28457818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32362578-G-A

28457882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32362622-T-C

28457883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32362623-C-T

28458014-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32362754-G-C

28458035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32362775-G-A

28462332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32377154-T-C

28462380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32377202-T-C

28463279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32377950-A-G

28463707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32378420-C-T

28463747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32378451-G-T

28463981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32378665-C-T

28463982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32378666-G-A

http://identifiers.org/hco/2/GRCh38#28464069-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32378745-A-C

28464214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32378875-A-G

28464262-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32378918-T-A

28464298-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32378948-C-G

28464299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32378949-A-G

28464366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32379048-T-C

28464429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32379111-G-A

28464518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32379211-G-A

28464569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32379273-G-A

http://identifiers.org/hco/2/GRCh38#28464570-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32379274-A-C

28465240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32380033-C-T

28465636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32381277-G-A

28465673-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32381313-A-T

28465691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32381331-G-A

28466393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32384039-T-C

http://identifiers.org/hco/2/GRCh38#28466394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32384040-C-A

28466394-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32384040-C-G

28466467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32384104-G-A

28466467-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32384104-G-C

28466813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32384362-C-T

28470358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32388906-C-T

28470448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32388994-C-T

28470822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32389385-T-C

28471134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32389651-C-T

28471135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32389652-G-A

28471789-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32390272-T-A

28471789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32390272-T-C

28471856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32390338-G-A

28471939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32390418-C-T

28471944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32390423-C-T

http://identifiers.org/hco/2/GRCh38#28472058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32390525-C-A

28472058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32390525-C-T

28472118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32390586-T-C

28472154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32390620-C-T

28472170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32390640-T-C

28472315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32390785-G-A

28476491-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32392316-G-C

28477169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32392886-C-T

28477193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32392902-A-G

28484301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32394447-A-G

28484406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32394544-C-T

28484817-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32394586-G-C

http://identifiers.org/hco/2/GRCh38#28485090-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32394829-A-C

28485221-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32394938-T-A

28485429-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32395120-A-T

28485738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32395408-T-C

28486901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32396327-A-G

28486901-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32396327-A-T

28487067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32396436-G-A

http://identifiers.org/hco/2/GRCh38#28488227-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32398102-A-C

28488227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32398102-A-G

28488227-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32398102-A-T

28488449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32398311-T-C

28488688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32398532-G-A

28488831-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32398718-C-G

28488875-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32398761-G-C

28488875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32398761-G-T

28489519-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32399328-T-A

http://identifiers.org/hco/2/GRCh38#28489676-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32399481-A-C

28489677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32399482-G-T

28489785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32399589-G-T

http://identifiers.org/hco/2/GRCh38#28489843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32399616-C-A

http://identifiers.org/hco/2/GRCh38#28489889-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32399653-C-A

28490176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32399945-G-A

28490176-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32399945-G-C

28490250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32400069-C-T

http://identifiers.org/hco/2/GRCh38#28490326-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32400140-A-C

28490490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32400267-G-A

28490490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32400267-G-T

28490552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32400340-G-A

28490552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32400340-G-T

28490612-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32400471-A-T

28491349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32401034-T-C

28491496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32401193-G-A

28491661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32401345-A-G

28493040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32401930-G-T

28493533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32402095-G-A

28493960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32402581-G-A

http://identifiers.org/hco/2/GRCh38#28493992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32402610-C-A

28494180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32402748-G-T

28494292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32402847-G-A

28494292-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32402847-G-C

28494442-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32402999-C-G

28494538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32403058-C-T

http://identifiers.org/hco/2/GRCh38#28494620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32403152-C-A

28494620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32403152-C-T

28494737-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32403251-A-T

28495752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32404503-G-A

28495804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32404548-C-T

28495926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32404666-T-C

28495963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32404703-C-T

http://identifiers.org/hco/2/GRCh38#28495964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32404704-C-A

28496002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32404742-G-A

28496002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32404742-G-T

28496106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32404835-C-T

28496125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, missense_variant
orthologous variants: 32404854-G-A

28496125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, missense_variant
orthologous variants: 32404854-G-T

28496219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32404934-T-C

http://identifiers.org/hco/2/GRCh38#28496223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32404938-C-A

28496615-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32405396-G-T

http://identifiers.org/hco/2/GRCh38#28496736-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32405504-A-C

28496768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32405530-T-C

28497038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32405720-C-T

http://identifiers.org/hco/2/GRCh38#28497055-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32405739-A-C

28497159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32405819-A-G

28504272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32410431-C-T

http://identifiers.org/hco/2/GRCh38#28504962-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32410913-A-C

28505128-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32411355-T-A

28505288-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32411508-A-T

28505602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32411894-T-C

28505607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32411899-G-A

28505616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32411996-A-G

http://identifiers.org/hco/2/GRCh38#28505624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32412013-C-A

28505624-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32412013-C-G

28505630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32412019-A-G

28505843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32412224-C-T

28506043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32412400-T-C

28506245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32412591-G-A

28506245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32412591-G-T

28506943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32412953-A-G

28506945-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32412958-T-A

28507058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32413100-A-G

28507671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32413169-C-T

28507699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32413197-A-G

28507779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32413269-A-G

http://identifiers.org/hco/2/GRCh38#28508148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32413964-C-A

28508227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32414025-G-A

28508227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32414025-G-T

http://identifiers.org/hco/2/GRCh38#28508288-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32414082-A-C

28508288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32414082-A-G

28508288-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32414082-A-T

28508750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32414517-T-C

28508923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32414699-T-C

28509099-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32414866-T-G

28509100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32414867-A-G

28509246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32415002-G-A

28509257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32415013-C-T

28509375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32415126-G-A

http://identifiers.org/hco/2/GRCh38#28509394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32415145-C-A

28509451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32415208-C-T

http://identifiers.org/hco/2/GRCh38#28509461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32415218-C-A

28509537-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32415305-T-G

http://identifiers.org/hco/2/GRCh38#28509727-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32415489-A-C

28509766-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32415527-G-C

28509773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32415534-G-T

28509880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32415649-G-A

28509967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32415734-G-T

28510022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32415782-A-G

28510038-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32415797-T-A

28510151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32415932-C-T

28514401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32417406-A-G

http://identifiers.org/hco/2/GRCh38#28514429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32417434-C-A

28514429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32417434-C-T

28514620-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32417638-T-A

http://identifiers.org/hco/2/GRCh38#28514692-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32417714-A-C

28514762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32417784-A-G

28515101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32417968-G-A

28515101-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32417968-G-T

28515175-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32418041-A-T

28515303-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32418166-G-C

28515375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32418225-C-T

28515576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32418397-T-C

28516356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32418952-A-G

http://identifiers.org/hco/2/GRCh38#28516748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32419355-C-A

28516789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32419671-T-C

28516897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32419796-G-A

28516897-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32419796-G-C

28516897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32419796-G-T

28516910-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32419847-G-C

28516989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32419929-G-A

28517007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32419947-G-A

28517007-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32419947-G-C

28517007-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32419947-G-T

28517259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32420200-A-G

28517588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32420510-A-G

28517672-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32420567-A-T

28518236-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32420792-G-C

28518271-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32420829-G-C

28518298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32420856-A-G

28518496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 32421054-C-T

http://identifiers.org/hco/2/GRCh38#28518549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32421107-C-A

28518549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32421107-C-T

28518602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32421144-A-G

28518791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32421481-G-A

28518811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32421501-A-G

28518830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32421521-A-G

28519096-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32421739-G-T

28519507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32422061-G-A

28519579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32422119-A-G

28519647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32422193-G-A

28519686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32422226-T-C

28519786-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32422325-G-C

28519826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32422363-G-A

28519826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32422363-G-T

http://identifiers.org/hco/2/GRCh38#28519852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32422389-C-A

28519852-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32422389-C-G

28520261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32422618-C-T

28520262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32422619-C-T

http://identifiers.org/hco/2/GRCh38#28520317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32422673-C-A

28523916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32426101-C-T

28524043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32426239-G-A

28524165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32426342-C-T

28524225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32426410-T-C

http://identifiers.org/hco/2/GRCh38#28524281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32426548-C-A

28525316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32427202-C-T

28525317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32427203-C-T

28525381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32427264-T-C

28525381-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32427264-T-G

28525382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32427265-G-A

28525382-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32427265-G-C

28525382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32427265-G-T

28525454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32427325-C-T

http://identifiers.org/hco/2/GRCh38#28525509-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32427372-A-C

28525537-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32427401-G-C

28525640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32427496-A-G

28525673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32427528-C-T

28525676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32427531-G-A

28525684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32427538-C-T

28525698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32427545-G-A

28525801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32427595-G-A

28525801-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32427595-G-C

28525816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32427610-A-G

28525816-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32427610-A-T

28525832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32427626-C-T

http://identifiers.org/hco/2/GRCh38#28525855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32427652-C-A

28525979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32427771-T-C

28526010-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32427802-T-A

28526010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32427802-T-C

28526067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32427859-G-A

28526067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32427859-G-T

28526120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32427917-A-G

28526318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32428061-C-T

28526503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32428253-G-T

28526747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32428427-G-A

28527318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32428921-C-T

28527744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32429330-G-A

28527751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32429337-G-A

28527914-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32429486-A-T

28528166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32429770-C-T

http://identifiers.org/hco/2/GRCh38#28528318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32429901-C-A

28528318-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32429901-C-G

28528607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32430116-A-G

http://identifiers.org/hco/2/GRCh38#28528634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32430143-C-A

28528634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32430143-C-T

28528770-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32430233-T-G

28528794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32430257-A-G

28528845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32430279-G-A

28528892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32430315-G-A

28528911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32430333-G-A

28529313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 32430387-T-C

28529313-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 32430387-T-G

28529426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32430500-T-C

28529481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32430549-G-A

28529481-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32430549-G-C

28529481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32430549-G-T

28529620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32430684-T-C

28529620-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32430684-T-G

28529624-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32430691-T-A

28529624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32430691-T-C

http://identifiers.org/hco/2/GRCh38#28529629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32430696-C-A

28529629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32430696-C-T

28529811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32430870-G-A

28529814-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32430873-G-C

28529814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32430873-G-T

28529854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32430920-G-T

28529889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32430937-A-G

28532325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32433652-G-A

28532325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32433652-G-T

28532345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32433672-G-T

28532410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32433736-G-T

28532549-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32433887-T-A

28532603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32433942-A-G

28532684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32435053-G-A

28532684-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32435053-G-C

28532733-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32435182-G-C

28532790-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32435240-G-C

28532823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32435284-T-C

28532828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32435289-C-T

28532851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32435305-G-A

28532853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32435307-G-A

28532966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32435424-C-T

28533292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32435729-G-T

28533388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32435805-A-G

28533463-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32435874-G-C

28533482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32435897-G-T

28533484-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32435899-T-G

28533680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32436011-T-C

28533911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32436245-C-T

28534141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32436393-A-G

28534152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32436404-T-C

28534166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32436418-A-G

28534224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32436476-C-T

28534240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32436484-T-C

28534373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32436581-C-T

28534551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32436762-G-T

28536849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32436852-C-T

28537040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32437051-A-G

28537135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32437114-C-T

28537173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32437144-C-T

28537429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32437435-A-G

28537447-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32437467-T-A

28537447-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32437467-T-G

28537457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32437475-G-A

28537952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32438112-G-A

http://identifiers.org/hco/2/GRCh38#28538149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32438290-C-A

28538149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32438290-C-T

http://identifiers.org/hco/2/GRCh38#28538223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32438359-C-A

28538223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32438359-C-T

28538249-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32438374-T-G

28538308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, missense_variant
orthologous variants: 32438432-T-C

28538331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: missense variant
orthologous variants: 32438455-G-A

28538331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: missense variant
orthologous variants: 32438455-G-T

28538392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32438516-G-A

28538392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32438516-G-T

28538413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32438534-G-A

28538731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32438803-A-G

28538751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32438823-G-T

28538763-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32438834-C-G

28538763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32438834-C-T

28538764-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32438835-C-G

http://identifiers.org/hco/2/GRCh38#28538970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32438977-C-A

28538970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32438977-C-T

28539151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: missense variant
orthologous variants: 32439131-C-T

28539823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32440450-G-A

28539823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32440450-G-T

28540196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32442045-C-T

28540452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32442312-C-T

28540464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32442323-A-G

28541395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32442859-C-T

http://identifiers.org/hco/2/GRCh38#28541570-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32443033-A-C

28541570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32443033-A-G

28541570-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32443033-A-T

28541587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32443039-T-C

28541587-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32443039-T-G

28541724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: synonymous variant
orthologous variants: 32443164-C-T

28542327-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32443475-C-G

28542327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32443475-C-T

28542498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32443624-C-T

28542763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32443749-C-T

28543033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32443981-G-A

28543081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32444025-G-A

28543085-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32444028-T-G

28543086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32444029-G-A

28543086-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32444029-G-T

http://identifiers.org/hco/2/GRCh38#28543103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32444046-C-A

28543103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32444046-C-T

28543127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32444062-G-A

28543127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32444062-G-T

http://identifiers.org/hco/2/GRCh38#28543217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32444153-C-A

28543217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: synonymous variant
orthologous variants: 32444153-C-T

28543282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32444216-G-T

http://identifiers.org/hco/2/GRCh38#28543691-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32444379-A-C

28543691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32444379-A-G

http://identifiers.org/hco/2/GRCh38#28543770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32444457-C-A

28543982-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32444631-A-T

28543989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32444641-A-G

28544019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32444671-T-C

28544238-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32444902-G-C

28544267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32444954-G-A

28544267-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32444954-G-C

28544329-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32445285-A-T

28544433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32445391-C-T

28544925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32445630-C-T

28548303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32446656-A-G

28548327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32446680-T-C

28548420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32446758-A-G

http://identifiers.org/hco/2/GRCh38#28548425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32446762-C-A

28548425-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32446762-C-G

28548425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32446762-C-T

28548432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32446769-G-A

28548432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32446769-G-T

28548448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32446785-G-T

28548474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32446810-G-A

http://identifiers.org/hco/2/GRCh38#28548518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32446845-C-A

28548518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 32446845-C-T

28548730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32447052-G-A

28548730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32447052-G-T

28548868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: synonymous variant
orthologous variants: 32447191-A-G

28548892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: synonymous variant
orthologous variants: 32447215-G-A

28548896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: missense variant
orthologous variants: 32447219-G-A

28549106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32447420-C-T

28549861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32447956-G-A

28549883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32447977-G-A

28549883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32447977-G-T

28549950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32448499-G-T

http://identifiers.org/hco/2/GRCh38#28549965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32448514-C-A

28549965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32448514-C-T

http://identifiers.org/hco/2/GRCh38#28550018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32448562-C-A

28550161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32448694-T-C

28550161-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32448694-T-G

28551160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32448955-G-A

28551165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32448960-G-A

28551214-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32449021-T-G

28551396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32449196-G-A

28551489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32449268-G-A

28551753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32449508-C-T

28551770-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32449521-T-G

28552818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32450439-A-G

28552840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32450467-A-G

28552856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32450483-A-G

28552996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32450624-A-G

28553006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32450638-C-T

28553081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32450709-G-A

28553081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32450709-G-T

28553116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32450763-A-G

http://identifiers.org/hco/2/GRCh38#28553264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32450904-C-A

28553475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32451263-G-A

http://identifiers.org/hco/2/GRCh38#28553617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32451410-C-A

28553633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32451426-G-A

28553960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32451723-C-T

http://identifiers.org/hco/2/GRCh38#28553965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32451728-C-A

28554763-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32452809-C-G

28554763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32452809-C-T

28555089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32453118-C-T

28556320-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32453695-T-G

28556707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32454029-A-G

28558055-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32454438-T-A

28558122-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32454494-A-T

28558180-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32454589-G-C

28558242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32454727-T-C

28558376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32454877-G-A

28558869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32455337-C-T

28559382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32455588-A-G

28563052-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: stop gained
orthologous variants: 32455874-A-T

28563057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: synonymous variant
orthologous variants: 32455879-G-A

28563057-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: synonymous variant
orthologous variants: 32455879-G-C

28563057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: synonymous variant
orthologous variants: 32455879-G-T

28563491-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32456402-C-G

28564937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32459668-T-C

28565068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32459796-C-T

http://identifiers.org/hco/2/GRCh38#28565105-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32459812-A-C

28565130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32459837-A-G

28565202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32459901-A-G

http://identifiers.org/hco/2/GRCh38#28565204-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32459903-A-C

28565291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: synonymous variant
orthologous variants: 32459991-G-A

28565298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: missense variant
orthologous variants: 32459998-T-C

http://identifiers.org/hco/2/GRCh38#28565378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32460065-C-A

28565378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32460065-C-T

28565451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32460105-G-T

28565452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32460106-G-T

28565471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32460118-A-G

28565473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron variant
orthologous variants: 32460120-G-T

http://identifiers.org/hco/2/GRCh38#28566506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32460389-C-A

28566514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32460397-A-G

28566523-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32460406-T-G

http://identifiers.org/hco/2/GRCh38#28566568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32460473-C-A

28566568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32460473-C-T

http://identifiers.org/hco/2/GRCh38#28566613-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32460519-A-C

28566613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32460519-A-G

28566613-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32460519-A-T

28566640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32460541-G-A

28566640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32460541-G-T

28566665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32460551-G-A

28566665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32460551-G-T

28566694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 32460574-G-A

28566694-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 32460574-G-C

28566694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 32460574-G-T

28566832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 32460687-C-T

http://identifiers.org/hco/2/GRCh38#28566914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#32460759-C-A

28566914-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32460759-C-G

28566914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32460759-C-T

28567228-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32461034-C-G

28567228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32461034-C-T

28567287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32461060-C-T

28567290-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32461063-C-G

28567290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32461063-C-T

28567459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32461220-A-G

28567459-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32461220-A-T

28567978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32461717-T-C

28567980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32461719-T-C

28568202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32461954-T-C

28568259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32462009-C-T

28568762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32462445-C-T

28573368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32464082-G-T

28573406-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32464122-G-C

28573406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32464122-G-T

28573413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32464129-G-T

28573609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32464321-C-T

28573645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32464351-C-T

28573836-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32464537-G-C

28575418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32464823-A-G

28575972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32465063-G-A

28576076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32465169-T-C

28576181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32465250-G-T

28576408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32465472-G-A

28576408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32465472-G-T

28576430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32465493-A-G

http://identifiers.org/hco/2/GRCh38#28576716-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32465527-C-A

28576716-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32465527-C-G

28576716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32465527-C-T

28576798-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32465564-C-G

28576907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32465663-C-T

28577096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32465811-C-T

http://identifiers.org/hco/2/GRCh38#28577098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32465813-C-A

28577175-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32465876-G-C

28577195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32465896-G-A

28577233-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32465933-C-G

28577247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32465947-T-C

28577251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32465951-G-T

28577258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32465980-G-T

http://identifiers.org/hco/2/GRCh38#28577328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32466056-C-A

28577437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32466175-T-C

28577892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32466318-C-T

28577936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32466352-G-A

28577936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32466352-G-T

28577973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32466389-G-A

28577973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32466389-G-T

28578000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32466404-G-A

28578000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32466404-G-T

http://identifiers.org/hco/2/GRCh38#28578020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32466418-C-A

28578109-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 32466510-A-T

28578118-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32466519-T-A

http://identifiers.org/hco/2/GRCh38#28578119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32466520-C-A

28578119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32466520-C-T

28578138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32466539-G-T

28578273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32466678-G-A

28578299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32466705-G-A

28578347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32466723-T-C

28578431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32466797-C-T

28578530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32466894-T-C

28578995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32467284-C-T

28579026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32467308-T-C

28579027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32467309-G-A

28579702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32468257-G-A

28579702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32468257-G-T

28579766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32468306-G-A

http://identifiers.org/hco/2/GRCh38#28579776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32468312-C-A

28579839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32468374-G-A

28579839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32468374-G-T

28579908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32468411-A-G

http://identifiers.org/hco/2/GRCh38#28582017-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32470957-A-C

28582017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32470957-A-G

28582038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32470978-G-A

28582038-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32470978-G-C

28582092-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 32471032-A-T

http://identifiers.org/hco/2/GRCh38#28582267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32471206-C-A

28582267-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32471206-C-G

28582267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32471206-C-T

28582301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32471243-G-A

28582331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32471278-A-G

http://identifiers.org/hco/2/GRCh38#28582363-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32471299-C-A

28582363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32471299-C-T

http://identifiers.org/hco/2/GRCh38#28582374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32471310-C-A

28582374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32471310-C-T

28582464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32471398-G-A

28582464-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32471398-G-C

28582464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32471398-G-T

28582483-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32471417-T-G

http://identifiers.org/hco/2/GRCh38#28582572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32471488-C-A

28582572-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32471488-C-G

28582572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32471488-C-T

28582573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32471489-A-G

http://identifiers.org/hco/2/GRCh38#28582612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32471529-C-A

28582612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32471529-C-T

http://identifiers.org/hco/2/GRCh38#28582622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32471539-C-A

28582622-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32471539-C-G

28582622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32471539-C-T

28582786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32471698-G-A

28583061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32471931-G-A

28583086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32471962-C-T

28584038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32472063-C-T

28584442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32472446-A-G

28584453-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32472457-T-G

http://identifiers.org/hco/2/GRCh38#28584513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32472538-C-A

28584690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32472683-C-T

http://identifiers.org/hco/2/GRCh38#28585815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32473989-C-A

28585815-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32473989-C-G

28585815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32473989-C-T

28585819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32473993-A-G

http://identifiers.org/hco/2/GRCh38#28589435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32474353-C-A

28589435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32474353-C-T

28589491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32474409-A-G

28589565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32474483-C-T

28589650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32474547-C-T

28589691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32474588-A-G

28589692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32474589-C-T

28589784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32474677-G-A

28589900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32474704-C-T

28589965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32474765-G-A

28589965-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32474765-G-C

28589965-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32474765-G-T

28589981-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32474781-C-G

28590034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32474838-T-C

28590170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32474970-G-A

28590170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32474970-G-T

http://identifiers.org/hco/2/GRCh38#28590174-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32474974-A-C

28590174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32474974-A-G

28590174-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32474974-A-T

http://identifiers.org/hco/2/GRCh38#28590178-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32474978-A-C

http://identifiers.org/hco/2/GRCh38#28590181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32474981-C-A

28590181-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32474981-C-G

28590181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32474981-C-T

28590202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32475000-A-G

28590223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32475021-G-A

28590612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32475404-T-C

28590617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32475409-G-A

28590713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32475517-C-T

28590737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32475541-G-A

28590946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32475709-G-T

http://identifiers.org/hco/2/GRCh38#28591119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32475863-C-A

28591119-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32475863-C-G

28591119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32475863-C-T

28591210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32475954-G-A

28591488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32476155-G-A

28591602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32476236-G-T

http://identifiers.org/hco/2/GRCh38#28591643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32476265-C-A

28591643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32476265-C-T

28591678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32476312-G-A

28591678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32476312-G-T

http://identifiers.org/hco/2/GRCh38#28591693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32476327-C-A

28591693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 32476327-C-T

28591704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32476338-A-G

28591704-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32476338-A-T

http://identifiers.org/hco/2/GRCh38#28591877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32476898-C-A

28591877-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32476898-C-G

28591877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32476898-C-T

http://identifiers.org/hco/2/GRCh38#28591897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32476906-C-A

28591897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32476906-C-T

28591943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32476941-A-G

28592367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32477362-C-T

28592410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32477389-T-C

28592506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32477473-T-C

28592686-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32477649-C-G

http://identifiers.org/hco/2/GRCh38#28592829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32477799-C-A

28592829-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32477799-C-G

28592829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32477799-C-T

28592896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32477876-T-C

28592906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32477886-A-G

http://identifiers.org/hco/2/GRCh38#28593565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32478522-C-A

28593591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32478548-G-A

28593591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32478548-G-T

28593857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32478915-T-C

28594421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32479603-G-A

28594421-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32479603-G-C

28594421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32479603-G-T

28594677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32479839-G-A

http://identifiers.org/hco/2/GRCh38#28594768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32479918-C-A

28594768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32479918-C-T

http://identifiers.org/hco/2/GRCh38#28594838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32479987-C-A

28594940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32480098-G-A

http://identifiers.org/hco/2/GRCh38#28595044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32480177-C-A

28595044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32480177-C-T

28595047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32480180-G-T

28595100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32480218-C-T

http://identifiers.org/hco/2/GRCh38#28595110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32480232-C-A

http://identifiers.org/hco/2/GRCh38#28595163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32480278-C-A

28595163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32480278-C-T

28595306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32480410-T-C

28595430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32480524-A-G

28595517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32480589-G-A

28595943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32481011-G-T

28595972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32481179-G-A

28595972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32481179-G-T

28596506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32481688-G-A

28597289-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-G

28597290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-T

28597307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

28597410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32482209-C-T

28597521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32482318-C-T

28597665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32482455-G-A

28597763-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32482551-T-G

http://identifiers.org/hco/2/GRCh38#28597853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32482638-C-A

28597853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32482638-C-T

28598018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32482750-G-A

28598018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32482750-G-T

28598032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32482764-T-C

28598032-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32482764-T-G

28598250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32482929-C-T

28598275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-T

28598698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32483489-C-T

28598712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32483503-A-G

28598712-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32483503-A-T

28598718-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32483509-C-G

28598718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32483509-C-T

28598727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32483518-T-C

28598727-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32483518-T-G

http://identifiers.org/hco/2/GRCh38#28598786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32483569-C-A

28598934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32483710-G-T

28598960-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32483742-C-G

28599051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32483839-A-G

28599404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32484141-C-T

28599426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32484162-G-A

28600679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32485210-C-T

28600686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32485217-T-C

28600686-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32485217-T-G

http://identifiers.org/hco/2/GRCh38#28600744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32485273-C-A

28600744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32485273-C-T

28600780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32485309-C-T

28600853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32485379-A-G

http://identifiers.org/hco/2/GRCh38#28600953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32485468-C-A

28600998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32485512-G-A

28600998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32485512-G-T

28601005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32485519-G-A

28601005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32485519-G-T

28601052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32485566-A-G

http://identifiers.org/hco/2/GRCh38#28601095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32485607-C-A

28601095-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32485607-C-G

28601279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32485783-G-A

28601325-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32485829-C-G

28601435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32485938-T-C

http://identifiers.org/hco/2/GRCh38#28601513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32486004-C-A

28601716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32486187-A-G

http://identifiers.org/hco/2/GRCh38#28601818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32486288-C-A

28601818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32486288-C-T

28602002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32486474-G-A

28602002-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32486474-G-C

28602074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32486524-G-T

28602534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32486925-G-A

http://identifiers.org/hco/2/GRCh38#28602670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32487065-C-A

28602729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32487125-G-T

28602880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32487251-G-A

28602880-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32487251-G-C

http://identifiers.org/hco/2/GRCh38#28602946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32487316-C-A

28602946-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32487316-C-G

28602946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32487316-C-T

28602969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32487338-G-T

28602970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32487339-G-A

28602970-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32487339-G-C

28603072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32487415-A-G

28603740-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32487705-G-C

28603911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32487852-A-G

28603960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 32487902-G-A

28603972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 32487914-G-A

28603972-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 32487914-G-C

28603972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 32487914-G-T

http://identifiers.org/hco/2/GRCh38#28604186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32488074-C-A

28604186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32488074-C-T

28604274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32488163-A-G

28604299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32488203-A-G

28604338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32488255-T-C

28604480-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32488434-T-A

28604549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32488502-G-A

28604549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32488502-G-T

28604639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32488570-G-A

http://identifiers.org/hco/2/GRCh38#28604767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32488699-C-A

28604795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32488723-G-T

28604823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32488777-G-A

28604823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32488777-G-T

28604824-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32488778-T-G

28604857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32488810-G-T

28605021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32488904-C-T

28605199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32489073-G-A

28605199-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32489073-G-C

28605690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32490010-G-A

28605690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32490010-G-T

http://identifiers.org/hco/2/GRCh38#28605744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32490029-C-A

28605744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32490029-C-T

http://identifiers.org/hco/2/GRCh38#28605775-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32490059-A-C

28605775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32490059-A-G

28605777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32490061-T-C

http://identifiers.org/hco/2/GRCh38#28605816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32490097-C-A

28605995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32490263-G-A

28606031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32490289-G-A

28606031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32490289-G-T

http://identifiers.org/hco/2/GRCh38#28606071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32490329-C-A

28606071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32490329-C-T

http://identifiers.org/hco/2/GRCh38#28606095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32490353-C-A

28606095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32490353-C-T

28606112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32490368-C-T

28606247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32490588-C-T

http://identifiers.org/hco/2/GRCh38#28606358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32490671-C-A

28606358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32490671-C-T

28606564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32490842-T-C

http://identifiers.org/hco/2/GRCh38#28606623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32490883-C-A

28606623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32490883-C-T

http://identifiers.org/hco/2/GRCh38#28606641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32490904-C-A

28606641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32490904-C-T

http://identifiers.org/hco/2/GRCh38#28606656-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32490919-A-C

28606656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32490919-A-G

http://identifiers.org/hco/2/GRCh38#28606660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32490923-C-A

28606660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32490923-C-T

28606807-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32491038-C-G

28606807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32491038-C-T

28607320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32491471-C-T

28607380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32491542-G-A

28607586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32491663-C-T

28608004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32492393-C-T

28608085-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32492464-G-C

28608312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32492671-A-G

28608511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32492853-G-A

28608529-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32492872-G-C

28608544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32492887-C-T

28608545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32492888-G-A

28608634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32492974-C-T

28610972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32493711-T-C

28611214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32493783-T-C

28611455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32494003-T-C

28611471-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32494019-C-G

28613899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32495295-A-G

28613930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32495323-A-G

28613948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32495341-G-T

http://identifiers.org/hco/2/GRCh38#28614112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32495495-C-A

28614112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32495495-C-T

28614152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32495535-G-A

28614167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32495551-A-G

28614183-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32495565-T-A

http://identifiers.org/hco/2/GRCh38#28614243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#32495644-C-A

28614243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32495644-C-T

28614619-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32496026-G-C

28614819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32496178-G-A

28614819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32496178-G-T

28614846-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32496205-A-T

28615073-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32496451-A-T

http://identifiers.org/hco/2/GRCh38#28615150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32496543-C-A

28615150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32496543-C-T

28615564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32497107-G-A

28615789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32497312-C-T

28615822-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32497345-G-C

28617372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32498904-G-A

28617678-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32499205-C-G

28617678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32499205-C-T

28617827-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32499332-T-A

28617841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32499346-T-C

28617972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32499491-T-C

28618306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32499797-G-A

28618335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 32499817-C-T

28618415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32499897-T-C

28618480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32499948-G-T

28618481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32499949-G-A

28618481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32499949-G-T

28618536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32499971-G-T

http://identifiers.org/hco/2/GRCh38#28618562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32500003-C-A

28618562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32500003-C-T

http://identifiers.org/hco/2/GRCh38#28618586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32500037-C-A

28618586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32500037-C-T

28618951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32500330-C-T

28619869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32501660-G-A

28619869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32501660-G-T

28620184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32501902-T-C

http://identifiers.org/hco/2/GRCh38#28620186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32501904-C-A

28620186-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32501904-C-G

28620186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32501904-C-T

28620187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32501905-T-C

28620273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32502196-G-A

28620273-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32502196-G-C

28620273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32502196-G-T

28620293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32502216-C-T

28620294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32502217-C-T

28620300-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32502223-C-G

28620300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32502223-C-T

http://identifiers.org/hco/2/GRCh38#28620514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32502633-C-A

28620569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32502685-G-T

28620651-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 32502771-G-C

28620687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32502801-C-T

28620711-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32502825-G-C

28620855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32502960-T-C

28620867-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32502972-C-G

28620867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32502972-C-T

http://identifiers.org/hco/2/GRCh38#28620884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32502986-C-A

28620884-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32502986-C-G

28620888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32502990-A-G

http://identifiers.org/hco/2/GRCh38#28621076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32503164-C-A

28621094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32503203-G-A

28621094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32503203-G-T

28621108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32503217-A-G

28621108-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32503217-A-T

28621293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32503397-A-G

28621609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32503696-G-A

28621760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32503848-G-A

http://identifiers.org/hco/2/GRCh38#28621966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32504024-C-A

28622534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32505470-C-T

28623258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32505724-G-A

28623258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32505724-G-T

28623302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32505771-G-A

28623375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32505836-A-G

28623549-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32505975-C-G

28624569-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32506496-A-T

28624749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32506670-T-C

28625036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32506947-C-T

http://identifiers.org/hco/2/GRCh38#28625165-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32507061-A-C

28625165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32507061-A-G

28625167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32507063-G-A

28625358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32507210-G-A

28625586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32507409-G-A

28625807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32507593-G-A

28625932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32507709-T-C

28626418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32507872-G-A

28626418-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32507872-G-C

28626466-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32507920-C-G

28626466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32507920-C-T

28626633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32508075-G-A

28626633-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32508075-G-C

28626633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32508075-G-T

http://identifiers.org/hco/2/GRCh38#28626642-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32508084-C-A

28626642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32508084-C-T

28627266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32508689-T-C

http://identifiers.org/hco/2/GRCh38#28627290-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32508711-A-C

28627290-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32508711-A-T

28627317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32508737-G-A

28627459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32508883-G-A

http://identifiers.org/hco/2/GRCh38#28628730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32509185-C-A

28628730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32509185-C-T

http://identifiers.org/hco/2/GRCh38#28628944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32509391-C-A

28629015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32509456-G-A

28629015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32509456-G-T

28629028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32509468-G-A

28629028-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32509468-G-C

28629028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32509468-G-T

28629124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32509542-G-A

28629124-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32509542-G-T

28629195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32509616-C-T

http://identifiers.org/hco/2/GRCh38#28629248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32509657-C-A

http://identifiers.org/hco/2/GRCh38#28629267-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32509676-A-C

28629267-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32509676-A-T

28629269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32509678-G-A

28629269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32509678-G-T

28629421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32509793-A-G

28629633-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32509972-A-T

28629765-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32510066-G-C

28629781-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32510077-T-G

28630324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32510749-G-A

28630547-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32510931-G-C

28630547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32510931-G-T

http://identifiers.org/hco/2/GRCh38#28630718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32511113-C-A

28630718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32511113-C-T

28630719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32511114-A-G

28631324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32511482-C-T

http://identifiers.org/hco/2/GRCh38#28631462-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32511605-A-C

28631462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32511605-A-G

28631553-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32511697-G-C

28631845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32511957-C-T

28631943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32512046-A-G

28631943-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32512046-A-T

28631949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32512052-G-A

28631949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32512052-G-T

28632167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32512261-T-C

28632615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32512500-C-T

28632794-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32512526-T-A

28632796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32512528-G-T

http://identifiers.org/hco/2/GRCh38#28632926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32512643-C-A

28632926-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32512643-C-G

28633054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32512771-G-A

28633054-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32512771-G-C

http://identifiers.org/hco/2/GRCh38#28633182-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32512868-A-C

28633182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32512868-A-G

http://identifiers.org/hco/2/GRCh38#28633206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32513381-C-A

28633206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32513381-C-T

28633208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32513383-T-C

28633231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32513403-A-G

28633329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32513481-A-G

28633329-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32513481-A-T

28633377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32513516-G-A

28633377-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32513516-G-C

28633377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32513516-G-T

28633422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32513562-A-G

28633559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32513791-T-C

28633559-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32513791-T-G

28633765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32513976-A-G

http://identifiers.org/hco/2/GRCh38#28633772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32513983-C-A

28633772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32513983-C-T

28633881-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32514062-C-G

28633978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32514157-T-C

28635262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32515181-C-T

28635336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32515251-A-G

http://identifiers.org/hco/2/GRCh38#28635421-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32515328-A-C

28635542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32515431-G-A

28635748-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32515627-T-A

28635798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32515678-G-A

28639550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32518687-G-A

28640498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32519497-C-T

28640630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32519630-T-C

28640692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32519686-G-A

28640742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32519727-A-G

28640756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32519741-G-A

28640756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32519741-G-T

http://identifiers.org/hco/2/GRCh38#28640798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32519769-C-A

28640798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32519769-C-T

28640830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32519794-G-A

28640869-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32519831-G-C

http://identifiers.org/hco/2/GRCh38#28641018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32519968-C-A

28641018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32519968-C-T

http://identifiers.org/hco/2/GRCh38#28641086-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: -C-A

28641086-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: -C-G

28641086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

28641123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32520023-G-A

28641123-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32520023-G-C

28641123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32520023-G-T

28641690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32520486-A-G

28641999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32520764-G-A

28641999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32520764-G-T

28642222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32520914-T-C

28642320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32520996-C-T

28642835-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32521315-T-A

28642835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32521315-T-C

http://identifiers.org/hco/2/GRCh38#28642839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32521319-C-A

28642839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32521319-C-T

http://identifiers.org/hco/2/GRCh38#28642863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32521344-C-A

http://identifiers.org/hco/2/GRCh38#28642897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#32521378-C-A

28642897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32521378-C-T