http://identifiers.org/hco/17/GRCh38#11280818-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66378570-A-C

11281071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66378336-T-C

11281071-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66378336-T-G

11281214-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66378202-G-C

http://identifiers.org/hco/17/GRCh38#11281228-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66378188-A-C

11281657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66377757-A-G

http://identifiers.org/hco/17/GRCh38#11281900-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66377531-A-C

11283140-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66377392-C-G

11283140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66377392-C-T

11283195-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66377340-T-A

11283205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66377330-A-G

11283306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66377237-C-T

11283590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66376963-G-A

11283593-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66376960-G-C

11283622-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66376935-T-A

11283776-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66376789-C-G

11283787-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66376778-A-T

11283919-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66376641-C-G

http://identifiers.org/hco/17/GRCh38#11284105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66376368-C-A

11284105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66376368-C-T

11284290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66376194-A-G

11284545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66375952-T-C

11284955-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66374822-T-G

11285021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66374751-C-T

11285287-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66374515-G-C

11285665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66374171-G-A

11285665-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66374171-G-C

11285705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66374118-G-A

11285721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66374102-A-G

11285853-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66373996-T-A

11285897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66373964-C-T

11286264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66373761-C-T

11286876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66373169-A-G

11287004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66373044-G-A

11296679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66351056-G-A

11296752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66350983-G-A

11296804-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66350953-A-T

11297430-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66350240-C-G

11297990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66349691-G-A

11298215-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66349470-A-T

11298417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66349297-A-G

11298420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66349294-G-T

11298742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66348982-A-G

11298855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66348873-G-A

11299635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66348191-A-G

11300287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66347767-C-T

11300493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66347661-G-A

11300508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66347651-G-A

11300508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66347651-G-T

11300555-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66347605-A-T

11300629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66347558-G-A

11300802-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66347474-T-A

11300807-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66347469-G-C

http://identifiers.org/hco/17/GRCh38#11300882-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66347386-A-C

11300882-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66347386-A-T

11300885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66347383-T-C

11301304-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66346984-C-G

11301309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66346979-T-C

http://identifiers.org/hco/17/GRCh38#11301320-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66346974-A-C

11301320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66346974-A-G

11301410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66346881-C-T

11301414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66346877-G-A

11301551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66346742-G-A

11301739-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66346557-A-T

11302285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66346244-G-A

11302570-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66345993-G-C

11302570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66345993-G-T

11304026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66342898-T-C

11304154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66342780-C-T

11304772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66342255-G-A

11304797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66342233-C-T

http://identifiers.org/hco/17/GRCh38#11304816-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66342214-A-C

11305176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66341861-G-T

11305379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66341663-A-G

11305468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66341535-C-T

11305470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66341533-C-T

11305754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66341174-C-T

11305910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66341106-G-A

11305936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66341080-C-T

11305937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66341079-T-C

11305937-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66341079-T-G

11306210-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66340933-C-G

http://identifiers.org/hco/17/GRCh38#11306343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66340801-C-A

11306678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66340487-G-A

11306809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66340365-C-T

http://identifiers.org/hco/17/GRCh38#11306847-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66340325-A-C

11306870-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66340301-G-C

11306941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66340245-T-C

11306943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66340243-G-A

11306997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66340157-G-T

http://identifiers.org/hco/17/GRCh38#11307205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66340049-C-A

11307228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66340032-G-A

11307779-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66339540-T-A

11307779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66339540-T-C

11308005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66339368-G-A

11308042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66339331-C-T

11308175-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66339197-G-T

11308333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66339045-C-T

11308361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66339018-G-T

11308390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66338989-G-A

11308422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66338960-A-G

11308519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66338865-A-G

11309278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron_variant, undefined
orthologous variants: 66338414-G-A

11309306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron_variant, undefined
orthologous variants: 66338386-T-C

11309380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron_variant, undefined
orthologous variants: 66338314-C-T

11309430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron_variant, undefined
orthologous variants: 66338269-A-G

11309487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron_variant, undefined
orthologous variants: 66338211-C-T

11309521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron_variant, undefined
orthologous variants: 66338171-C-T

11309909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron_variant, undefined
orthologous variants: 66337758-G-A

11312265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron_variant, undefined
orthologous variants: 66335842-G-T

11312734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66335403-T-C

11313201-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66334974-C-G

http://identifiers.org/hco/17/GRCh38#11313212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66334963-C-A

11313269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66334911-T-C

11313745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66334505-G-A

11313765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66334486-T-C

11314508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66333849-G-A

11315181-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66333528-C-G

11315259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66333462-G-A

11315475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66333259-T-C

11315746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66332997-A-G

11315746-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66332997-A-T

11315880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66332822-G-T

11315938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66332758-T-C

11316169-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66332529-A-T

http://identifiers.org/hco/17/GRCh38#11316353-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66332424-A-C

11316353-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66332424-A-T

11316355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66332422-T-C

11316356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66332421-G-T

11316469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66332375-G-A

11316738-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66332271-A-T

11316756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66332249-T-C

11317040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66331974-G-A

11317400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66331616-T-C

11319398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66327600-G-A

11319398-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66327600-G-C

11320048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66326866-T-C

11320066-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66326848-A-T

11321167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66326436-A-G

http://identifiers.org/hco/17/GRCh38#11321518-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66326095-A-C

11321518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66326095-A-G

11322605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66322272-T-C

11322654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66322224-A-G

http://identifiers.org/hco/17/GRCh38#11322937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66318284-C-A

11323848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66317429-A-G

11323917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66317362-T-C

11324249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66317040-G-A

11324418-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66316882-T-A

11324572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66316751-T-C

11324645-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66316690-C-G

11324831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66316482-G-A

11324900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66316413-C-T

11325209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66316110-G-A

11325375-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66315942-C-G

11325375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66315942-C-T

11325460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66315857-G-T

11325586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66315727-T-C

11326522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66315114-T-C

11326533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66315094-G-A

11326689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66314976-T-C

11326716-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66314951-T-A

11326896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66314771-A-G

11328537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66313446-A-G

11328843-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66313170-C-G

11328843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66313170-C-T

11329055-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66312976-C-G

11329055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66312976-C-T

11329105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66312930-T-C

11329416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66312632-C-T

11329482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66312581-C-T

11329531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66312536-A-G

11329627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66312457-T-C

11329870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66312206-A-G

11330442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66311334-G-A

http://identifiers.org/hco/17/GRCh38#11330543-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66311247-A-C

11330543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66311247-A-G

http://identifiers.org/hco/17/GRCh38#11330915-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66310753-A-C

11330916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66310752-C-T

11331129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66310551-G-A

11331157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66310525-C-T

11331296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66310386-C-T

11331444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66310230-A-G

11331853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66309849-T-C

11331954-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66309766-A-T

11332107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66309616-C-T

11332230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66309492-C-T

11332561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66309166-G-A

11332874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66308881-C-T

11333483-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66308435-C-G

11333493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66308425-C-T

11333914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66308127-G-A

11333914-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66308127-G-C

11334385-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66307516-G-C

http://identifiers.org/hco/17/GRCh38#11334390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66307511-C-A

11334440-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66307463-C-G

http://identifiers.org/hco/17/GRCh38#11334535-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66307375-A-C

11335080-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66307076-T-A

11335091-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66307065-T-A

11335091-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66307065-T-G

11335123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66307033-G-T

11335667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66306397-A-G

11335679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66306385-T-C

11335864-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66306213-T-G

11335887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66306190-G-A

11335887-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66306190-G-C

11336248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66306168-G-A

11336333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66306088-A-G

11336356-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66306066-G-C

11336551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66305878-A-G

http://identifiers.org/hco/17/GRCh38#11336552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66305877-C-A

11336552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66305877-C-T

11336893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66305553-C-T

11337257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66305196-G-A

11337308-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66305152-A-T

11337521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66304931-C-T

11338235-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66303125-C-G

11339271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66303979-A-G

11339493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66303768-G-A

11339668-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66303609-C-G

11339754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66303534-G-A

11339880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66303431-G-A

11339924-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66303393-G-C

11340494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66302692-C-T

11340718-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66302490-A-T

11341145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66302067-G-A

11341270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66301950-C-T

http://identifiers.org/hco/17/GRCh38#11347190-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66297720-A-C

11347190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66297720-A-G

11347317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66297614-A-G

11347345-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66297585-G-C

http://identifiers.org/hco/17/GRCh38#11347493-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66297423-A-C

11347493-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66297423-A-T

11347642-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66297289-T-G

11347835-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66297099-G-C

http://identifiers.org/hco/17/GRCh38#11347885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66297048-C-A

11347885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66297048-C-T

11347903-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66297030-A-T

11347907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66297026-G-A

11347907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66297026-G-T

11347953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66296981-A-G

11348064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66296852-T-C

11348662-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66296204-T-G

11348708-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66296164-C-G

11349006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66295870-G-A

11349157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66295727-G-A

11349310-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66295583-G-T

11349593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66295269-C-T

11353644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66292014-G-A

11353909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66291754-G-A

11353986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66291686-G-T

11353998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66291673-G-T

http://identifiers.org/hco/17/GRCh38#11354052-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66291620-A-C

11354052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66291620-A-G

11354124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66291545-G-A

11354141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66291528-C-T

11354235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66291434-G-A

11354513-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66291214-T-G

11354528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66291198-T-C

11355095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66290632-G-A

11355110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66290617-C-T

11355181-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66290546-G-C

11355591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66289690-A-G

11356084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66289252-G-A

11356099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66289236-T-C

http://identifiers.org/hco/17/GRCh38#11356183-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66289135-A-C

11356360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66288981-A-G

11356361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66288980-T-C

11356603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66288729-C-T

11357426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66288227-A-G

11357523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66288157-T-C

11357767-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66287914-T-G

11357850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66287818-G-A

11358172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66287523-T-C

11358357-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66287342-G-C

11368108-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66279764-A-T

11368125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66279747-C-T

http://identifiers.org/hco/17/GRCh38#11368132-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66279740-A-C

http://identifiers.org/hco/17/GRCh38#11368206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66279684-C-A

11368206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66279684-C-T

11368217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66279673-G-T

11368568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66279385-A-G

11368975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66279322-G-A

http://identifiers.org/hco/17/GRCh38#11369343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66278974-C-A

11369536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66278808-C-T

http://identifiers.org/hco/17/GRCh38#11369552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66278793-C-A

11369552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66278793-C-T

11369611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66278734-T-C

11369990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66278337-C-T

11370272-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66277821-T-A

11370383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66277688-G-A

11370685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66277427-T-C

11371237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66276958-G-A

http://identifiers.org/hco/17/GRCh38#11371713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66276540-C-A

11371739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66276514-A-G

11371940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66276330-A-G

11372026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66276248-T-C

11372092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66276151-C-T

11373128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66274951-A-G

11373383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66274696-A-G

11373534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66273838-A-G

11373588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66273780-G-A

11373588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66273780-G-T

11373625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66273743-T-C

http://identifiers.org/hco/17/GRCh38#11373796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66273567-C-A

11373898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66273460-G-T

11374149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66273228-T-C

11374247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66273130-T-C

11374303-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66273075-T-A

11374303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66273075-T-C

11374514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66272871-G-A

11374579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66272805-C-T

11375032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66272284-C-T

11375037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66272279-T-C

11375094-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66272225-T-A

11375458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66271526-T-C

11375546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66271446-C-T

11375598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66271395-C-T

11375641-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66271353-C-G

11375975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66271031-G-A

11376063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66270942-T-C

11376278-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66270721-C-G

11376305-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66270692-C-G

11377215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66269710-T-C

11377421-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66268596-T-G

11377466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66268595-C-T

11377556-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66268531-G-C

http://identifiers.org/hco/17/GRCh38#11377657-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66268431-A-C

11378120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66268149-A-G

http://identifiers.org/hco/17/GRCh38#11378226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66268049-C-A

11378226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66268049-C-T

11378270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66268006-C-T

11378424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66267932-A-G

11378585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66267760-A-G

11378585-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66267760-A-T

11378605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66267741-T-C

11378800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66267545-T-C

11378865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66267479-G-A

11379196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66266284-A-G

11379228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66266252-A-G

11379289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66266202-A-G

http://identifiers.org/hco/17/GRCh38#11379560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66265932-C-A

11379560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 66265932-C-T

11379580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 66265911-G-A

11379580-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 66265911-G-C

11379580-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 66265911-G-T

11379591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 66265900-A-G

11379637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 66265853-T-C

11379833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 66265674-G-T

http://identifiers.org/hco/17/GRCh38#11379924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66265585-C-A

11379924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 66265585-C-T

11379993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 66265517-A-G

11380051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 66265460-C-T

11380092-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 66265419-T-A

11380224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 66265302-T-C

http://identifiers.org/hco/17/GRCh38#11380582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66264965-C-A

11380582-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66264965-C-G

11380598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66264952-C-T

11380639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66264912-T-C

11380649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66264903-T-C

11380731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66264822-T-C

11380968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66264583-G-T

11381216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66264322-T-C

11387300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66263771-G-A

11387300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66263771-G-T

11387836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66263204-C-T

11387880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66263157-C-T

http://identifiers.org/hco/17/GRCh38#11387886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66263151-C-A

11387909-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66263119-G-C

11387909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66263119-G-T

http://identifiers.org/hco/17/GRCh38#11387933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66263095-C-A

11387933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66263095-C-T

11387937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66263091-T-C

11388028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66263006-G-A

11388028-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66263006-G-C

11388095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66262959-G-A

11388142-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66262913-C-G

11388278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66262781-C-T

11388404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66262650-A-G

11388648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66262425-G-A

11388715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66262363-T-C

11388821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66262304-T-C

11388842-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66262283-T-A

11388842-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66262283-T-G

11388848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66262277-A-G

11389552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66261064-G-T

11389553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66261063-T-C

http://identifiers.org/hco/17/GRCh38#11390508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66260144-C-A

11390508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66260144-C-T

http://identifiers.org/hco/17/GRCh38#11390549-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66260113-A-C

http://identifiers.org/hco/17/GRCh38#11390816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66259838-C-A

11390816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66259838-C-T

11390906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66259750-G-A

11391073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66259593-G-A

11391177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66259492-G-T

11391181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66259488-G-A

11391204-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66259465-A-T

11391442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66258982-T-C

11391587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66258852-G-A

11391587-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66258852-G-C

11391696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66258739-G-A

http://identifiers.org/hco/17/GRCh38#11391896-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66258570-C-A

11392134-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66258352-A-T

11392287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66258203-C-T

11400560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66254809-G-T

11400576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66254793-C-T

11400724-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66254661-A-T

11400762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66254619-C-T

11400856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66254534-C-T

11400929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66254454-G-A

11401592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66254118-G-A

11401613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66254101-A-G

11402248-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66253062-C-G

11402392-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66252917-T-G

http://identifiers.org/hco/17/GRCh38#11402488-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66252849-A-C

11402728-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66252641-A-T

http://identifiers.org/hco/17/GRCh38#11402837-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66252510-A-C

11402917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66252438-A-G

11403087-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66252299-A-T

11403217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66252171-A-G

11403511-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66251901-T-G

11403528-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66251884-C-G

11403733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66251650-C-T

11403927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66251449-G-A

11404214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66251143-A-G

11405891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66249177-C-T

http://identifiers.org/hco/17/GRCh38#11406191-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66248893-A-C

11406221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66248863-C-T

11406658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66248460-A-G

11406942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66248181-G-A

11407117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66248016-A-G

11407192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66247947-A-G

11407252-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66247883-G-C

11407274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66247869-G-T

11407582-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66247492-T-A

11407765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66247307-G-A

11407765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66247307-G-T

11407833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66247244-G-A

http://identifiers.org/hco/17/GRCh38#11407951-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66247138-A-C

11408005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66247085-A-G

11408046-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66247041-C-G

11408046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66247041-C-T

http://identifiers.org/hco/17/GRCh38#11408081-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66247006-A-C

11408241-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66246600-A-T

11408383-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66242439-C-G

11408383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66242439-C-T

11409347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66240632-T-C

11409347-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66240632-T-G

11409972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66240335-A-G

http://identifiers.org/hco/17/GRCh38#11411741-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66239753-A-C

11411809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66239693-T-C

11412158-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66239336-G-C

11412601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66238959-G-A

11412601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66238959-G-T

11412804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66238913-C-T

11413188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66236955-C-T

11413199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66236944-G-A

11413256-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66236891-C-G

11413256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66236891-C-T

11413257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66236890-G-A

11413409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66236734-G-A

11413409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66236734-G-T

11413886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66236317-C-T

11413973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66236254-G-A

11414065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66236180-C-T

11414222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66236039-T-C

11414568-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66235679-T-G

11414704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66235543-A-G

11415665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66234919-C-T

11415678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66234900-A-G

11415696-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66234882-T-G

11415857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66234720-G-A

11416744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66232992-T-C

11418706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66230288-G-A

11418757-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66230239-C-G

11418795-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66230201-T-G

11419471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66229917-T-C

11419540-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66229835-G-C

11420502-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66229014-C-G

11420502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66229014-C-T

http://identifiers.org/hco/17/GRCh38#11420522-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66228994-A-C

11420693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66228857-C-T

11420807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66228757-T-C

11421352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66228161-A-G

11421525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66227979-C-T

http://identifiers.org/hco/17/GRCh38#11423870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66226593-C-A

http://identifiers.org/hco/17/GRCh38#11423952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66226516-C-A

11424099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66226378-G-A

11424099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66226378-G-T

11424131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66226350-T-C

11424162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66226325-T-C

11424518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66225957-T-C

11424531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66225944-T-C

11424548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66225927-G-T

11424576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66225898-G-T

11424584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66225890-G-A

11424584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66225890-G-T

11424633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66225845-T-C

11425032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66225735-G-A

11425032-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66225735-G-T

11425184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66225582-A-G

http://identifiers.org/hco/17/GRCh38#11425518-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66225288-A-C

11425631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66223283-A-G

11425678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66223236-C-T

11425748-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66223164-T-A

11426033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66222599-A-G

11426284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66222355-C-T

11426750-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66221904-C-G

11426779-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66221875-C-G

11426779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66221875-C-T

11426939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66221751-C-T

11427034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66221661-C-T

11427531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66221490-A-G

11427567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66221454-T-C

11427790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66221214-G-A

11427960-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66221088-T-G

11427989-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66221060-G-C

11428084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66220979-C-T

11428196-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66220853-G-C

11428508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66220569-G-T

11428607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66220464-A-G

11429568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66219912-G-A

http://identifiers.org/hco/17/GRCh38#11429583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66219901-C-A

11429583-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66219901-C-G

11429583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66219901-C-T

11430577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66219102-G-A

http://identifiers.org/hco/17/GRCh38#11430810-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66218903-A-C

11430810-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66218903-A-T

http://identifiers.org/hco/17/GRCh38#11430915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66218810-C-A

11430915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66218810-C-T

11431103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66218633-C-T

11431365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66218424-T-C

11431401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66218403-G-T

11431426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66218378-G-T

11431680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66218138-C-T

11431881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66217949-G-T

11432298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66217553-G-A

11432822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66217065-T-C

11432922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66216969-T-C

http://identifiers.org/hco/17/GRCh38#11433053-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66216847-A-C

11433070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66216829-A-G

11433070-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66216829-A-T

11434502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66214602-G-A

http://identifiers.org/hco/17/GRCh38#11434980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66214164-C-A

11436395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66213804-T-C

11436628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66213605-C-T

11436650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66213577-G-A

http://identifiers.org/hco/17/GRCh38#11436728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66213506-C-A

11437164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66213159-T-C

11437535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66212874-C-T

11438822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66212758-C-T

11438881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66212700-C-T

11439137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66212576-C-T

11439269-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66212457-G-C

11439285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66212441-T-C

11439338-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66212396-G-C

11439459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66212249-G-A

11439519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66212201-G-T

http://identifiers.org/hco/17/GRCh38#11439723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66211929-C-A

11440309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66211525-T-C

11440385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66211462-C-T

11440718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66211310-T-C

http://identifiers.org/hco/17/GRCh38#11440753-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66211278-C-A

11440899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66211142-G-T

11441004-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66211052-G-C

11441147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66210938-A-G

11441302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66210799-G-A

11441302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66210799-G-T

11441624-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66210453-T-A

11442077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66210023-T-C

11442108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66209989-G-T

11442110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66209987-C-T

11442607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66209389-T-C

11442673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66209332-T-C

11442828-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66209211-T-G

11442956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66209105-G-A

11443045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66209008-T-C

11443045-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66209008-T-G

http://identifiers.org/hco/17/GRCh38#11443071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66208982-C-A

11443796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66208612-T-C

11443933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66208480-T-C

11444006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66208418-T-C

11445298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66206100-T-C

11446513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66204665-A-G

11446726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66204482-G-A

11446767-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66204438-T-A

11447176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66204032-A-G

11447235-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66203975-T-G

11447703-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66203533-G-C

11447891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66203353-T-C

11447911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66203333-G-A

11448079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66203195-C-T

11448208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66203101-G-A

http://identifiers.org/hco/17/GRCh38#11452191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66200569-C-A

http://identifiers.org/hco/17/GRCh38#11452286-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66200457-C-A

11452568-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66200182-C-G

11452568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66200182-C-T

11452925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66199021-T-C

11452925-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66199021-T-G

11452953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66198993-T-C

11453040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66198900-C-T

11453205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66198735-A-G

11453687-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66198611-T-A

11454024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66198279-A-G

11454038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66198265-T-C

11454066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66198237-C-T

11454363-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66197973-C-G

11454372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66197966-C-T

11454981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66197389-A-G

11455270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66197217-A-G

11455430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66197153-G-A

11455489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66197094-T-C

11455601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66197026-G-A

11455683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66196953-C-T

11455894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66196805-C-T

11456187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66196451-G-A

11456187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66196451-G-T

11456356-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66196279-T-G

11456469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66196159-G-T

11456753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66195897-A-G

11457114-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66195553-T-G

11457204-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66195436-T-A

11457242-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66195377-A-T

11457441-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66195160-G-C

11458328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66193897-G-A

11458378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66193851-C-T

11458603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66193600-G-A

11458642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66193552-T-C

11458782-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66193418-T-A

11459245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66193306-G-T

11459289-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66193263-T-A

11459474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66193111-G-A

11459575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66193031-C-T

11459644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66192966-C-T

11459948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66192673-A-G

11459964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66192657-C-T

11460212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66192410-T-C

11460257-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66192366-C-G

11460286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66192338-T-C

11460723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66192203-C-T

11461346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66191573-G-A

11461371-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66191551-T-G

11461421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66191494-G-A

11461421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66191494-G-T

11461693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66191240-T-C

http://identifiers.org/hco/17/GRCh38#11461734-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66191200-A-C

11461948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66191130-T-C

http://identifiers.org/hco/17/GRCh38#11462055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66191086-C-A

11462417-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66190802-C-G

11462417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66190802-C-T

11464477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66185796-G-A

http://identifiers.org/hco/17/GRCh38#11464954-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66185612-A-C

11464973-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66185594-G-C

11465595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66184817-A-G

11465603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66184809-C-T

http://identifiers.org/hco/17/GRCh38#11465608-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66184791-A-C

11465850-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66184503-C-G

11466021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66184302-G-T

http://identifiers.org/hco/17/GRCh38#11466522-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66182614-A-C

11466583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66182556-C-T

11466652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66182435-C-T

11466692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66182381-T-C

11466723-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66182345-A-T

11467085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66182034-A-G

11467264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66181495-A-G

11467295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66181464-A-G

11467323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66181435-A-G

11467536-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66181225-G-C

11467568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66181192-A-G

http://identifiers.org/hco/17/GRCh38#11467607-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66181153-A-C

http://identifiers.org/hco/17/GRCh38#11467685-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66181080-A-C

http://identifiers.org/hco/17/GRCh38#11467888-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66180889-A-C

11468084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66180692-G-A

11468174-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66180592-C-G

11468174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66180592-C-T

11468221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66180559-G-T

11468282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66180506-G-A

11468282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66180506-G-T

11468533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66180267-G-A

11468540-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66180260-T-A

11469117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66179710-T-C

11469148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66179678-G-A

11469218-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66179609-A-T

11469392-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66179447-C-G

11469560-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66179278-G-C

http://identifiers.org/hco/17/GRCh38#11469718-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66179134-A-C

http://identifiers.org/hco/17/GRCh38#11469861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66178993-C-A

11469874-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66178980-T-A

http://identifiers.org/hco/17/GRCh38#11469876-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66178978-A-C

11469970-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66178884-G-C

11470091-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66178798-C-G

11470109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66178781-T-C

11470115-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66178775-C-G

11470150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66178743-G-A

11470267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66178620-C-T

11470317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66178565-C-T

11470477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66178402-C-T

11470555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66178326-G-A

11470728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66178190-G-A

11470728-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66178190-G-C

http://identifiers.org/hco/17/GRCh38#11470758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66178169-C-A

11470774-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66178153-A-T

11470975-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66178008-T-G

11471159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66177988-A-G

11471159-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66177988-A-T

11472090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66177297-G-A

11472090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66177297-G-T

11472363-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66177147-A-T

11479977-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66169905-C-G

11480185-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66169707-T-G

11480464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66169423-C-T

11480470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66169417-G-A

11480914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66169033-G-A

http://identifiers.org/hco/17/GRCh38#11481849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66168274-C-A

11482192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66168003-A-G

11482192-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66168003-A-T

11482258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66167919-C-T

11482351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66167819-A-G

11482418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66167723-C-T

11482489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66167651-A-G

11482517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66167589-G-A

11482604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66167460-A-G

11482608-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66167456-T-A

11482834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66167204-G-A

11482834-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66167204-G-T

11482849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66167190-G-A

http://identifiers.org/hco/17/GRCh38#11482918-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66167126-A-C

11483291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66167050-A-G

11484043-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66166548-A-T

11484332-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66166229-G-C

11484787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66166104-A-G

11484991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66165896-C-T

11485026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66165872-G-A

11485671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66165167-G-A

11485889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66164946-T-C

11485890-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66164945-C-G

11485890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66164945-C-T

11486061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66164772-C-T

11486151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66164681-A-G

11486151-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66164681-A-T

11486264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66164613-T-C

11487481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66162419-C-T

11487534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66162375-A-G

11487588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66162306-G-A

11487734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66162163-G-T

11487738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66162159-A-G

11487801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66162096-G-A

11487997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66161950-T-C

11488176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66161850-A-G

11488432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66161611-T-C

http://identifiers.org/hco/17/GRCh38#11488493-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66161566-A-C

http://identifiers.org/hco/17/GRCh38#11488815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66161272-C-A

11489048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66161098-C-T

11489240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66160909-A-G

11489240-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66160909-A-T

http://identifiers.org/hco/17/GRCh38#11489364-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66160793-A-C

11489407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66160750-G-A

11489407-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66160750-G-C

11489625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66160522-A-G

11489720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66160445-G-A

11489785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66160376-G-A

11490018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66160201-A-G

11490126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66160113-G-A

11490490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66159775-T-C

11490603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66159683-G-A

11490609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66159677-G-A

11491183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66159308-A-G

11491191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66159300-G-A

11491200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66159291-C-T

11494062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66158105-T-C

11494076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66158092-G-A

11494095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66158074-C-T

11494264-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66157988-T-G

http://identifiers.org/hco/17/GRCh38#11494734-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66157433-A-C

11495014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66157185-C-T

11495170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66157022-C-T

11495436-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66156781-G-C

11495572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66156653-A-G

11495950-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66156313-A-T

11498986-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66156062-A-T

11499139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66155893-G-A

11499218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66155817-A-G

11499244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66155793-C-T

11499327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66155716-G-A

11499548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66155507-A-G

11500329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66155209-T-C

11500336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66155202-G-A

11500562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66154985-G-A

11501742-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66154186-C-G

11501775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66154145-G-A

http://identifiers.org/hco/17/GRCh38#11501790-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66154129-A-C

http://identifiers.org/hco/17/GRCh38#11501955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66153979-C-A

11502112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66153839-G-A

11502771-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66153804-T-G

11502893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66153701-G-A

11502893-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66153701-G-C

11503205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66153425-G-T

11503273-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66153356-G-C

11503288-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66153342-T-G

11503418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66153217-G-A

11503505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66153134-G-A

11504049-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66152601-A-T

11504178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66152475-G-A

11504538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66152126-A-G

11504700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66151974-G-T

11504738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66151940-G-A

11504799-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66151881-T-G

11505047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66151649-A-G

11505052-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66151644-T-A

11505060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66151633-G-A

11505123-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66151587-T-G

11505443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66151299-A-G

11505843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66151038-T-C

11505884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66150996-C-T

11505892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66150981-G-A

11506051-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66150660-C-G

11506075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66150636-A-G

11506144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66150519-T-C

11506152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66150511-C-T

11506384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66150293-A-G

11506522-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66150160-T-A

http://identifiers.org/hco/17/GRCh38#11506559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66150123-C-A

11506593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66150090-A-G

11506594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66150089-G-A

11506826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron_variant, undefined
orthologous variants: 66149881-G-T

11506867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron_variant, undefined
orthologous variants: 66149839-T-C

11510048-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66148522-G-C

11510083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66148500-A-G

11510121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66148462-G-A

11510209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66148395-G-T

11510861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66147890-A-G

11511603-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66147651-A-T

11513438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66147155-A-G

11513470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66147115-T-C

11513872-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66146658-G-C

11514151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66146381-A-G

http://identifiers.org/hco/17/GRCh38#11514157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66146375-C-A

11514224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66146305-T-C

11514570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66146229-G-T

11514599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66146200-T-C

11514934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66145877-T-C

11515125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66145638-A-G

11515396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66145577-C-T

11515416-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66145553-G-C

11515445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66145525-G-A

11515742-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66145277-A-T

11515888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66144954-C-T

11515934-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66144905-C-G

11515934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66144905-C-T

11516167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66144665-G-A

11516215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66144622-A-G

11516502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66144334-T-C

11516502-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66144334-T-G

11517056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66143968-T-C

11518634-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66142698-T-A

11518918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66141984-T-C

11518923-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66141979-C-G

11518923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66141979-C-T

11518998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66141909-C-T

11519012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66141895-G-A

11519751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66140863-C-T

11519867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66140751-G-A

11519868-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66140750-T-A

11520206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66140417-G-A

11520267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66140370-G-A

11520271-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66140366-A-T

11520936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66139739-A-G

11521439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66139260-T-C

http://identifiers.org/hco/17/GRCh38#11523121-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66138302-A-C

11523262-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66138159-T-G

11524167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66137648-A-G

11524309-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66137506-T-A

11524397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66137425-T-C

11524437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66137385-G-A

11524446-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66137376-T-A

11528168-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66132486-C-G

11528450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66132157-C-T

11528526-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66132090-A-T

11528719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66131855-C-T

11528803-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66131768-C-G

11529020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66131623-A-G

11529605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66131206-C-T

11529953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66130812-G-A

11529963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66130802-A-G

11530043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66130725-G-A

11530172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66130582-G-A

11530206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66130562-T-C

11530301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66130470-G-A

11530448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66130340-C-T

http://identifiers.org/hco/17/GRCh38#11530629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66130151-C-A

11530633-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66130147-C-G

11530633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66130147-C-T

11530681-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66130099-T-A

11530714-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66130066-G-C

11530980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66129814-A-G

11531095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66129703-A-G

11536133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66126744-T-C

11536359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66126629-T-C

11536441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66126545-A-G

11536856-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66126121-T-A

http://identifiers.org/hco/17/GRCh38#11536904-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66126073-A-C

http://identifiers.org/hco/17/GRCh38#11537095-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66125860-A-C

11539499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66124279-G-A

11540199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66123595-T-C

11541293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66122856-C-T

11541635-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66122604-T-A

11541892-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66122380-G-C

11547364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66120720-T-C

11547632-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66120452-G-T

11547976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66119872-C-T

11548096-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66119775-C-G

http://identifiers.org/hco/17/GRCh38#11548255-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66119624-A-C

11548320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66119498-C-T

11548552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66119264-C-T

11548947-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66118868-C-G

11549038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66118748-A-G

11549174-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66118569-T-G

11549191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66118552-T-C

11549209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66118495-C-T

11549530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66118168-T-C

11550454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66117082-G-T

11550654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66116891-C-T

11551277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66116330-G-A

11551646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66116123-T-C

11551652-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66116117-G-C

11551670-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66116099-T-G

11551674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66116095-G-A

11551841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66115868-G-A

11551979-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66115733-A-T

11552487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66115268-T-C

11552562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66115183-C-T

11552598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66115147-T-C

11552598-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66115147-T-G

11552616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66115129-G-A

11552795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66114705-G-A

http://identifiers.org/hco/17/GRCh38#11553078-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66114419-A-C

11553085-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66114412-A-T

11553455-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66114037-C-G

11553638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66113851-G-A

11553689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66113806-G-A

11553852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66113657-G-A

11554030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66113456-T-C

11554056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66113431-T-C

11554655-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66112831-C-G

11554730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66112757-G-A

11555497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66111085-G-A

11555497-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66111085-G-C

http://identifiers.org/hco/17/GRCh38#11555617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66110977-C-A

11555617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66110977-C-T

11555654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66110953-G-A

11555670-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66110937-T-A

11555670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66110937-T-C

11555670-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66110937-T-G

http://identifiers.org/hco/17/GRCh38#11555717-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66110887-A-C

11555748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: missense variant
orthologous variants: 66110855-C-T

11555856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: missense variant
orthologous variants: 66110747-A-G

11555874-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: missense variant
orthologous variants: 66110729-T-A

11555874-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: missense variant
orthologous variants: 66110729-T-G

11555966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66110636-C-T

http://identifiers.org/hco/17/GRCh38#11556031-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66110570-A-C

11556136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66110470-G-A

11556251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66110393-A-G

11556252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66110392-G-A

11556886-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66109698-C-G

11556886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66109698-C-T

11557035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66109616-T-C

11557123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66109531-T-C

11557695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66108897-T-C

http://identifiers.org/hco/17/GRCh38#11557745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66108852-C-A

11557745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: intron variant
orthologous variants: 66108852-C-T

11558240-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: missense variant
orthologous variants: 66108360-A-T

11558287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: missense variant
orthologous variants: 66108313-A-G

11558423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: 66108178-G-A

11558423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: 66108178-G-T

11558488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: 66108113-A-G

http://identifiers.org/hco/17/GRCh38#11558525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66108080-C-A

11558525-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: 66108080-C-G

11558525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: 66108080-C-T

11558658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: 66107957-G-A

11558658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: 66107957-G-T

http://identifiers.org/hco/17/GRCh38#11558811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66107796-C-A

http://identifiers.org/hco/17/GRCh38#11558896-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66107719-C-A

11559049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: 66107625-A-G

http://identifiers.org/hco/17/GRCh38#11559194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66107469-C-A

11559291-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: 66107371-G-C

11559291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: 66107371-G-T

11559321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: 66107341-G-A

11559321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: 66107341-G-T

11559420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: 66107241-A-G

11559421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: 66107240-G-A

11559421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: 66107240-G-T

http://identifiers.org/hco/17/GRCh38#11559426-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66107235-C-A

11559431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: 66107230-A-G

11559528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: 66107124-G-A

11559528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: 66107124-G-T

11559580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: 66107088-T-C

11559581-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: 66107087-T-A

11559652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: 66107004-G-A

11559652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: 66107004-G-T

11559690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: 66106978-T-C

11559790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: 66106883-C-T

11559980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: 66106700-A-G

11560089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: 66106597-T-C

http://identifiers.org/hco/17/GRCh38#11560090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66106596-C-A

11560144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: 66106541-G-T

11560286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: 66106409-C-T

11560308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: 66106387-T-C

11560703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: 66106022-G-T

11560733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: 66105952-G-T

http://identifiers.org/hco/17/GRCh38#11561297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66105174-C-A

http://identifiers.org/hco/17/GRCh38#11561544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66104970-C-A

11561559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: 66104955-T-C

11561613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: 66104906-T-C

11561904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: 66104650-G-T

11561935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: 66104615-G-A

11561935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: 66104615-G-T

11561955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: 66104595-G-T

http://identifiers.org/hco/17/GRCh38#11561997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66104555-C-A

11561997-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: 66104555-C-G

11562024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: 66104528-C-T

11562106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: 66104450-C-T

11562185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: 66104374-A-G

11562281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: 66104280-G-A

11562410-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: 66104150-G-C

11562410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: 66104150-G-T

http://identifiers.org/hco/17/GRCh38#11562544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66104022-C-A

11562553-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: 66104013-T-G

11562557-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: 66104009-T-A

11562557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: 66104009-T-C

11562675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: 66103877-T-C

11562675-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: 66103877-T-G

11562769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: 66103786-G-A

11562769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: 66103786-G-T

11562778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: 66103777-G-A

11562778-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: 66103777-G-C

11562778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: 66103777-G-T

http://identifiers.org/hco/17/GRCh38#11562877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66103699-C-A

11562887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: 66103689-G-A

11562887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: 66103689-G-T

11563122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: 66103476-G-A

http://identifiers.org/hco/17/GRCh38#11563325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#66103264-C-A

11563334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: 66103255-A-G

11563637-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: 66102964-T-A

11563934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: 66102693-T-C

11563978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34491
most severe consequence: 3 prime UTR variant
orthologous variants: 66102648-T-C