http://identifiers.org/hco/5/GRCh38#149551648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#61688115-C-A

149551648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 61688115-C-T

149551679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 61688085-C-T

149551688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 61688076-T-C

149551845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 61687917-A-G

149551873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 61687889-T-C

149551883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 61687879-C-T

149551907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 61687859-A-G

http://identifiers.org/hco/5/GRCh38#149551914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61687852-C-A

149552392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61687445-C-T

149561383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61684365-C-T

149561451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61684262-T-C

149561467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61684246-G-A

149561468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61684245-T-C

149561548-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61684163-A-T

149561897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61683837-C-T

149562094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61683647-G-A

149562102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61683639-A-G

149562220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61683544-T-C

http://identifiers.org/hco/5/GRCh38#149562257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61683510-C-A

149562257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61683510-C-T

149562292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61683476-G-A

149562518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61683214-G-A

149562518-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61683214-G-C

149563549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61683020-A-G

149563918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61682648-T-C

149564257-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61682400-G-C

149565135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61681888-G-A

149565138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, undefined
orthologous variants: 61681885-A-G

149565139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, undefined
orthologous variants: 61681884-A-G

149565275-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61681761-G-C

149565317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61681720-A-G

149565560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61681530-T-C

http://identifiers.org/hco/5/GRCh38#149578157-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61672416-A-C

149578157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61672416-A-G

http://identifiers.org/hco/5/GRCh38#149578333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61672238-C-A

149578423-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61672144-G-C

149578740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61671006-G-A

149578740-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61671006-G-C

149581212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, undefined
orthologous variants: 61669802-G-A

149581532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61669579-A-G

149581540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 61669571-G-A

http://identifiers.org/hco/5/GRCh38#149581634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#61669522-C-A

http://identifiers.org/hco/5/GRCh38#149581668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61669498-C-A

149581668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61669498-C-T

http://identifiers.org/hco/5/GRCh38#149581758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#61669393-C-A

149581758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, undefined
orthologous variants: 61669393-C-T

149581843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, undefined
orthologous variants: 61669322-G-A

149581856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61669311-G-A

149582439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61668812-G-A

http://identifiers.org/hco/5/GRCh38#149582440-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61668811-A-C

149582440-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61668811-A-T

149583170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: -G-A

149583170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: -G-T

149584249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61667465-C-T

149584252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61667462-A-G

149587829-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61663034-C-G

149587861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61663002-T-C

149588629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61662959-A-G

149596725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61659655-G-A

149596742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61659641-G-A

149596746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61659637-G-T

149596794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61659600-G-A

149596851-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61659573-C-G

149597002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61659447-T-C

http://identifiers.org/hco/5/GRCh38#149597720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61657111-C-A

149597720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61657111-C-T

149597722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61657109-T-C

149597848-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, missense_variant
orthologous variants: 61656983-T-A

149597848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, missense_variant
orthologous variants: 61656983-T-C

149597905-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, missense_variant
orthologous variants: 61656926-T-A

149597940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 61656891-G-A

149597940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, missense_variant
orthologous variants: 61656891-G-T

149597970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61656865-T-C

149600945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61655929-C-T

149601007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61655858-G-A

149601019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61655840-G-A

149601019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61655840-G-T

149601026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61655833-T-C

149601092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61655784-T-C

149601219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 61655657-G-A

http://identifiers.org/hco/5/GRCh38#149601272-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61655597-A-C

149601272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61655597-A-G

149601272-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61655597-A-T

149601332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61655535-A-G

149601408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61655481-G-T

149609538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61651221-T-C

http://identifiers.org/hco/5/GRCh38#149609541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61651218-C-A

149609637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 61651122-A-G

149609682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 61651077-G-A

149609776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61651018-T-C

149609776-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61651018-T-G

http://identifiers.org/hco/5/GRCh38#149609810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61650983-C-A

149609810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61650983-C-T

149609817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61650975-T-C

149609818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61650974-G-A

149609818-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61650974-G-C

149609818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61650974-G-T

149609900-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61650907-T-A

http://identifiers.org/hco/5/GRCh38#149611617-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61647382-A-C

149611668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61647332-C-T

149611677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61647323-C-T

149612021-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61647017-C-G

149612021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61647017-C-T

149612543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61645277-G-A

149612898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61644837-T-C

149613177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61644610-A-G

149614263-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61643722-A-T

149614601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61643394-C-T

149614626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61643371-G-A

149614924-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61643126-G-T

149615025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61643036-G-A

149615483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61642748-T-C

149615553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61642687-A-G

149615584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61642668-C-T

149616050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61642364-G-A

149616067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61642349-G-A

149616094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61642322-G-A

149616105-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61642311-T-A

149616119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61642297-G-A

http://identifiers.org/hco/5/GRCh38#149616132-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61642284-A-C

149616499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61641977-T-C

http://identifiers.org/hco/5/GRCh38#149616501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61641975-C-A

149616501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61641975-C-T

http://identifiers.org/hco/5/GRCh38#149616510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61641964-C-A

149616510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61641964-C-T

149616613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 61641861-C-T

149616648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 61641826-G-A

149616727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 61641747-A-G

http://identifiers.org/hco/5/GRCh38#149616808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61641670-C-A

149616808-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61641670-C-G

149616808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61641670-C-T

149616849-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61641631-T-A

149616849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61641631-T-C

149616849-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61641631-T-G

149617941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, undefined
orthologous variants: 61640629-A-G

http://identifiers.org/hco/5/GRCh38#149618024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61640545-C-A

149618024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61640545-C-T

149618028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61640539-A-G

149618028-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61640539-A-T

149618055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61640508-T-C

http://identifiers.org/hco/5/GRCh38#149618123-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#61640452-A-C

149618123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, undefined
orthologous variants: 61640452-A-G

149618123-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, undefined
orthologous variants: 61640452-A-T

149618295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: synonymous_variant, undefined
orthologous variants: 61640278-C-T

149618315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61640258-G-A

149618355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61640236-C-T

149618439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61640186-A-G

149618598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61640070-G-A

149618779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61639876-A-G

http://identifiers.org/hco/5/GRCh38#149618914-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#61639615-A-C

149618914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, undefined
orthologous variants: 61639615-A-G

149618916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, undefined
orthologous variants: 61639613-C-T

149618929-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, undefined
orthologous variants: 61639600-T-A

149619133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61639435-G-A

149619133-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61639435-G-C

149619133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61639435-G-T

149619197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61639386-C-T

149619228-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61639355-G-C

http://identifiers.org/hco/5/GRCh38#149620102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61639090-C-A

149620210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61638992-G-T

149620260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61638946-T-C

http://identifiers.org/hco/5/GRCh38#149620297-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61638908-A-C

149620297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61638908-A-G

149620297-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61638908-A-T

http://identifiers.org/hco/5/GRCh38#149620310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61638895-C-A

149620347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 61638858-G-A

149620429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, missense_variant
orthologous variants: 61638776-G-A

149620450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, missense_variant
orthologous variants: 61638755-G-A

149620450-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, missense_variant
orthologous variants: 61638755-G-T

149620486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61638721-T-C

149620503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61638704-A-G

149621596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61637784-G-T

149621665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61637721-G-A

149621675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61637712-A-G

149621675-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61637712-A-T

http://identifiers.org/hco/5/GRCh38#149621682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61637705-C-A

149621682-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61637705-C-G

149621682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61637705-C-T

http://identifiers.org/hco/5/GRCh38#149621714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61637672-C-A

149621714-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61637672-C-G

149621714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61637672-C-T

http://identifiers.org/hco/5/GRCh38#149621718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61637668-C-A

149621718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61637668-C-T

149621780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: synonymous variant
orthologous variants: 61637606-C-T

149621847-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: missense variant
orthologous variants: 61637539-G-C

149621862-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: missense variant
orthologous variants: 61637524-C-G

http://identifiers.org/hco/5/GRCh38#149621882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61637504-C-A

149621883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: missense variant
orthologous variants: 61637503-T-C

149621962-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: missense variant
orthologous variants: 61637424-T-G

149621994-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: missense variant
orthologous variants: 61637392-A-T

149622370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61637049-T-C

http://identifiers.org/hco/5/GRCh38#149622538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61636896-C-A

149622802-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61636647-C-G

149622802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61636647-C-T

149623057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61636374-C-T

149623207-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61636239-G-C

149623392-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61636033-G-C

http://identifiers.org/hco/5/GRCh38#149623523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61635939-C-A

149623628-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61635825-G-C

149623898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61635547-G-T

149623963-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61635053-C-G

149623963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61635053-C-T

149623966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61635050-T-C

149623966-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61635050-T-G

149623984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61635029-T-C

149624001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61635014-T-C

149626156-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61633837-T-G

149626367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61633662-C-T

149626872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61633155-A-G

149626872-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron variant
orthologous variants: 61633155-A-T

149626898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61633129-G-A

149626898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61633129-G-T

149626908-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61633119-A-T

149626916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61633111-G-A

149626916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61633111-G-T

149626925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61633104-G-A

149626925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61633104-G-T

http://identifiers.org/hco/5/GRCh38#149626927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61633102-C-A

149626927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61633102-C-T

149627126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 61632919-T-C

http://identifiers.org/hco/5/GRCh38#149627163-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61632882-A-C

149627163-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 61632882-A-T

149627281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61632764-C-T

149627284-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61632761-T-G

http://identifiers.org/hco/5/GRCh38#149627321-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61632724-A-C

149627321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61632724-A-G

149627353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61632692-G-A

149627353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61632692-G-T

149627483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61632551-G-A

149627632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61632433-C-T

http://identifiers.org/hco/5/GRCh38#149627652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61632413-C-A

149627652-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61632413-C-G

149627701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61632370-T-C

149627814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61632265-G-A

149628228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61631805-G-A

149628262-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61631772-G-T

149628320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61631745-C-T

149628413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61631669-G-A

149628588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61631549-G-A

149629020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61631118-G-A

149629020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61631118-G-T

149629056-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61631082-T-A

149629056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61631082-T-C

149629129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61631021-G-T

149629281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61630907-A-G

149629424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61630762-G-A

149629589-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61630622-C-G

149629589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61630622-C-T

149629682-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61630517-G-C

149629698-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61630501-T-A

149629720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61630486-G-A

149629728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61630477-G-A

149629989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61629773-C-T

149630028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61629730-G-A

149630035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61629723-G-A

149630035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61629723-G-T

149630182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61629580-G-A

149630400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61629259-A-G

149630635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61629071-G-A

149631025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61628761-C-T

149631032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61628755-C-T

149631056-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61628729-G-C

149631077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61628708-A-G

149631846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61628255-G-T

149631877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61628226-G-T

149632069-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: missense variant
orthologous variants: 61628031-G-C

http://identifiers.org/hco/5/GRCh38#149632218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61627882-C-A

149632218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: 3 prime UTR variant
orthologous variants: 61627882-C-T

http://identifiers.org/hco/5/GRCh38#149632501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61627657-C-A

149632501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: 3 prime UTR variant
orthologous variants: 61627657-C-T

149632526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 61627632-G-A

149632526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 61627632-G-T

149632814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: 3 prime UTR variant
orthologous variants: 61627390-A-G

149632829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 61627375-T-C

149632830-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 61627374-G-C

149632849-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: 3 prime UTR variant
orthologous variants: 61627357-T-A

149632854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: 3 prime UTR variant
orthologous variants: 61627352-G-A

149632854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: 3 prime UTR variant
orthologous variants: 61627352-G-T

149632929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: 3 prime UTR variant
orthologous variants: 61627281-C-T

149633003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: 3 prime UTR variant
orthologous variants: 61627204-A-G

149633026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: 3 prime UTR variant
orthologous variants: 61627179-A-G

149633038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: 3 prime UTR variant
orthologous variants: 61627167-G-T

149633045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: 3 prime UTR variant
orthologous variants: 61627160-T-C

149633151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: 3 prime UTR variant
orthologous variants: 61627060-G-T

149633286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: 3 prime UTR variant
orthologous variants: 61626929-A-G

149633581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: 3 prime UTR variant
orthologous variants: 61626073-G-A

149633581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: 3 prime UTR variant
orthologous variants: 61626073-G-T

http://identifiers.org/hco/5/GRCh38#149633644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61626008-C-A

149633644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: 3 prime UTR variant
orthologous variants: 61626008-C-T

149633818-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: 3 prime UTR variant
orthologous variants: 61625833-T-G

149633931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: 3 prime UTR variant
orthologous variants: 61625727-T-C

149633968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: 3 prime UTR variant
orthologous variants: 61625690-T-C

http://identifiers.org/hco/5/GRCh38#149634010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61625650-C-A

149634162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: 3 prime UTR variant
orthologous variants: 61625503-G-T

149634323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: 3 prime UTR variant
orthologous variants: 61625349-G-T

http://identifiers.org/hco/5/GRCh38#149634349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61625323-C-A

149634349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: 3 prime UTR variant
orthologous variants: 61625323-C-T

149634361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: 3 prime UTR variant
orthologous variants: 61625311-G-T

149634589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: 3 prime UTR variant
orthologous variants: 61625086-G-T

149634708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: 3 prime UTR variant
orthologous variants: 61624969-T-C

http://identifiers.org/hco/5/GRCh38#149634747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61624931-C-A

149634747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: 3 prime UTR variant
orthologous variants: 61624931-C-T

149634761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: 3 prime UTR variant
orthologous variants: 61624917-G-A

149634792-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: 3 prime UTR variant
orthologous variants: 61624885-C-G

http://identifiers.org/hco/5/GRCh38#149634836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61624841-C-A

149634836-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: 3 prime UTR variant
orthologous variants: 61624841-C-G

http://identifiers.org/hco/5/GRCh38#149634838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61624839-C-A

149634838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: 3 prime UTR variant
orthologous variants: 61624839-C-T

149634956-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34430
most severe consequence: 3 prime UTR variant
orthologous variants: 61624738-T-A