2337583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 74787822-G-A

2337583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 74787822-G-T

2337635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 74787770-G-A

http://identifiers.org/hco/17/GRCh38#2337682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74787712-C-A

2337682-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 74787712-C-G

2337682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 74787712-C-T

2337751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74787643-G-A

2337751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74787643-G-T

2337757-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74787637-T-A

2337757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74787637-T-C

http://identifiers.org/hco/17/GRCh38#2337795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74787600-C-A

2337795-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74787600-C-G

2337795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74787600-C-T

2337801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74787594-G-A

2337801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74787594-G-T

http://identifiers.org/hco/17/GRCh38#2337809-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74787586-A-C

2337809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74787586-A-G

2337809-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74787586-A-T

2337817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 74787580-G-A

2337817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 74787580-G-T

2337869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74787530-T-C

2337869-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74787530-T-G

2337879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74787520-G-A

2337879-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74787520-G-T

2337885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74787514-C-T

2337999-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74787405-G-C

2338018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74787386-G-A

2338259-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74787180-C-G

2338316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74787121-T-C

2338608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74786827-C-T

2338618-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74786817-G-C

2338716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74786740-A-G

2340512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 74786263-C-T

2341707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 74785318-C-T

2342291-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74784509-G-C

2342291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74784509-G-T

2342295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74784505-A-G

2342315-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74784486-T-G

2342354-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74784456-T-A

2342354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74784456-T-C

2342354-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74784456-T-G

2342433-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74784372-C-G

2343129-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74783455-C-G

2343512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74783012-A-G

2343512-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74783012-A-T

2343655-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 74782706-T-A

2343673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74782667-G-A

2343679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74782639-G-A

2343684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74782634-A-G

2343689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74782547-A-G

2343786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 74782454-A-G

2343786-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 74782454-A-T

2344017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74774573-G-A

2344017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74774573-G-T

2344500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74774104-C-T

2344665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74773950-A-G

2344709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74773908-A-G

2344878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74773392-G-A

2344949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74773332-T-C

2344965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74773321-T-C

2345165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74773129-G-A

2347631-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74768581-G-C

2347879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74767984-C-T

2347892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74767972-C-T

2347946-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74767947-C-G

2348038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74767874-T-C

2348183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74767725-A-G

2348185-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74767723-C-G

2348198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74767710-C-T

2348641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74767330-C-T

2350980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74766793-T-C

2351233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74766553-A-G

2351507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74766281-T-C

2351526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74766260-G-A

2351960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74766015-G-A

2352012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74765962-T-C

2352103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74765858-T-C

http://identifiers.org/hco/17/GRCh38#2352149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74765813-C-A

2352455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74765578-T-C

2352500-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74765542-A-T

2352667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74765380-T-C

2352746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74765311-T-C

2352746-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74765311-T-G

http://identifiers.org/hco/17/GRCh38#2353371-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74765059-A-C

2357055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74763994-T-C

2357117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74763931-G-A

2357343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74763745-A-G

2357581-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74763570-T-A

2357717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74763530-C-T

2357719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74763528-A-G

2357803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74763439-G-A

2358054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74763200-A-G

2358195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74763089-G-A

2359208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74762490-C-T

2359277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74762429-A-G

2359535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74762216-G-T

2359776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 74761988-C-T

2359797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 74761967-G-A

2359904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74761860-G-A

2359983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74761787-C-T

2360386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74761238-C-T

2360576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74761064-G-A

http://identifiers.org/hco/17/GRCh38#2360912-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74760906-A-C

2360918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74760899-T-C

2361226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74760615-G-A

2361274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74760568-C-T

2361532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74760297-G-A

2361532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74760297-G-T

2361536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74760293-G-A

2361536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74760293-G-T

http://identifiers.org/hco/17/GRCh38#2361845-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74759796-A-C

2361845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74759796-A-G

2361931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74759737-G-A

2361931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74759737-G-T

http://identifiers.org/hco/17/GRCh38#2361975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74759681-C-A

2361975-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74759681-C-G

2361975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74759681-C-T

http://identifiers.org/hco/17/GRCh38#2362037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74759632-C-A

2362037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74759632-C-T

2362047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74759622-G-A

2362047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74759622-G-T

2362055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74759614-T-C

2362058-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74759611-G-C

2362058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74759611-G-T

2362171-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 74759500-C-G

2362171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 74759500-C-T

2362772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74759184-G-T

http://identifiers.org/hco/17/GRCh38#2362967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74758972-C-A

2362967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 74758972-C-T

http://identifiers.org/hco/17/GRCh38#2363286-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74758709-C-A

2363309-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74758686-G-C

2363405-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74758625-T-A

2363405-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74758625-T-G

2363434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74758600-G-T

2363492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, missense_variant, synonymous_variant
orthologous variants: 74758542-G-A

2363492-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, missense_variant, synonymous_variant
orthologous variants: 74758542-G-C

2363538-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 74758496-C-G

2363538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 74758496-C-T

http://identifiers.org/hco/17/GRCh38#2363728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74758342-C-A

2363728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74758342-C-T

2363743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74758329-A-G

2363800-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74758225-A-T

2363815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74758210-G-T

2363853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74758175-A-G

2363896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74758128-A-G

2363899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74758125-G-T

http://identifiers.org/hco/17/GRCh38#2363926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74758092-C-A

2363926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74758092-C-T

http://identifiers.org/hco/17/GRCh38#2363965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74758052-C-A

2364001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 74758030-C-T

2364219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74757820-C-T

2364366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74757668-G-A

2364366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74757668-G-T

2364468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74757570-G-A

2364483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74757555-A-G

http://identifiers.org/hco/17/GRCh38#2364709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74757349-C-A

2364836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74756430-G-A

2364863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74756390-G-T

http://identifiers.org/hco/17/GRCh38#2365160-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74756087-A-C

2365168-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74756079-T-G

http://identifiers.org/hco/17/GRCh38#2365182-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74756065-A-C

2365182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74756065-A-G

2365182-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74756065-A-T

2365209-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 74756041-C-G

2365264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 74755986-A-G

2365266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74755984-A-G

2365266-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74755984-A-T

http://identifiers.org/hco/17/GRCh38#2365293-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74755957-A-C

2365293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74755957-A-G

2365293-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74755957-A-T

2365355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74755898-G-A

2365355-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74755898-G-C

2365355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74755898-G-T

http://identifiers.org/hco/17/GRCh38#2365359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74755894-C-A

2365359-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74755894-C-G

2365532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 74755778-T-C

2365571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 74755744-T-C

2365599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 74755716-C-T

2365640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74755676-A-G

2366107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74755492-A-G

http://identifiers.org/hco/17/GRCh38#2366243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74755414-C-A

2366510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74755156-G-A

http://identifiers.org/hco/17/GRCh38#2366521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74755145-C-A

2366521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74755145-C-T

http://identifiers.org/hco/17/GRCh38#2366608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74755063-C-A

2366608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74755063-C-T

2366729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74754962-G-A

2366729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74754962-G-T

2366757-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74754936-C-G

2366757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74754936-C-T

2367079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74754706-G-A

2367079-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74754706-G-C

http://identifiers.org/hco/17/GRCh38#2367141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74754648-C-A

2367141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74754648-C-T

http://identifiers.org/hco/17/GRCh38#2367373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: http://identifiers.org/mco/11/GRCm39#74754416-C-A

2367373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74754416-C-T

http://identifiers.org/hco/17/GRCh38#2367432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74754357-C-A

2367462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74754324-G-A

2367462-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74754324-G-C

2367462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74754324-G-T

2367513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74754273-T-C

2367514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74754272-G-A

2367514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74754272-G-T

2367897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74753921-G-A

2367897-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74753921-G-C

2368003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74753821-A-G

2368039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74753787-G-A

2368212-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74753606-T-G

2368508-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74753312-C-G

http://identifiers.org/hco/17/GRCh38#2368589-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74753232-A-C

2368605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74753217-C-T

2368807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74753054-T-C

2368819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74753040-G-A

2368819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74753040-G-T

2369118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74752662-G-A

2369485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74752301-C-T

http://identifiers.org/hco/17/GRCh38#2369678-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74752094-A-C

2369766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74751992-C-T

2370311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74751512-G-A

2370369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74751454-G-A

2370369-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74751454-G-C

2370564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74751263-A-G

http://identifiers.org/hco/17/GRCh38#2370864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74751078-C-A

2371216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74750769-G-A

2371216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74750769-G-T

2371224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74750761-G-A

2371224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74750761-G-T

2371268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 74750717-G-A

2371268-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74750717-G-C

http://identifiers.org/hco/17/GRCh38#2371504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74750485-C-A

2371504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74750485-C-T

2371531-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74750457-G-C

2371531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74750457-G-T

2371533-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74750455-T-G

2371546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74750442-T-C

2371546-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74750442-T-G

2371576-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74750290-T-G

2371580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74750286-G-A

http://identifiers.org/hco/17/GRCh38#2371595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74750267-C-A

2371603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74750259-T-C

2371603-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74750259-T-G

2371613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74750249-C-T

http://identifiers.org/hco/17/GRCh38#2371712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74750168-C-A

2371712-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74750168-C-G

2371712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74750168-C-T

2371714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74750166-G-A

2371714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74750166-G-T

2371728-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74750151-T-A

2371728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74750151-T-C

2371728-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74750151-T-G

http://identifiers.org/hco/17/GRCh38#2371734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74750145-C-A

2371734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74750145-C-T

2371743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74750139-T-C

2371743-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74750139-T-G

2371748-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74750134-T-A

2371748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74750134-T-C

2371748-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74750134-T-G

2371800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74750083-A-G

2371814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74750074-G-A

2371881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74750002-G-A

2371881-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74750002-G-C

2371881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74750002-G-T

2371946-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74749942-T-A

2371946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74749942-T-C

2371946-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74749942-T-G

2372091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74749842-T-C

2372092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74749841-G-A

2372092-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74749841-G-C

2372095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74749838-T-C

http://identifiers.org/hco/17/GRCh38#2372115-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74749811-A-C

2372242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74749697-G-A

2372248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74749691-T-C

2372315-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74749617-T-G

2372539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74749400-G-A

2372539-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74749400-G-C

2372539-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74749400-G-T

http://identifiers.org/hco/17/GRCh38#2372553-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74749362-A-C

2372553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74749362-A-G

2372575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74749340-G-A

http://identifiers.org/hco/17/GRCh38#2372680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74749258-C-A

2372680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74749258-C-T

http://identifiers.org/hco/17/GRCh38#2372749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74749193-C-A

2372749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74749193-C-T

http://identifiers.org/hco/17/GRCh38#2372776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74749174-C-A

2372776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74749174-C-T

2372794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74749157-G-T

2372943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74749013-G-A

2372943-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74749013-G-C

2372959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74748997-A-G

2373020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74748936-A-G

2373034-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74748922-C-G

2373034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 74748922-C-T

2373144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74748811-A-G

http://identifiers.org/hco/17/GRCh38#2373159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74748797-C-A

2373159-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74748797-C-G

http://identifiers.org/hco/17/GRCh38#2373171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74748786-C-A

2373237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74748711-A-G

2373298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74748657-T-C

2373460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74748495-A-G

2373481-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74748474-C-G

2373683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74748275-G-A

2373683-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74748275-G-C

2373683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74748275-G-T

2373799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74748183-A-G

http://identifiers.org/hco/17/GRCh38#2373814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74748168-C-A

2373851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74748140-A-G

2373857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74748134-G-A

2373857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74748134-G-T

2373882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74748109-C-T

2373886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74748105-T-C

2373989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74748015-C-T

2374081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74747945-G-A

2374081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74747945-G-T

2374085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74747939-A-G

http://identifiers.org/hco/17/GRCh38#2374087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74747937-C-A

2374123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74747896-G-T

2374127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74747892-T-C

2374693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron variant
orthologous variants: 74746621-T-C

2374707-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron variant
orthologous variants: 74746607-T-A

2374707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron variant
orthologous variants: 74746607-T-C

2374707-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron variant
orthologous variants: 74746607-T-G

http://identifiers.org/hco/17/GRCh38#2374724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74746579-C-A

2374822-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron variant
orthologous variants: 74746473-A-T

2374965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron variant
orthologous variants: 74746347-T-C

2375054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron variant
orthologous variants: 74746276-A-G

2375054-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron variant
orthologous variants: 74746276-A-T

2375068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74746262-G-T

http://identifiers.org/hco/17/GRCh38#2375073-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74746260-A-C

2375073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74746260-A-G

2375073-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74746260-A-T

http://identifiers.org/hco/17/GRCh38#2375090-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74746243-A-C

2375090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74746243-A-G

2375090-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74746243-A-T

http://identifiers.org/hco/17/GRCh38#2375135-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74746201-A-C

2375135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74746201-A-G

http://identifiers.org/hco/17/GRCh38#2375138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74746198-C-A

2375138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74746198-C-T

http://identifiers.org/hco/17/GRCh38#2375248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74745532-C-A

2375248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74745532-C-T

http://identifiers.org/hco/17/GRCh38#2375268-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74745521-A-C

2375268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74745521-A-G

2375286-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74745510-T-A

2375286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74745510-T-C

2375286-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74745510-T-G

2375292-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74745504-T-A

2375292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74745504-T-C

2375292-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74745504-T-G

2375301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74745495-G-A

2375301-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74745495-G-T

2375366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74745433-T-C

2375450-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74745375-G-T

2375492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 74745333-G-A

2375492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 74745333-G-T

2375512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 74745313-T-C

2375542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 74745283-A-G

2375580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74745245-G-A

2375593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 74745232-C-T

2375594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74745231-G-A

2375621-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74745207-G-C

2375726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 74745102-G-A

2375809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 74745022-G-A

2375809-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 74745022-G-C

http://identifiers.org/hco/17/GRCh38#2375813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74745018-C-A

2375813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 74745018-C-T

2375844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 74744984-A-G

2375847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 74744981-T-C

http://identifiers.org/hco/17/GRCh38#2375937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74744909-C-A

2375937-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74744909-C-G

2375963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74744883-G-T

http://identifiers.org/hco/17/GRCh38#2375995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74744854-C-A

2375995-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74744854-C-G

2376079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74744790-G-A

2376262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 74744609-G-A

2376262-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 74744609-G-T

2376390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74744513-G-T

2376447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74744492-A-G

2376448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74744491-G-T

2376469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74744471-T-C

http://identifiers.org/hco/17/GRCh38#2376497-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74744456-A-C

2376497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74744456-A-G

2376497-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74744456-A-T

2376554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74744403-T-C

http://identifiers.org/hco/17/GRCh38#2376577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74744385-C-A

2376577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74744385-C-T

http://identifiers.org/hco/17/GRCh38#2376578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74744384-C-A

2376578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74744384-C-T

2376593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74744369-G-A

2376593-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74744369-G-C

2376593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74744369-G-T

http://identifiers.org/hco/17/GRCh38#2376608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74744355-C-A

2376608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74744355-C-T

2376632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74744327-T-C

2376651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74744308-G-A

2376651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74744308-G-T

2376746-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74744218-C-G

2376834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74744118-T-C

2376868-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74744090-G-C

2376868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74744090-G-T

2376887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74744075-G-A

2376908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74744054-T-C

http://identifiers.org/hco/17/GRCh38#2376933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74744034-C-A

2376934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74744033-C-T

2377139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74743845-G-A

2377146-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74743838-T-A

http://identifiers.org/hco/17/GRCh38#2377150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74743834-C-A

2377209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74743786-G-A

2377209-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74743786-G-C

2377222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74743780-A-G

2377241-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74743761-T-A

2377241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74743761-T-C

2377241-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74743761-T-G

2377250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74743748-C-T

2377392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74743625-G-A

2377392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74743625-G-T

http://identifiers.org/hco/17/GRCh38#2377440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74743595-C-A

2377440-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74743595-C-G

2377440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74743595-C-T

2378775-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74742234-G-C

2378901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74742126-G-A

2378901-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74742126-G-C

2378901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74742126-G-T

http://identifiers.org/hco/17/GRCh38#2378903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74742124-C-A

2378903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74742124-C-T

2379301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 74741824-G-A

2379310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 74741815-C-T

2379576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74741560-C-T

http://identifiers.org/hco/17/GRCh38#2379600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74741532-C-A

2379600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74741532-C-T

http://identifiers.org/hco/17/GRCh38#2379767-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74741343-A-C

2379767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74741343-A-G

2379816-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74741294-T-A

2379816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74741294-T-C

2379854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74741246-G-A

2379854-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74741246-G-C

2379854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74741246-G-T

2379886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74741214-G-A

2379886-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74741214-G-C

http://identifiers.org/hco/17/GRCh38#2379963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74741139-C-A

2379963-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74741139-C-G

2380095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74741063-T-C

2380355-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74740807-G-C

2380355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74740807-G-T

2380413-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74740751-T-G

2380478-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74740691-T-A

2380478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74740691-T-C

2380478-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74740691-T-G

2380562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74740606-G-A

http://identifiers.org/hco/17/GRCh38#2380572-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74740596-A-C

2380573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74740595-C-T

2380580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74740588-G-A

2380580-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74740588-G-T

2380654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74740515-G-A

2380654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74740515-G-T

http://identifiers.org/hco/17/GRCh38#2380682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74740485-C-A

2380682-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74740485-C-G

2380682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74740485-C-T

http://identifiers.org/hco/17/GRCh38#2380689-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74740478-A-C

2380689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74740478-A-G

2380689-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74740478-A-T

2380748-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74740427-G-C

http://identifiers.org/hco/17/GRCh38#2380884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#74740294-C-A

2381004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29026
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74740138-C-T