2426527-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155143230-C-G

2426545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155143212-C-T

2426646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155143133-G-A

2426832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155142987-C-T

2426919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155142916-G-A

2427059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155142776-C-T

2427140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155142693-G-A

2427150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155142684-G-A

2427257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155142585-G-T

2427302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155142531-G-T

2427380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155142444-C-T

2427381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155142443-G-A

2427428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155142405-C-T

2427489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155142326-G-A

2427799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155142067-G-A

2427962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155141982-G-A

2427962-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155141982-G-C

2428033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155141909-G-A

2428208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155141732-A-G

2428301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155141642-C-T

2428644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155141329-C-T

2428736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155141244-G-A

2428736-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155141244-G-T

2428836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155141151-C-T

2428837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155141150-C-T

2428969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155141072-G-A

2428983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155141058-A-G

2429054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155140989-G-A

2429054-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155140989-G-C

2429182-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155140866-C-G

2429259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155140826-G-T

2429535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155140572-G-A

2429872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155139651-G-A

2429872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155139651-G-T

2429873-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155139650-G-C

2429934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155139597-C-T

2429935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155139596-T-C

2429935-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155139596-T-G

2429950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155139586-A-G

http://identifiers.org/hco/1/GRCh38#2429953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155139583-C-A

2429953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155139583-C-T

2430080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155139459-A-G

2430238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, undefined
orthologous variants: 155139309-A-G

http://identifiers.org/hco/1/GRCh38#2430246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#155139301-C-A

2430249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155139297-G-A

2430249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155139297-G-T

2430294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155139260-A-G

2430395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 155139147-G-A

2430404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 155139138-A-G

http://identifiers.org/hco/1/GRCh38#2430505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155139058-C-A

2430505-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 155139058-C-G

2430505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 155139058-C-T

2430512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 155139052-T-C

http://identifiers.org/hco/1/GRCh38#2430551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155139015-C-A

2430551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: missense variant
orthologous variants: 155139015-C-T

2430577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: synonymous variant
orthologous variants: 155138989-G-A

2430577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: synonymous variant
orthologous variants: 155138989-G-T

2430614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: missense variant
orthologous variants: 155138952-A-G

2430864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155138752-C-T

2431073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155138582-C-T

2431438-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155138400-T-G

2431641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155138229-G-A

2431684-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155138190-C-G

2431748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155138140-T-C

2434091-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155134767-T-G

2434325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155134300-G-A

2436871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155133703-G-A

2437257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155133277-C-T

2437449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155133131-C-T

2437582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155132991-T-C

2437697-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155132883-C-G

2437703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155132877-G-T

2437754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155132839-T-C

2437757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155132836-G-A

2437777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155132810-C-T

2437933-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155132717-C-G

2437945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155132710-C-T

2438010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155132657-A-G

2438165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155132531-G-A

2438348-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155132408-T-G

2438352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155132404-C-T

2438518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155132289-G-A

2438682-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155132115-C-G

2438768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155131951-C-T

2438924-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155131810-T-G

2439820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155130934-G-A

2439920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155130832-G-T

2440013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155130757-G-A

2440013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155130757-G-T

2440243-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155130603-C-G

2440243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155130603-C-T

2440338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155130491-G-A

2440351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155130478-T-C

2441131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155130217-G-A

2441460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155129895-C-T

2441523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155129711-C-T

2441604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155129620-G-A

2441611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155129613-G-A

2441730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155129508-G-A

2441730-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155129508-G-C

2441980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155129265-A-G

2442001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155129241-T-C

2442584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155128711-G-A

2442754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155128554-G-A

2442943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155128383-G-A

http://identifiers.org/hco/1/GRCh38#2443056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155128283-C-A

2443056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155128283-C-T

2443317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155128021-G-A

2443317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155128021-G-T

2443351-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155127987-T-G

2443353-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155127985-T-A

2443353-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155127985-T-G

2443361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155127977-G-A

2443361-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155127977-G-C

2443361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155127977-G-T

2443540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155127850-G-T

2443575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155127815-G-A

2443575-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155127815-G-C

2443575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155127815-G-T

2443660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155127730-G-A

2443660-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155127730-G-C

2443963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155127430-C-T

2444231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155127150-C-T

2444267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155127114-C-T

2444453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155126936-C-T

2444481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155126908-C-T

2444782-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155126555-T-G

2444960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155126370-A-G

2445055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155126287-C-T

2445178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155126188-G-A

2445276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155126096-G-A

2445378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155126060-G-T

2445526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155125914-G-A

2445565-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155125869-C-G

2445565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155125869-C-T

2445590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155125841-C-T

2445684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155125721-A-G

2445691-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155125714-C-G

2445937-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155125471-C-G

2445953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155125454-C-T

2446899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155124472-G-A

http://identifiers.org/hco/1/GRCh38#2447082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155124246-C-A

2447082-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155124246-C-G

2447082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155124246-C-T

2447173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155124154-C-T

2447551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155123193-G-A

2447591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155123160-G-A

2447623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155123127-A-G

http://identifiers.org/hco/1/GRCh38#2447711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155123045-C-A

2447711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155123045-C-T

http://identifiers.org/hco/1/GRCh38#2447827-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155122908-A-C

2447895-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155122804-C-G

2447895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155122804-C-T

http://identifiers.org/hco/1/GRCh38#2447911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155122780-C-A

2447911-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155122780-C-G

2447911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155122780-C-T

2447932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155122759-G-A

2448235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155122491-C-T

2448244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155122479-C-T

2448261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155122468-C-T

2448385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155122347-T-C

2448387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155122345-G-T

2448391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155122341-C-T

2450110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155121099-G-A

2450401-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155120804-C-G

2450401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155120804-C-T

2450407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155120797-G-A

2450407-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155120797-G-C

2450524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155120683-G-A

2450524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155120683-G-T

http://identifiers.org/hco/1/GRCh38#2450547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155120666-C-A

2450697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155120473-C-T

2450774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155120367-G-T

http://identifiers.org/hco/1/GRCh38#2450833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155120293-C-A

2450833-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155120293-C-G

2451085-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155120018-G-C

2451238-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155119909-A-T

2451361-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155119829-G-C

2451435-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155119754-T-A

2451574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155119622-A-G

2451634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155119563-G-A

2451634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155119563-G-T

2451741-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155119489-G-T

2451886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, undefined
orthologous variants: 155119400-G-A

http://identifiers.org/hco/1/GRCh38#2452062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#155119189-C-A

2452062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, undefined
orthologous variants: 155119189-C-T

2452080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, undefined
orthologous variants: 155119163-C-T

2452323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155118899-C-T

http://identifiers.org/hco/1/GRCh38#2452624-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155118569-A-C

2452624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155118569-A-G

2452628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155118565-G-A

2452743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155118458-C-T

2452806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155118367-G-A

2452902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155118271-G-A

http://identifiers.org/hco/1/GRCh38#2453273-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155117965-C-A

2453666-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155117623-C-G

2453666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155117623-C-T

2453713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155117575-G-T

http://identifiers.org/hco/1/GRCh38#2453756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155117532-C-A

2453756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155117532-C-T

2453873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155117373-G-A

http://identifiers.org/hco/1/GRCh38#2455807-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155115119-C-A

2455822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155115113-C-T

2455953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155114984-G-A

2456194-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155114750-G-C

2456360-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155114464-A-T

2456540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155114279-C-T

2456583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155114222-G-A

2456813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155113998-T-C

2456884-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155113977-G-C

2456915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155113942-A-G

2456941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155113919-G-A

2456941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155113919-G-T

2457018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155113842-G-A

2457098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155113765-C-T

http://identifiers.org/hco/1/GRCh38#2457270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155113625-C-A

2457270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155113625-C-T

2457378-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155113516-C-G

2457380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155113514-C-T

2457389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155113505-C-T

2457859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155113136-T-C

2457871-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155113124-T-A

2457922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155113072-C-T

2458061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155112952-G-A

2458089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155112933-G-A

http://identifiers.org/hco/1/GRCh38#2460015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155109876-C-A

2460015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155109876-C-T

http://identifiers.org/hco/1/GRCh38#2460098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155109801-C-A

2460098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155109801-C-T

2460176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155109737-G-A

2460356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155109574-G-A

2460758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155109197-G-A

2460864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155109106-C-T

2461049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155108945-A-G

2461744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155108207-A-G

2462777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155107816-C-T

2462788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155107805-C-T

2462895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155107687-C-T

2462926-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155107656-C-G

2462926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155107656-C-T

2462951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155107635-C-T

2463381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155107273-C-T

2463584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155107070-G-A

2463584-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155107070-G-C

2463798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155106916-G-A

2463843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155106900-G-A

2463843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155106900-G-T

2463878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155106866-G-A

2463890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155106854-A-G

2464069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155106648-G-A

2464077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155106640-G-A

2464210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155106551-G-A

http://identifiers.org/hco/1/GRCh38#2465189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155105950-C-A

2465287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155105890-C-T

2465390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155105803-G-A

2465412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155105781-C-T

2465421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155105771-G-A

2465544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155105659-C-T

2465871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155105363-G-A

2465871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155105363-G-T

2466077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155105145-C-T

2466119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155105113-C-T

2466215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155105053-G-A

2466238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155105030-C-T

2466338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155104932-G-A

2466639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155104671-G-A

2466862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155104390-G-A

2466890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155104363-G-T

2466902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155104351-C-T

http://identifiers.org/hco/1/GRCh38#2466948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155104321-C-A

2466948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155104321-C-T

2467004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155104280-G-T

2467146-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155104185-G-C

2467213-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155104130-C-G

2467313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155104029-C-T

2467422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155103911-C-T

2467473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 155103859-G-A

2467473-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 155103859-G-C

2467473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 155103859-G-T

http://identifiers.org/hco/1/GRCh38#2467529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#155103790-C-A

2467533-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 155103786-G-C

2467533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 155103786-G-T

http://identifiers.org/hco/1/GRCh38#2467572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155103747-C-A

2467572-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 155103747-C-G

2467572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 155103747-C-T

2467680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155103635-A-G

2467680-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155103635-A-T

http://identifiers.org/hco/1/GRCh38#2467707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155103608-C-A

2467707-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155103608-C-G

2467707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155103608-C-T

2468181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, undefined
orthologous variants: 155103321-G-T

http://identifiers.org/hco/1/GRCh38#2468192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#155103310-C-A

2468560-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155103001-G-C

2468861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155102730-C-T

2468879-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155102710-G-C

2468941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155102653-C-T

http://identifiers.org/hco/1/GRCh38#2468969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155102612-C-A

2469178-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155102401-T-A

2469178-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155102401-T-G

2469360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155102215-G-A

2469410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155102162-C-T

2469588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155101981-G-A

2469588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155101981-G-T

2469589-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155101980-T-G

2469851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155101753-G-A

2469851-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155101753-G-C

2469866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155101738-G-A

2469910-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155101701-C-G

2469910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155101701-C-T

http://identifiers.org/hco/1/GRCh38#2470002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155101602-C-A

2470002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155101602-C-T

2470028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155101592-G-T

2470081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155101557-G-A

2470347-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155101236-C-G

2470926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155100742-C-T

2471109-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155100568-A-T

2471113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155100564-G-A

http://identifiers.org/hco/1/GRCh38#2471203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155100476-C-A

2472069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155099609-C-T

2472410-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155099293-A-T

2472920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155099108-G-A

2473106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155098920-C-T

2473225-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155098808-C-G

2473273-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155098772-C-G

2473297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155098749-C-T

2473340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155098718-G-A

2473557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155098560-T-C

2473588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155098530-C-T

2473723-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155098398-G-C

2473809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155098319-T-C

2473830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155098300-G-T

2473915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155098226-C-T

http://identifiers.org/hco/1/GRCh38#2474101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155097876-C-A

http://identifiers.org/hco/1/GRCh38#2474255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155097712-C-A

2474580-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155097386-G-C

2474846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155097036-G-A

2474883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155096991-C-T

http://identifiers.org/hco/1/GRCh38#2475024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#155096770-C-A

2475281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155096519-G-A

2475294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155096506-C-T

2475488-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155096350-G-C

2475488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155096350-G-T

2475691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155096178-C-T

2475736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155096132-G-A

2475826-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155096007-G-C

2475905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155095909-C-T

2475985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155095825-C-T

2475987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155095823-C-T

2475994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155095816-G-A

2476324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 155095465-T-C

2476324-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 155095465-T-G

2476351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 155095439-G-A

2476351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 155095439-G-T

2476359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 155095431-G-A

2476359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 155095431-G-T

2476380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 155095409-A-G

2476397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 155095392-G-A

2476397-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 155095392-G-T

2476416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 155095373-T-C

2476429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 155095360-G-A

2476429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 155095360-G-T

2476538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 155095257-G-A

2476578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 155095228-G-A

2476578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 155095228-G-T

http://identifiers.org/hco/1/GRCh38#2476610-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155095196-C-A

2476610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 155095196-C-T

2476673-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 155095133-A-T

2476739-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 155095067-G-C

2476739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 155095067-G-T

2476764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 155095041-G-A

2476764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 155095041-G-T

2476827-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 155094978-T-A

2476827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 155094978-T-C

2476837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 155094968-T-C

2476852-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 155094953-C-G

2476852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 155094953-C-T

2476866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 155094929-G-A

2476877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 155094918-G-A

2477024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 155094739-C-T

2477056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 155094711-G-A

2477141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 155094601-G-A

2477154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 155094588-G-A

http://identifiers.org/hco/1/GRCh38#2477258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155094477-C-A

2477402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 155094341-C-T

2477722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155094140-G-T

2477732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155094129-G-A

2477928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155093971-G-T

2478214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155093769-C-T

2478326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155093698-G-T

2478357-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155093669-G-T

2478639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155093428-G-A

2478645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155093422-G-A

2478645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155093422-G-T

2478655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155093410-G-T

2478656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155093409-A-G

http://identifiers.org/hco/1/GRCh38#2478660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155093405-C-A

2478660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155093405-C-T

2478693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155093375-G-A

2478693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155093375-G-T

2478702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155093366-T-C

2478713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155093351-G-A

2478713-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155093351-G-C

http://identifiers.org/hco/1/GRCh38#2478992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155093085-C-A

2478992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155093085-C-T

2478999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155093075-T-C

2478999-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155093075-T-G

http://identifiers.org/hco/1/GRCh38#2479008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155093069-C-A

2479008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155093069-C-T

http://identifiers.org/hco/1/GRCh38#2479057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155093028-C-A

2479057-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155093028-C-G

2479057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155093028-C-T

2479067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155093021-G-A

2479067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155093021-G-T

2479068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155093020-G-A

2479068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155093020-G-T

2479070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155093018-G-A

2479071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155093017-G-A

2479071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron variant
orthologous variants: 155093017-G-T

2479095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155093000-G-A

2479095-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155093000-G-C

2479107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155092988-G-A

2479107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155092988-G-T

2479118-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155092980-T-G

http://identifiers.org/hco/1/GRCh38#2479213-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155092889-A-C

2479213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155092889-A-G

2479278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155092826-G-A

2479278-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155092826-G-C

2479278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155092826-G-T

2479292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155092812-G-T

2479322-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155092777-T-A

2479322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155092777-T-C

2479329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155092770-G-A

2479329-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155092770-G-C

2479329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155092770-G-T

2479878-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155091472-G-C

2479984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 155091366-T-C

2480004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155091359-G-A

2480071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155091294-T-C

http://identifiers.org/hco/1/GRCh38#2480146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155091222-C-A

2480146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155091222-C-T

2480152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155091216-G-A

2480324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155091045-G-A

2480324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155091045-G-T

2480325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155091044-G-A

2480325-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155091044-G-C

2480346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155091027-G-A

2480346-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155091027-G-C

2480361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155091008-G-A

2480361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155091008-G-T

2480391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155090979-A-G

http://identifiers.org/hco/1/GRCh38#2480616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155090813-C-A

2480616-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155090813-C-G

http://identifiers.org/hco/1/GRCh38#2480617-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155090812-A-C

2480751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155090676-G-A

2480979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155090473-T-C

2481078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155090327-A-G

2481093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155090312-T-C

http://identifiers.org/hco/1/GRCh38#2481553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155089455-C-A

2481553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155089455-C-T

2481737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155089224-G-A

2481797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155089148-G-A

2481848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155089076-C-T

2484299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155087487-G-A

2484300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155087486-T-C

2484300-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155087486-T-G

2484332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155087457-G-A

2484332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155087457-G-T

2484360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155087437-G-T

2484426-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155087402-G-C

http://identifiers.org/hco/1/GRCh38#2484429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155087399-C-A

2484429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155087399-C-T

2485016-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155086936-C-G

2485016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155086936-C-T

2485111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155086851-G-A

2485111-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155086851-G-C

2485143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155086820-A-G

2486841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155085429-G-A

2486841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155085429-G-T

2486842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155085428-A-G

http://identifiers.org/hco/1/GRCh38#2486854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155085408-C-A

2486870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155085390-A-G

2486983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155085276-G-A

2487019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155085241-T-C

http://identifiers.org/hco/1/GRCh38#2487024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155085236-C-A

2487045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155085204-A-G

2487045-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155085204-A-T

2487161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155085113-G-A

2487161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155085113-G-T

http://identifiers.org/hco/1/GRCh38#2487196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155085083-C-A

2487196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155085083-C-T

http://identifiers.org/hco/1/GRCh38#2487390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155084879-C-A

2487390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155084879-C-T

http://identifiers.org/hco/1/GRCh38#2487399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155084856-C-A

2487399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155084856-C-T

2487407-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155084848-G-C

2487407-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155084848-G-T

2487408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155084847-G-A

2487408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155084847-G-T

2487441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155084815-G-A

http://identifiers.org/hco/1/GRCh38#2487442-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155084814-A-C

2487442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155084814-A-G

2487442-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155084814-A-T

http://identifiers.org/hco/1/GRCh38#2487450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155084809-C-A

http://identifiers.org/hco/1/GRCh38#2487460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155084799-C-A

2487593-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 155084645-T-A

2487699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155084539-T-C

2487708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155084530-A-G

2487765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155084463-A-G

2487767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155084461-G-A

2487767-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155084461-G-C

2487767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155084461-G-T

http://identifiers.org/hco/1/GRCh38#2487770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155084458-C-A

2487770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155084458-C-T

http://identifiers.org/hco/1/GRCh38#2487788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155084441-C-A

2487788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155084441-C-T

2487833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155084397-G-A

2487833-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155084397-G-C

2487833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155084397-G-T

2487980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155084217-T-C

2489146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155083538-G-A

2489146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155083538-G-T

2489149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155083535-G-A

2489149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155083535-G-T

2489167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155083517-G-A

2489205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 155083479-A-G

2489476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155083236-G-A

2489476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155083236-G-T

2489487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155083226-G-A

2489489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155083224-G-T

2489519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155083196-G-A

2489519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155083196-G-T

2489551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155083179-C-T

http://identifiers.org/hco/1/GRCh38#2489565-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155083165-A-C

http://identifiers.org/hco/1/GRCh38#2489616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155083138-C-A

2489616-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155083138-C-G

2489616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155083138-C-T

2489662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155083088-A-G

http://identifiers.org/hco/1/GRCh38#2489673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155083077-C-A

2489673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155083077-C-T

2489674-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155083076-T-A

2489676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155083074-G-A

2489676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155083074-G-T

http://identifiers.org/hco/1/GRCh38#2489682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155083069-C-A

2489682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155083069-C-T

2489793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155082982-G-A

2489793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155082982-G-T

2489841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155082934-G-A

2489841-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155082934-G-C

2489898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155082873-G-A

2489898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155082873-G-T

2490013-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155082054-T-A

2490013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155082054-T-C

2490024-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155082043-C-G

2490024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155082043-C-T

2490041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155082033-T-C

2490140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155081957-C-T

2490154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155081950-G-A

2490222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155081891-G-A

http://identifiers.org/hco/1/GRCh38#2490230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155081883-C-A

2490231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155081882-A-G

2490481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155081443-G-A

2490481-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155081443-G-C

2490481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155081443-G-T

2490542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155081366-G-A

2490543-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155081365-T-A

2490543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155081365-T-C

2490702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155081193-C-T

2490973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155080901-A-G

2491074-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155080843-A-T

2491093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155080820-G-A

2491093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155080820-G-T

2491117-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155080801-A-T

2491140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155080791-T-C

http://identifiers.org/hco/1/GRCh38#2491151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155080780-C-A

2491151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155080780-C-T

2491167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155080764-A-G

2491306-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155080631-C-G

2491315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155080622-T-C

2491340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155080597-A-G

2491372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155080565-G-A

http://identifiers.org/hco/1/GRCh38#2491386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155080549-C-A

2491403-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155080531-C-G

2491403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155080531-C-T

http://identifiers.org/hco/1/GRCh38#2491408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155080526-C-A

2491408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155080526-C-T

2491425-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155080512-T-A

http://identifiers.org/hco/1/GRCh38#2491431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155080506-C-A

2491432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155080505-A-G

2491962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155079964-T-C

2491962-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155079964-T-G

http://identifiers.org/hco/1/GRCh38#2492241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#155079707-C-A

2492241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 155079707-C-T

2492356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155079612-G-A

2492356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155079612-G-T

2492371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155079597-G-T

http://identifiers.org/hco/1/GRCh38#2492380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155079587-C-A

2492380-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155079587-C-G

2492401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155079566-G-A

2492401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155079566-G-T

2492428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155079474-G-T

http://identifiers.org/hco/1/GRCh38#2492432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155079470-C-A

2492432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155079470-C-T

http://identifiers.org/hco/1/GRCh38#2492443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155079459-C-A

2492443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155079459-C-T

2492472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155079427-G-A

2492509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155079402-G-A

2492509-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155079402-G-C

2492509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155079402-G-T

2492535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155079376-A-G

http://identifiers.org/hco/1/GRCh38#2492546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155079372-C-A

2492546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155079372-C-T

2492548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155079370-A-G

2493324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155079050-A-G

2493347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155079027-C-T

2493386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155078991-G-A

2493549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155078858-A-G

http://identifiers.org/hco/1/GRCh38#2493555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155078845-C-A

2493576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155078824-G-T

2493579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155078821-A-G

2493579-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155078821-A-T

2493657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155078767-G-A

2493657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155078767-G-T

2493680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155078745-C-T

http://identifiers.org/hco/1/GRCh38#2493812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155078658-C-A

2493812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155078658-C-T

2493813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155078657-A-G

2493833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155078637-G-A

2493833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155078637-G-T

http://identifiers.org/hco/1/GRCh38#2493834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155078635-C-A

2493834-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155078635-C-G

2493834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155078635-C-T

2493838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155078631-G-A

2493838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155078631-G-T

http://identifiers.org/hco/1/GRCh38#2493886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155078582-C-A

2493886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155078582-C-T

http://identifiers.org/hco/1/GRCh38#2493938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155078475-C-A

2493938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155078475-C-T

2493946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155078467-G-A

2493946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155078467-G-T

2493989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155078388-G-T

http://identifiers.org/hco/1/GRCh38#2494058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155078304-C-A

2494058-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155078304-C-G

2494058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155078304-C-T

http://identifiers.org/hco/1/GRCh38#2494243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155078068-C-A

2494243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155078068-C-T

http://identifiers.org/hco/1/GRCh38#2494313-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#155077999-C-A

2494313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 155077999-C-T

http://identifiers.org/hco/1/GRCh38#2494351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#155077940-C-A

2494351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 155077940-C-T

http://identifiers.org/hco/1/GRCh38#2494355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#155077936-C-A

2494355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 155077936-C-T

2494436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 155077807-G-T

http://identifiers.org/hco/1/GRCh38#2494437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#155077806-C-A

http://identifiers.org/hco/1/GRCh38#2494490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#155077754-C-A

2494490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 155077754-C-T

2494541-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 155077706-T-A

2494541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 155077706-T-C

2494541-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 155077706-T-G

2494542-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 155077705-T-A

2494542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 155077705-T-C

2494542-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 155077705-T-G

2494606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155077671-C-T

2494698-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155077626-G-C

http://identifiers.org/hco/1/GRCh38#2494710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155077614-C-A

2494710-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155077614-C-G

2494710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155077614-C-T

2494722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155077602-G-A

2494722-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155077602-G-C

2494722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155077602-G-T

2494730-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155077594-T-A

2494730-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155077594-T-G

http://identifiers.org/hco/1/GRCh38#2494760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155077565-C-A

2494796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155077528-G-A

2494796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155077528-G-T

http://identifiers.org/hco/1/GRCh38#2494878-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155077450-A-C

2494878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155077450-A-G

2494896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155077432-G-A

2494896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155077432-G-T

2494906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 155077422-A-G

2494907-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155077421-C-G

2494907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155077421-C-T

2494985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155077357-G-A

2494985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155077357-G-T

http://identifiers.org/hco/1/GRCh38#2495038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155077352-C-A

http://identifiers.org/hco/1/GRCh38#2495415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155077136-C-A

2495415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155077136-C-T

2495494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155077064-G-T

2495534-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155077024-A-T

2495541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 155077017-T-C

2495541-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 155077017-T-G

http://identifiers.org/hco/1/GRCh38#2495585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155076959-C-A

2495585-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155076959-C-G

2495860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155076710-G-A

2496053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155076530-G-A

2496063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155076520-G-A

2496063-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155076520-G-C

http://identifiers.org/hco/1/GRCh38#2496111-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155076474-A-C

2496210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 155076404-G-A

2496406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155076202-C-T

2496452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155076161-C-T

2496575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155075886-G-A

2496578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155075883-G-A

2496578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155075883-G-T

2496586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 155075862-G-A

http://identifiers.org/hco/1/GRCh38#2496587-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#155075856-A-C

2496587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 155075856-A-G

http://identifiers.org/hco/1/GRCh38#2496613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155075831-C-A

2496613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 155075831-C-T

2496662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155075782-A-G

2496662-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 155075782-A-T

2496763-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155075706-T-G

http://identifiers.org/hco/1/GRCh38#2496767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155075702-C-A

2496848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155075632-T-C

http://identifiers.org/hco/1/GRCh38#2496953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155075527-C-A

2496953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155075527-C-T

2497048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155075429-G-T

2497063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155075415-G-A

http://identifiers.org/hco/1/GRCh38#2497138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155075392-C-A

2497138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155075392-C-T

2497487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155075266-G-A

2497609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 155075144-G-A

2497609-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 155075144-G-C

2497609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 155075144-G-T

2497646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155075124-G-A

2497646-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155075124-G-C

2497647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155075123-G-A

2497647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155075123-G-T

2497652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155075118-G-A

2497689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155075100-G-A

2497689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155075100-G-T

2497781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155075015-G-A

2497781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155075015-G-T

2497786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155075010-G-A

2497786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155075010-G-T

2497877-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155074867-T-G

2497887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155074856-G-T

2497900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155074835-G-T

http://identifiers.org/hco/1/GRCh38#2497914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155074826-C-A

2497914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155074826-C-T

2498043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155074748-T-C

2498043-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155074748-T-G

2498093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155074742-G-A

2498093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155074742-G-T

2498106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155074729-G-A

2498106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155074729-G-T

http://identifiers.org/hco/1/GRCh38#2498122-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155074713-A-C

2498122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155074713-A-G

http://identifiers.org/hco/1/GRCh38#2498188-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155074669-A-C

2498188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155074669-A-G

2498188-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155074669-A-T

http://identifiers.org/hco/1/GRCh38#2498248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155074625-C-A

http://identifiers.org/hco/1/GRCh38#2498306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155074594-C-A

2498306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155074594-C-T

2498378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155074585-G-A

2498378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155074585-G-T

http://identifiers.org/hco/1/GRCh38#2498400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155074563-C-A

2498400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155074563-C-T

http://identifiers.org/hco/1/GRCh38#2498512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155074483-C-A

2498512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155074483-C-T

http://identifiers.org/hco/1/GRCh38#2498535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155074460-C-A

2498555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155074440-C-T

2498653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155074342-G-A

2498653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155074342-G-T

2498688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155074312-G-A

http://identifiers.org/hco/1/GRCh38#2498702-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155074300-A-C

2498702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155074300-A-G

2498765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155074248-G-A

2498987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155074068-G-A

2498987-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155074068-G-C

2499131-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155073974-C-G

2499191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155073914-A-G

2499644-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 155073649-A-T

2499664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155073629-G-A

2499664-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155073629-G-C

2499664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155073629-G-T

http://identifiers.org/hco/1/GRCh38#2499746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#155073542-C-A

2499874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155073440-G-A

2499874-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155073440-G-C

http://identifiers.org/hco/1/GRCh38#2499896-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155073419-C-A

2499899-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155073416-G-C

2499899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155073416-G-T

2499953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155073338-G-A

2499954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155073337-A-G

2499965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155073299-G-A

2499978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155073286-T-C

2500019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155073251-G-A

2500019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155073251-G-T

2500044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155073214-G-T

http://identifiers.org/hco/1/GRCh38#2500089-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155073166-C-A

2500156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155073081-G-A

2500156-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155073081-G-C

2500156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155073081-G-T

2500178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155073055-T-C

http://identifiers.org/hco/1/GRCh38#2500260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155072988-C-A

2500260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155072988-C-T

2500263-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155072985-G-C

2500263-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155072985-G-T

http://identifiers.org/hco/1/GRCh38#2500268-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155072980-C-A

2500268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155072980-C-T

http://identifiers.org/hco/1/GRCh38#2500366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155072886-C-A

http://identifiers.org/hco/1/GRCh38#2500423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155072826-C-A

2500423-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155072826-C-G

http://identifiers.org/hco/1/GRCh38#2500432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155072798-C-A

2500432-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155072798-C-G

2500432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155072798-C-T

http://identifiers.org/hco/1/GRCh38#2500883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155072372-C-A

2501052-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155072261-C-G

2501052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155072261-C-T

2501213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155072115-G-A

2501213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155072115-G-T

2501242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155072085-T-C

2501315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155072005-G-T

2501424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155071911-T-C

http://identifiers.org/hco/1/GRCh38#2501428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155071907-C-A

2501428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155071907-C-T

2501457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155071898-A-G

http://identifiers.org/hco/1/GRCh38#2501484-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155071865-A-C

2501484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155071865-A-G

2501536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155071815-A-G

2501667-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155071721-G-C

2501667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155071721-G-T

2501672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155071716-G-A

2501672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155071716-G-T

2501692-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155071704-T-G

http://identifiers.org/hco/1/GRCh38#2501787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155071666-C-A

2501787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155071666-C-T

2501865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155071632-G-A

2501865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155071632-G-T

http://identifiers.org/hco/1/GRCh38#2501883-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155071617-A-C

2501883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155071617-A-G

2501883-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155071617-A-T

http://identifiers.org/hco/1/GRCh38#2501889-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155071611-A-C

2501889-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155071611-A-T

2501950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155071573-G-A

2501950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155071573-G-T

http://identifiers.org/hco/1/GRCh38#2501994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155071544-C-A

2502073-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155071510-G-C

2502073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155071510-G-T

2502339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 155071244-G-A

2502339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 155071244-G-T

2502349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155071234-G-A

2502349-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155071234-G-C

2502349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155071234-G-T

2502370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155071213-G-A

2502370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155071213-G-T

2502529-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155071048-T-A

2502529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155071048-T-C

2502555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 155071022-G-A

2502555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 155071022-G-T

2502594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155070983-G-T

2502642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 155070935-G-T

2502643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155070934-G-A

2502643-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155070934-G-C

2503021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155070599-G-A

2503021-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155070599-G-C

2503021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155070599-G-T

2503132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155070507-G-A

2503132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155070507-G-T

2503173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155070467-T-C

2503222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155070419-C-T

2503249-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155070396-C-G

http://identifiers.org/hco/1/GRCh38#2503313-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155070318-C-A

2503313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155070318-C-T

2503364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155070257-C-T

http://identifiers.org/hco/1/GRCh38#2503374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155070247-C-A

2503374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155070247-C-T

2503431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155070204-G-A

2503431-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155070204-G-C

2503431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155070204-G-T

2503441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155070194-G-A

2503441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155070194-G-T

http://identifiers.org/hco/1/GRCh38#2503575-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155069890-A-C

2503575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155069890-A-G

2503575-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155069890-A-T

2503691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155069767-G-A

2503691-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155069767-G-C

2503691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155069767-G-T

http://identifiers.org/hco/1/GRCh38#2503718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155069718-C-A

2503753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155069683-T-C

2503822-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155069588-A-T

2503856-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155069536-C-G

2503856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155069536-C-T

http://identifiers.org/hco/1/GRCh38#2503858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155069534-C-A

2503858-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155069534-C-G

2503858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155069534-C-T

2503871-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155069521-T-A

2503871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155069521-T-C

http://identifiers.org/hco/1/GRCh38#2504009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155069333-C-A

2504009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155069333-C-T

2504085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 155069257-G-A

2504085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 155069257-G-T

http://identifiers.org/hco/1/GRCh38#2504188-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155069112-A-C

2504230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155069070-G-A

2504230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155069070-G-T

2504260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155069040-G-T

2504368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155068962-C-T

2504374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155068956-G-A

2504710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155068620-G-A

2504710-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155068620-G-C

2504803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155068527-G-A

2504803-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155068527-G-C

2504803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155068527-G-T

http://identifiers.org/hco/1/GRCh38#2504995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155068335-C-A

2504995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155068335-C-T

http://identifiers.org/hco/1/GRCh38#2505001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155068329-C-A

2505001-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155068329-C-G

2505001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155068329-C-T

http://identifiers.org/hco/1/GRCh38#2505057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155068273-C-A

2505057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 155068273-C-T

2505072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 155068258-A-G

2505072-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 155068258-A-T

2505188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155068142-A-G

http://identifiers.org/hco/1/GRCh38#2505255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155068071-C-A

2505255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29037
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 155068071-C-T