http://identifiers.org/hco/6/GRCh38#116529039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33964849-C-A

116529126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 33964762-G-T

116529145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 33964743-T-C

116529184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 33964700-G-A

116529186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 33964698-G-T

116529206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33964678-G-A

116529206-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33964678-G-C

http://identifiers.org/hco/6/GRCh38#116529297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33964602-C-A

116529297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33964602-C-T

116529317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33964582-A-G

116529523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33964453-A-G

116529535-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33964446-T-A

116529538-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33964443-G-C

116529974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33963521-G-A

116530136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33963395-A-G

116530468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33962991-G-A

116530484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33962975-T-C

116530544-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33962920-A-T

http://identifiers.org/hco/6/GRCh38#116530681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33962777-C-A

116530947-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33962582-T-A

116530947-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33962582-T-G

http://identifiers.org/hco/6/GRCh38#116530949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33962580-C-A

116530949-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33962580-C-G

116530949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33962580-C-T

116530987-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33962553-T-A

116531112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33962431-G-A

116531112-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33962431-G-C

116531265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33962283-A-G

116531476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33961864-G-A

116531554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33961805-G-A

116531641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33961728-T-C

116531745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33961623-C-T

116531815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33961553-T-C

116532004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33961459-G-A

http://identifiers.org/hco/6/GRCh38#116532012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33961451-C-A

116532012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33961451-C-T

116532034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33961429-T-C

116532847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33959913-A-G

116533006-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33959767-G-C

116533071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33959711-G-A

116533084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33959697-T-C

http://identifiers.org/hco/6/GRCh38#116533089-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33959692-C-A

http://identifiers.org/hco/6/GRCh38#116533334-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33959476-A-C

116533605-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron_variant, undefined
orthologous variants: 33959220-T-G

116533613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33959212-G-A

116533667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron_variant, undefined
orthologous variants: 33959164-A-G

116533846-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33959023-C-G

116534107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33958376-C-T

116534108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33958375-G-T

116534120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33958368-C-T

116534188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33958302-T-C

116534210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33958280-T-C

http://identifiers.org/hco/6/GRCh38#116534262-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33958217-A-C

116534407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33957976-G-A

116534413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33957970-T-C

http://identifiers.org/hco/6/GRCh38#116534467-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33957917-A-C

116534467-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33957917-A-T

116534626-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33957756-G-C

116534633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33957542-T-C

116534738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33957431-A-G

116534779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33957390-A-G

116534870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33957304-G-A

http://identifiers.org/hco/6/GRCh38#116535133-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33951667-A-C

116535443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33951166-C-T

http://identifiers.org/hco/6/GRCh38#116535561-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33951051-A-C

116535670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33950934-T-C

116535683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33950921-T-C

116535774-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33950113-T-A

116535877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33949965-A-G

http://identifiers.org/hco/6/GRCh38#116535916-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33949929-A-C

116535948-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33949903-A-T

116536437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 33947754-T-C

116536588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33947608-T-C

116536667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33947552-G-A

116536669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33947550-G-A

116536765-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33947458-A-T

116536930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33947299-C-T

116537039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33947189-A-G

116537115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33947116-G-A

116537182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33947059-G-A

116538347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33944772-A-G

116538503-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33944641-C-G

116538697-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33944430-T-G

116539264-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33943753-T-A

116539455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33943528-T-C

116539799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33943179-A-G

116540284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33941470-A-G

116540284-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33941470-A-T

116540285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33941469-T-C

116540367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron_variant, missense_variant
orthologous variants: 33941234-G-A

116540451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron_variant, missense_variant
orthologous variants: 33941150-A-G

116540451-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron_variant, missense_variant
orthologous variants: 33941150-A-T

116540497-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33941111-C-G

116540597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33941070-G-T

116540637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33941030-A-G

http://identifiers.org/hco/6/GRCh38#116540653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33941014-C-A

116540679-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33940990-T-G

116540907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33940806-G-A

116541604-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33939795-A-T

116541880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33939561-A-G

116541932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33939510-T-C

http://identifiers.org/hco/6/GRCh38#116542050-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33939395-A-C

116542078-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33939367-T-A

116542121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33939320-G-T

116542166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33939279-G-A

116542192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33939253-G-A

116542215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33939230-A-G

http://identifiers.org/hco/6/GRCh38#116542332-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33939127-A-C

116542332-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33939127-A-T

116542539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33938913-C-T

116542755-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33936638-A-T

116542808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33936587-A-G

116543091-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33936292-C-G

116543268-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 33936136-C-G

116543268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 33936136-C-T

116543273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 33936131-A-G

116543274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 33936130-T-C

116543353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 33936053-C-T

116543489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33935919-A-G

http://identifiers.org/hco/6/GRCh38#116543522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33935886-C-A

116543522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33935886-C-T

116543621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33935812-A-G

116543633-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33935800-T-G

116543689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33935740-A-G

116543689-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33935740-A-T

116543716-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33935715-C-G

http://identifiers.org/hco/6/GRCh38#116543754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33935675-C-A

116543754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33935675-C-T

116543869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 33935565-A-G

116544076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33934311-C-T

116544432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33933928-T-C

116544674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33933671-A-G

116544718-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33933627-C-G

http://identifiers.org/hco/6/GRCh38#116544741-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33933604-C-A

116544788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33933555-C-T

http://identifiers.org/hco/6/GRCh38#116544997-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33933334-A-C

116545059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33933252-A-G

116545280-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33933082-A-T

116545330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33933028-G-A

116545330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33933028-G-T

116545336-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33933022-T-A

116545336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33933022-T-C

http://identifiers.org/hco/6/GRCh38#116545370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33933000-C-A

116545383-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33932983-T-A

116545421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33932944-A-G

116545598-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 33932770-T-A

116545638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 33932730-G-A

116545638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 33932730-G-T

116546253-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33932148-C-G

116546610-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33931804-G-C

116546838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33931577-T-C

116547140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33931293-C-T

116547562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33929217-G-T

116547610-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33929171-T-A

116547610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33929171-T-C

116547610-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33929171-T-G

116547707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33929075-G-A

116549328-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33924919-C-G

116549328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33924919-C-T

116549387-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33924872-C-G

116549673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33924035-G-A

116550252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33923789-T-C

116550281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33923760-A-G

116550281-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33923760-A-T

116550567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33923532-T-C

116550896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33923182-C-T

http://identifiers.org/hco/6/GRCh38#116550914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#33923163-C-A

116551087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33922993-C-T

116551196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33922848-G-T

116551299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33922792-C-T

116551937-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33921708-T-A

116552218-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33921334-T-G

116552383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33921227-C-T

116553208-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33920806-T-G

116553281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33920758-T-C

http://identifiers.org/hco/6/GRCh38#116553341-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33920711-C-A

116553341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33920711-C-T

116553377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33920675-A-G

116553629-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33920425-T-G

116553652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33920405-G-A

116553652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33920405-G-T

116553683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33920372-G-T

http://identifiers.org/hco/6/GRCh38#116553694-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33920361-A-C

116553694-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33920361-A-T

116553878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron_variant, missense_variant
orthologous variants: 33920179-G-A

116553878-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron_variant, missense_variant
orthologous variants: 33920179-G-C

116554146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron_variant, missense_variant
orthologous variants: 33919908-G-T

http://identifiers.org/hco/6/GRCh38#116554274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33919780-C-A

116554382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33919655-A-G

116554399-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33919629-T-A

116554400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33919628-A-G

http://identifiers.org/hco/6/GRCh38#116554425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33919594-C-A

116554429-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33919590-C-G

http://identifiers.org/hco/6/GRCh38#116554464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33919556-C-A

116554464-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33919556-C-G

http://identifiers.org/hco/6/GRCh38#116554471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33919549-C-A

116554471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33919549-C-T

116554611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33919360-C-T

116554615-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33919356-C-G

116554839-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33919128-C-G

116555044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33918954-T-C

116557336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33918368-T-C

116557541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33918153-G-A

116557668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33918027-A-G

116557693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: intron variant
orthologous variants: 33918008-A-G

116557999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: missense_variant, undefined
orthologous variants: 33917712-A-G

116558216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 33917495-A-G

116558221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 33917490-C-T

116558292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 33917430-T-C

http://identifiers.org/hco/6/GRCh38#116558354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33917371-C-A

116558354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: 3 prime UTR variant
orthologous variants: 33917371-C-T

116558478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: 3 prime UTR variant
orthologous variants: 33917225-A-G

116558479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: 3 prime UTR variant
orthologous variants: 33917224-G-A

http://identifiers.org/hco/6/GRCh38#116558562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33917144-C-A

116558562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: 3 prime UTR variant
orthologous variants: 33917144-C-T

116558850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: 3 prime UTR variant
orthologous variants: 33916906-G-T

116559283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: 3 prime UTR variant
orthologous variants: 33916286-T-C

http://identifiers.org/hco/6/GRCh38#116559417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33916170-C-A

116559504-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: 3 prime UTR variant
orthologous variants: 33916084-T-A

116560417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: 3 prime UTR variant
orthologous variants: 33914987-C-T

116560430-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: 3 prime UTR variant
orthologous variants: 33914974-T-G

116560673-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: 3 prime UTR variant
orthologous variants: 33914774-T-G

116560689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: 3 prime UTR variant
orthologous variants: 33914759-T-C

116560858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: 3 prime UTR variant
orthologous variants: 33913631-T-C

116561113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21094
most severe consequence: 3 prime UTR variant
orthologous variants: 33913389-A-G