74748889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: synonymous variant
orthologous variants: 99629631-T-C

http://identifiers.org/hco/11/GRCh38#74748896-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99629624-C-A

74748896-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: missense variant
orthologous variants: 99629624-C-G

74748896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: missense variant
orthologous variants: 99629624-C-T

74748965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: missense variant
orthologous variants: 99629555-G-A

74749066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: synonymous variant
orthologous variants: 99629475-G-A

74749066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: synonymous variant
orthologous variants: 99629475-G-T

http://identifiers.org/hco/11/GRCh38#74749137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: stop gained
orthologous variants: http://identifiers.org/mco/7/GRCm39#99629404-C-A

74749137-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: missense variant
orthologous variants: 99629404-C-G

74749137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: missense variant
orthologous variants: 99629404-C-T

http://identifiers.org/hco/11/GRCh38#74749283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99629267-C-A

74749283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: missense variant
orthologous variants: 99629267-C-T

74749295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: missense variant
orthologous variants: 99629255-G-A

74749295-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: missense variant
orthologous variants: 99629255-G-C

74749295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: stop gained
orthologous variants: 99629255-G-T

74749297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: synonymous variant
orthologous variants: 99629253-G-A

74749297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: missense variant
orthologous variants: 99629253-G-T

74749302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: missense variant
orthologous variants: 99629248-G-A

74749302-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: missense variant
orthologous variants: 99629248-G-C

74749302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: missense variant
orthologous variants: 99629248-G-T

74749388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, missense_variant
orthologous variants: 99629171-G-A

74749388-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, missense_variant
orthologous variants: 99629171-G-C

74749388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, missense_variant
orthologous variants: 99629171-G-T

http://identifiers.org/hco/11/GRCh38#74749396-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99629163-A-C

74749396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 99629163-A-G

74749396-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 99629163-A-T

74749413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, stop_gained
orthologous variants: 99629148-G-A

74749413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, missense_variant
orthologous variants: 99629148-G-T

http://identifiers.org/hco/11/GRCh38#74749476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99629086-C-A

74749476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99629086-C-T

http://identifiers.org/hco/11/GRCh38#74749511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99629052-C-A

74749511-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99629052-C-G

74749750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99628812-T-C

74749874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99628718-G-A

74749914-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99628670-G-C

74750117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99628452-G-A

74750433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99628168-T-C

74750564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99628050-T-C

74750593-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99628007-T-A

http://identifiers.org/hco/11/GRCh38#74751293-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99627924-A-C

74751293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99627924-A-G

74751293-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99627924-A-T

74751384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99627891-C-T

74751653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99627634-C-T

74753479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99625452-G-A

74754318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99624498-A-G

74754863-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99624291-T-G

74754982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99624153-T-C

74755009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99624126-T-C

74755065-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99624073-G-C

74755166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99623984-G-A

http://identifiers.org/hco/11/GRCh38#74755170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99623980-C-A

74755171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99623979-C-T

74755386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99623750-C-T

74770233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99621513-G-A

74770465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99620993-C-T

74770562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99620899-A-G

74772493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99620674-T-C

74772507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99620665-G-T

74772508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99620664-A-G

74772508-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99620664-A-T

74772703-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99620491-G-C

74772798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99620167-A-G

74772821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99620144-T-C

74772944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99620032-A-G

74773156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99619776-T-C

74773183-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99619763-C-G

74773317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99619649-A-G

74773436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99619535-A-G

74773478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99619493-A-G

74773505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99619468-C-T

74773744-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99619256-T-G

74773844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99619165-T-C

74774601-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99617658-T-G

74776680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99616837-A-G

74776689-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99616828-T-G

74776972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99616577-A-G

74776980-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99616569-T-G

74777428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99615834-G-A

74777560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99615711-G-T

74777572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99615699-G-A

74780523-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99615258-G-C

74781001-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99614790-T-A

74781190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99614603-T-C

74781305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99614491-G-T

74782914-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99613400-T-G

74782927-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99613358-A-T

74782942-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99613343-A-T

74782954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99613331-G-T

74783060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99613124-C-T

74783205-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99612850-A-T

74783420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99612584-T-C

74783647-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99612318-C-G

74783647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99612318-C-T

74783660-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99612305-G-C

74783660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99612305-G-T

http://identifiers.org/hco/11/GRCh38#74784285-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99611400-A-C

74784317-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99611291-A-T

74784659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99610932-C-T

74785382-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99608208-T-G

74786657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99607626-T-C

74787591-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99606723-T-G

74787683-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99606642-C-G

74787694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99606631-C-T

74788001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99606353-C-T

74789108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99606142-A-G

74789115-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99606135-G-C

74789617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99604754-T-C

74789661-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 99604710-C-G

74789661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 99604710-C-T

http://identifiers.org/hco/11/GRCh38#74789670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99604701-C-A

74789671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 99604700-T-C

74789679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 99604692-G-A

74789702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99604669-A-G

74789715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99604653-G-A

74789715-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99604653-G-C

74789793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99604577-A-G

74793935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99603688-T-C

http://identifiers.org/hco/11/GRCh38#74794001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99603639-C-A

74794024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99603624-G-A

74794075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99603556-C-T

74794081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99603550-A-G

74794102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99603529-T-C

74794359-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99603289-T-G

74797403-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99602539-A-T

74797564-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99602434-C-G

74797571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99602427-C-T

74797667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99602342-T-C

74799358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99602171-T-C

74799358-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99602171-T-G

74799497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99602090-A-G

74800558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99598507-G-A

74800621-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron variant
orthologous variants: 99598445-T-G

74808681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99595882-A-G

74808875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99595731-T-C

74808894-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99595713-C-G

74808894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99595713-C-T

74808959-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99595670-T-G

74809154-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99595495-C-G

74809340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99593186-T-C

74809487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99593042-G-A

74809809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99592879-T-C

http://identifiers.org/hco/11/GRCh38#74809816-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99592872-A-C

74809816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99592872-A-G

74809855-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99592838-C-G

74810048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99592429-G-A

74810048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99592429-G-T

74810086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99592393-C-T

74810154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99592343-C-T

74810331-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, splice_donor_variant, undefined
orthologous variants: 99591785-G-C

http://identifiers.org/hco/11/GRCh38#74810428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99591724-C-A

http://identifiers.org/hco/11/GRCh38#74810439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99591713-C-A

http://identifiers.org/hco/11/GRCh38#74810440-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99591712-A-C

74810468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99591684-G-A

74810468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99591684-G-T

http://identifiers.org/hco/11/GRCh38#74810471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99591681-C-A

74810471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99591681-C-T

http://identifiers.org/hco/11/GRCh38#74810479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99591672-C-A

74810479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99591672-C-T

74810482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99591669-G-T

74810509-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99591644-A-T

74810742-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99591410-T-A

74810896-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99591129-T-A

74810896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99591129-T-C

http://identifiers.org/hco/11/GRCh38#74811110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99590937-C-A

74811698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99590217-C-T

74811838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99590078-C-T

74811843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99590073-A-G

74812073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99586830-C-T

74812242-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99586659-T-G

74812292-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99586600-T-G

74812777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99586106-G-T

http://identifiers.org/hco/11/GRCh38#74812917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99585965-C-A

http://identifiers.org/hco/11/GRCh38#74813023-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99585893-A-C

74813163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99585766-G-T

74813252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99585699-T-C

74813611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99585364-T-C

74817698-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 99584383-T-A

74817743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99584340-G-A

74817743-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99584340-G-C

74817743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99584340-G-T

74817745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99584338-G-A

74817814-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99584306-G-C

74818283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99583940-A-G

74818479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99583782-A-G

74818700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99583635-A-G

74831347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99578824-A-G

74831363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99578808-A-G

http://identifiers.org/hco/11/GRCh38#74831364-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99578807-A-C

74831364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99578807-A-G

74831392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99578774-A-G

74831435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99578733-G-A

74831435-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99578733-G-C

74831660-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99578517-T-A

74831690-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99578487-T-A

74831767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99578456-A-G

http://identifiers.org/hco/11/GRCh38#74831784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99578439-C-A

74831828-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99578395-G-T

74831849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99578375-T-C

http://identifiers.org/hco/11/GRCh38#74831886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99578338-C-A

74831935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99578291-G-A

74831935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99578291-G-T

74832025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99578259-G-A

74832141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99578169-T-C

http://identifiers.org/hco/11/GRCh38#74832248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99578081-C-A

74832316-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99578019-C-G

74832316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99578019-C-T

http://identifiers.org/hco/11/GRCh38#74832470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99577876-C-A

74832470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99577876-C-T

74832533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99577815-A-G

74832635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99577734-A-G

74832706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99577674-G-A

74832892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99577540-T-C

74832955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99577482-G-T

74833374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99577136-A-G

http://identifiers.org/hco/11/GRCh38#74833911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99576995-C-A

74833960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99576951-A-G

74834564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99576497-G-T

74834579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99576480-G-A

74834579-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99576480-G-C

74834579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99576480-G-T

74834581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99576478-G-A

74834581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99576478-G-T

http://identifiers.org/hco/11/GRCh38#74834779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99576294-C-A

74834779-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99576294-C-G

74834779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99576294-C-T

74834810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99576266-G-A

74834856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99576221-T-C

74834864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99576213-A-G

http://identifiers.org/hco/11/GRCh38#74834869-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99576208-A-C

74834907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99576171-A-G

http://identifiers.org/hco/11/GRCh38#74835438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99575815-C-A

74835438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99575815-C-T

http://identifiers.org/hco/11/GRCh38#74835469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99575782-C-A

http://identifiers.org/hco/11/GRCh38#74835475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99575776-C-A

74835521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, undefined
orthologous variants: 99575713-G-A

74835696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 99575538-C-T

74835834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 99575400-C-T

74835906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 99575328-G-A

74836211-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 99575023-G-C

74836212-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 99575022-G-C

74836213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 99575021-G-A

74836269-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 99574965-G-C

74836386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 99574848-A-G

http://identifiers.org/hco/11/GRCh38#74836391-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99574843-A-C

http://identifiers.org/hco/11/GRCh38#74836443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99574791-C-A

74836644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 99574593-G-A

74836644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 99574593-G-T

74836946-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99574276-G-C

74836946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99574276-G-T

74836995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99574226-G-A

74837062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99574148-T-C

74837062-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99574148-T-G

74837129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99574087-T-C

http://identifiers.org/hco/11/GRCh38#74837222-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99573989-A-C

74837222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99573989-A-G

74837344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99573886-A-G

74837473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99573774-C-T

74837609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99573636-A-G

http://identifiers.org/hco/11/GRCh38#74837620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99573626-C-A

74837645-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99573602-G-C

74838045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99573247-G-T

74838066-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99573226-C-G

http://identifiers.org/hco/11/GRCh38#74838734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99572794-C-A

74838734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99572794-C-T

74838772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99572756-T-C

74838772-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99572756-T-G

74838790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99572742-G-T

http://identifiers.org/hco/11/GRCh38#74839165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99572380-C-A

74839173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99572372-T-C

http://identifiers.org/hco/11/GRCh38#74839183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99572362-C-A

http://identifiers.org/hco/11/GRCh38#74839346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99572204-C-A

74839348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99572202-T-C

74839422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99572138-G-T

74839468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99572096-A-G

74839518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99572051-T-C

http://identifiers.org/hco/11/GRCh38#74839527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99572044-C-A

74839527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99572044-C-T

74839546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99572025-T-C

74839656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99571937-G-A

74839656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99571937-G-T

74839662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99571928-G-T

74839664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99571926-G-T

74839682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99571908-A-G

74839788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99571835-G-A

74839788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99571835-G-T

74840001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99571581-T-C

74840009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99571570-G-T

74840454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99571198-T-C

74840696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99571000-A-G

http://identifiers.org/hco/11/GRCh38#74840698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99570998-C-A

74840698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99570998-C-T

74840717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99570984-A-G

74840738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99570965-G-A

74841186-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99570655-T-G

74841310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99570564-G-A

74841310-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99570564-G-T

http://identifiers.org/hco/11/GRCh38#74841476-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99570369-A-C

http://identifiers.org/hco/11/GRCh38#74841577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99570288-C-A

http://identifiers.org/hco/11/GRCh38#74841799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99570073-C-A

74841863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99570012-G-A

74841998-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99569906-A-T

74842272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99569600-G-A

74842272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26961
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99569600-G-T