165078136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: 3 prime UTR variant
orthologous variants: 65423387-G-T

http://identifiers.org/hco/4/GRCh38#165078143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#65423380-C-A

165078143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: 3 prime UTR variant
orthologous variants: 65423380-C-T

165078150-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: 3 prime UTR variant
orthologous variants: 65423373-T-A

165078153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: 3 prime UTR variant
orthologous variants: 65423370-G-A

165078200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: 3 prime UTR variant
orthologous variants: 65423333-T-C

165078201-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: 3 prime UTR variant
orthologous variants: 65423332-A-T

http://identifiers.org/hco/4/GRCh38#165078292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#65423145-C-A

165078292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: 3 prime UTR variant
orthologous variants: 65423145-C-T

http://identifiers.org/hco/4/GRCh38#165078307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#65423130-C-A

165078307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: 3 prime UTR variant
orthologous variants: 65423130-C-T

165078378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: 3 prime UTR variant
orthologous variants: 65423046-G-A

165078473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: 3 prime UTR variant
orthologous variants: 65422942-C-T

165078620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: 3 prime UTR variant
orthologous variants: 65422399-C-T

http://identifiers.org/hco/4/GRCh38#165078681-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#65422339-A-C

165079162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: 3 prime UTR variant
orthologous variants: 65421927-C-T

165079295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: 3 prime UTR variant
orthologous variants: 65421793-T-C

165079304-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: 3 prime UTR variant
orthologous variants: 65421784-A-T

http://identifiers.org/hco/4/GRCh38#165079332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#65421756-C-A

165079332-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: 3 prime UTR variant
orthologous variants: 65421756-C-G

165079398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: 3 prime UTR variant
orthologous variants: 65421721-A-G

http://identifiers.org/hco/4/GRCh38#165079483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#65421646-C-A

165079483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: 3 prime UTR variant
orthologous variants: 65421646-C-T

http://identifiers.org/hco/4/GRCh38#165079491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#65421641-C-A

165079491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: 3 prime UTR variant
orthologous variants: 65421641-C-T

165079508-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: 3 prime UTR variant
orthologous variants: 65421624-A-T

165079510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: 3 prime UTR variant
orthologous variants: 65421622-A-G

165079510-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: 3 prime UTR variant
orthologous variants: 65421622-A-T

http://identifiers.org/hco/4/GRCh38#165079516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#65421609-C-A

165079516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: 3 prime UTR variant
orthologous variants: 65421609-C-T

165079554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: 3 prime UTR variant
orthologous variants: 65421572-G-T

http://identifiers.org/hco/4/GRCh38#165079557-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#65421569-A-C

165079557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: 3 prime UTR variant
orthologous variants: 65421569-A-G

165079570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: 3 prime UTR variant
orthologous variants: 65421555-T-C

165079573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: 3 prime UTR variant
orthologous variants: 65421552-A-G

165079573-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: 3 prime UTR variant
orthologous variants: 65421552-A-T

165079620-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: 3 prime UTR variant
orthologous variants: 65421516-T-A

165079620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: 3 prime UTR variant
orthologous variants: 65421516-T-C

165079646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: 3 prime UTR variant
orthologous variants: 65421496-A-G

165079657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: 3 prime UTR variant
orthologous variants: 65421485-C-T

165079659-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: stop lost
orthologous variants: 65421483-C-G

165079815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65421343-T-C

165079871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65421288-A-G

165085666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: synonymous variant
orthologous variants: 65418211-T-C

http://identifiers.org/hco/4/GRCh38#165085704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#65418174-C-A

165085704-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65418174-C-G

165085704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65418174-C-T

165085727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65418146-G-T

http://identifiers.org/hco/4/GRCh38#165085805-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#65418022-A-C

165085805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65418022-A-G

165085886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65417943-G-A

165088451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65416999-C-T

165088572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron_variant, missense_variant
orthologous variants: 65416878-A-G

165088575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron_variant, missense_variant
orthologous variants: 65416875-C-T

165088590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron_variant, missense_variant
orthologous variants: 65416860-A-G

165088607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 65416843-G-A

165088632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65416818-G-A

165088632-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65416818-G-T

http://identifiers.org/hco/4/GRCh38#165100513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#65412447-C-A

http://identifiers.org/hco/4/GRCh38#165100738-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#65412149-A-C

http://identifiers.org/hco/4/GRCh38#165100760-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#65412127-A-C

165100761-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 65412126-A-T

165100842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 65412045-A-G

165100896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 65411991-G-A

165100896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 65411991-G-T

165103135-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65408999-T-G

165105031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65404179-C-T

165105349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65403871-A-G

165112343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron_variant, undefined
orthologous variants: 65400314-C-T

165112632-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65400088-G-T

165112653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron_variant, undefined
orthologous variants: 65400068-G-A

165112653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron_variant, undefined
orthologous variants: 65400068-G-T

http://identifiers.org/hco/4/GRCh38#165112668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#65400053-C-A

165112773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 65399957-T-C

165112794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 65399936-A-G

http://identifiers.org/hco/4/GRCh38#165112826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#65399905-C-A

165112826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 65399905-C-T

165112905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65399828-G-A

165112905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65399828-G-T

165112916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65399818-G-A

165112916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65399818-G-T

165112921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65399813-G-A

165112921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65399813-G-T

http://identifiers.org/hco/4/GRCh38#165112952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#65399783-C-A

165112952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65399783-C-T

http://identifiers.org/hco/4/GRCh38#165112975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#65399759-C-A

165112975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65399759-C-T

165113009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65399726-C-T

165113013-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65399722-C-G

165113013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65399722-C-T

165129923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65396588-G-A

165129923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65396588-G-T

165130571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65395408-T-C

165130622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65395374-A-G

165131342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65394317-A-G

165131470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron_variant, undefined
orthologous variants: 65394243-A-G

165131475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron_variant, undefined
orthologous variants: 65394238-T-C

165131653-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65394082-T-A

165131975-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65393564-T-A

165132393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65392176-T-C

165132393-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65392176-T-G

165132405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65392164-G-A

165132452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65392118-G-A

165132624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65391452-G-A

165132631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65391445-G-A

165132663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65391414-C-T

165132666-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65391411-T-A

165141856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65387774-A-G

165141880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65387743-G-A

165141884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65387739-C-T

165142890-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65383879-G-C

165142895-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65383874-C-G

165142993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65383781-T-C

165143167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65383613-A-G

165143182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65383610-C-T

http://identifiers.org/hco/4/GRCh38#165145100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#65382323-C-A

165145142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65382270-A-G

165145216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65382126-A-G

165145255-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65381975-T-A

165145412-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65381827-A-T

http://identifiers.org/hco/4/GRCh38#165145562-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#65381707-A-C

165145772-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65381591-C-G

165146201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65380141-G-A

165151651-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65379857-T-G

165151734-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65379776-A-T

165152640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron_variant, undefined
orthologous variants: 65379316-A-G

165152640-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron_variant, undefined
orthologous variants: 65379316-A-T

165152872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron_variant, undefined
orthologous variants: 65379083-C-T

165152933-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65379021-C-G

http://identifiers.org/hco/4/GRCh38#165153246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#65378700-C-A

165153276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65378670-A-G

165154377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65375864-G-A

165160537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65371623-A-G

165160627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65371535-C-T

165161944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65369922-T-C

165162031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65369512-G-A

165168769-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65361441-A-T

165168801-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65361408-T-G

http://identifiers.org/hco/4/GRCh38#165170001-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#65360167-A-C

165170127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65360042-A-G

165170158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65360008-G-A

165170909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65357067-C-T

165170914-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65357062-C-G

165170916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65357060-G-A

165171298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65356636-T-C

165171318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65356622-T-C

165174469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65355587-T-C

165174516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65355536-T-C

165174752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65355363-C-T

165174845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65355291-G-A

165175010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65355117-G-A

http://identifiers.org/hco/4/GRCh38#165175487-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#65354784-A-C

165175525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65354750-T-C

165175722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65354575-C-T

165176111-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65354231-T-A

165176152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65354199-G-A

165176214-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65354147-A-T

165176334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65354032-C-T

165176338-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65354028-C-G

165176338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65354028-C-T

165176758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65353349-G-A

165176788-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65353322-C-G

165176788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65353322-C-T

165176821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65353292-C-T

165176955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65353142-C-T

165177558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65351876-T-C

165177922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65350180-T-C

165177976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron_variant, undefined
orthologous variants: 65350131-T-C

165177980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron_variant, undefined
orthologous variants: 65350127-A-G

165178186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65349920-A-G

165183549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65336700-T-C

165183579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65336670-T-C

165183851-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65336413-T-A

165183878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65336386-G-T

165184352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65335372-A-G

165184435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65335288-G-A

165184790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65334705-T-C

165184794-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65334701-C-G

165185458-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65333705-C-G

165185694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65333444-A-G

165185954-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65332453-T-G

165186122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65331919-T-C

165186467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65331541-A-G

165186607-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65331401-G-C

165186619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65331389-T-C

165186679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65331325-T-C

http://identifiers.org/hco/4/GRCh38#165186968-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#65331056-A-C

165187058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65330963-G-T

165189814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65329888-G-A

165190201-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65329588-G-C

165190239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65329568-C-T

165190318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65329528-A-G

165190647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65329174-G-T

165190952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65328842-A-G

165191102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65328694-A-G

165191418-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65328405-A-T

165191774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65327631-G-T

165192145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65324752-G-A

165192184-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65324709-A-T

165192475-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65324426-G-C

165193815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65322625-A-G

165196834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65315518-C-T

165196867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65315482-T-C

165197145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65315182-A-G

165197629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65314699-C-T

165197632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65314696-T-C

165197658-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65314676-C-G

165197684-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65314650-G-C

165197847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65314458-T-C

165197871-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65314438-T-G

165197902-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65314410-A-T

165198556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65312856-A-G

165198596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron_variant, undefined
orthologous variants: 65312814-T-C

165198994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65312428-T-C

165198994-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65312428-T-G

165199100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65312330-A-G

165199205-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65312246-A-T

http://identifiers.org/hco/4/GRCh38#165199349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#65311318-C-A

165199349-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65311318-C-G

165199684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65310986-T-C

165201127-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65308556-T-G

165201439-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65308269-G-C

http://identifiers.org/hco/4/GRCh38#165201535-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#65308161-A-C

165201721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65307994-A-G

165201732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65307983-G-T

http://identifiers.org/hco/4/GRCh38#165201912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#65307808-C-A

165202060-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65307709-T-A

165202128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65307644-A-G

165202365-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65307401-T-A

165202440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65307333-A-G

http://identifiers.org/hco/4/GRCh38#165202813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#65306413-C-A

165202813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65306413-C-T

165202836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65306390-T-C

165203841-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65304900-G-C

165203958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65304788-C-T

165204464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65304498-A-G

http://identifiers.org/hco/4/GRCh38#165204485-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#65304478-A-C

http://identifiers.org/hco/4/GRCh38#165206624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#65303470-C-A

165206624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65303470-C-T

http://identifiers.org/hco/4/GRCh38#165206868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#65303232-C-A

165206943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65303161-T-C

165207406-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron_variant, undefined
orthologous variants: 65302744-G-C

165207406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron_variant, undefined
orthologous variants: 65302744-G-T

165207445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron_variant, undefined
orthologous variants: 65302729-C-T

165207452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron_variant, undefined
orthologous variants: 65302722-C-T

http://identifiers.org/hco/4/GRCh38#165207583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#65302619-C-A

165207583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 65302619-C-T

165207620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 65302577-G-A

165207620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 65302577-G-T

http://identifiers.org/hco/4/GRCh38#165207635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#65302562-C-A

165207635-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 65302562-C-G

165207635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 65302562-C-T

165207698-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 65302484-G-C

165207698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 65302484-G-T

165207798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 65302387-G-A

165207798-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 65302387-G-C

165207798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 65302387-G-T

http://identifiers.org/hco/4/GRCh38#165207887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#65302298-C-A

165207887-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, synonymous_variant
orthologous variants: 65302298-C-G

165207887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, synonymous_variant
orthologous variants: 65302298-C-T

165208132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65302083-C-T

165208436-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: intron variant
orthologous variants: 65301743-T-G

165208507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26775
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 65301668-T-C