64704126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 76580032-T-C

64704248-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, undefined
orthologous variants: 76580165-T-A

64704248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, undefined
orthologous variants: 76580165-T-C

64704304-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, undefined
orthologous variants: 76580214-C-G

64704304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, undefined
orthologous variants: 76580214-C-T

64704347-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, undefined
orthologous variants: 76580256-T-A

64704347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, undefined
orthologous variants: 76580256-T-C

http://identifiers.org/hco/14/GRCh38#64704378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#76580287-C-A

64704378-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, undefined
orthologous variants: 76580287-C-G

64704378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, undefined
orthologous variants: 76580287-C-T

http://identifiers.org/hco/14/GRCh38#64704380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#76580289-C-A

64704380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, undefined
orthologous variants: 76580289-C-T

64704460-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 76580343-T-A

64704460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 76580343-T-C

64704588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 76580476-G-A

64704588-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 76580476-G-C

64704629-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 76580517-G-C

64704629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 76580517-G-T

http://identifiers.org/hco/14/GRCh38#64704661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#76580549-C-A

64704661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 76580549-C-T

http://identifiers.org/hco/14/GRCh38#64704725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76580613-C-A

64705039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76580869-G-A

64705323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76581158-C-T

64705424-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76581256-G-C

64705533-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76581355-C-G

64705626-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76581445-G-C

64706000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76581759-C-T

64706647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76582245-T-C

64706774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76582377-G-T

64706838-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76582439-C-G

64707245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76582795-C-T

64707298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76582831-G-A

64707470-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76582963-C-G

64707544-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76583059-T-A

64707868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76583339-T-C

http://identifiers.org/hco/14/GRCh38#64707934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76583414-C-A

64707934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76583414-C-T

64707938-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76583418-T-A

64708078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76583555-G-A

64708301-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76583767-C-G

64708332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76583797-A-G

64708707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76584371-A-G

64708928-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76584813-T-A

64709281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76585317-T-C

64709366-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76585388-A-T

64709395-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76585416-G-C

64709501-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76585516-C-G

64709614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76585619-G-A

64709731-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76587051-G-C

64709751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76587071-G-T

64709816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76587166-C-T

64710713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76587840-A-G

64710799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76587927-C-T

64710956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76588066-G-A

64711028-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76588138-T-G

64714293-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76592085-G-C

64714354-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76592119-T-A

64714654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76592458-C-T

http://identifiers.org/hco/14/GRCh38#64714741-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76592559-C-A

64714955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76592770-T-C

64715042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76592858-T-C

64715298-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76593118-G-C

64715322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76593152-G-A

64715378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76593210-G-A

64715420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76593267-A-G

64715609-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76593461-T-A

64715609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76593461-T-C

http://identifiers.org/hco/14/GRCh38#64715816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76593665-C-A

64715816-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 76593665-C-G

64715816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 76593665-C-T

http://identifiers.org/hco/14/GRCh38#64715837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76593686-C-A

64715846-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 76593695-C-G

64715846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 76593695-C-T

64715864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 76593713-G-T

64715891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 76593740-G-A

64715891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 76593740-G-T

64716063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 76593931-G-A

64716063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 76593931-G-T

64716114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76593981-G-T

http://identifiers.org/hco/14/GRCh38#64716194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76594045-C-A

64716194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76594045-C-T

http://identifiers.org/hco/14/GRCh38#64716200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76594051-C-A

64716200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76594051-C-T

64716218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76594069-T-C

64716403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76594257-G-A

64716635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76594398-G-A

64716730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, undefined
orthologous variants: 76594486-G-T

64717034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76594813-G-T

64717121-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, undefined
orthologous variants: 76594868-G-C

64717214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76594954-A-G

64717222-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76594967-G-C

64717404-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76595144-T-G

64717600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76595580-C-T

64717664-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76595642-C-G

64717680-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76595658-G-T

64717722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76595702-C-T

64718251-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76596219-T-A

64718387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76596350-A-G

64718650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76596786-A-G

64719192-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76597559-G-C

64719275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76597786-C-T

64719365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76597948-G-A

64719397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76597975-A-G

64719456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76598020-T-C

64719456-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76598020-T-G

64719561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76598090-A-G

64719623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76598143-A-G

64719808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76598313-G-A

64719818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76598323-A-G

64720031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76599083-G-A

64720592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, undefined
orthologous variants: 76599561-G-A

64720613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, undefined
orthologous variants: 76599582-A-G

64720786-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76599838-C-G

64720967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76600107-G-A

64720967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76600107-G-T

64721012-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76600139-G-C

64721083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76600250-C-T

64721532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76600818-A-G

64721886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76601165-C-T

64722032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76601289-A-G

64722048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76601305-T-C

64722109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76601364-G-A

64722109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76601364-G-T

64722161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76601388-C-T

64722754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76601664-C-T

http://identifiers.org/hco/14/GRCh38#64722758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76601665-C-A

64722828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76601726-T-C

64722979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76601875-G-A

64723196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76602107-A-G

64724273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76602782-G-A

64724273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76602782-G-T

64724285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76602791-C-T

64724343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76602854-C-T

64724421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76602911-G-A

64724421-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76602911-G-C

64724421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76602911-G-T

64724648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76603092-C-T

64724791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76603220-G-A

64724791-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76603220-G-C

64724912-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76603307-T-G

64724958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76603349-G-A

64725038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76603415-T-C

64725250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76603606-G-A

64725315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76603672-C-T

64725368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76603728-C-T

64725425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76603785-A-G

64726176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76604699-C-T

64726190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76604713-G-A

64726268-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76604796-A-T

64726332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76604928-C-T

64726668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76605192-C-T

64726857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76605382-C-T

64726880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76605404-C-T

64726959-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76605470-A-T

64727421-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76606730-T-G

http://identifiers.org/hco/14/GRCh38#64727519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76606828-C-A

64727519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron variant
orthologous variants: 76606828-C-T

http://identifiers.org/hco/14/GRCh38#64727613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76606923-C-A

64727613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 76606923-C-T

64727727-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: missense variant
orthologous variants: 76607037-T-A

64727727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: synonymous variant
orthologous variants: 76607037-T-C

64727746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: missense variant
orthologous variants: 76607056-C-T

64727805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: synonymous variant
orthologous variants: 76607115-G-A

http://identifiers.org/hco/14/GRCh38#64727868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76607178-C-A

64727868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: synonymous variant
orthologous variants: 76607178-C-T

64728004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76607355-G-A

64728004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76607355-G-T

64728027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76607377-G-T

http://identifiers.org/hco/14/GRCh38#64728031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76607381-C-A

64728031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76607381-C-T

64728877-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76608864-T-A

64728888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76608879-A-G

64728891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76608882-G-T

64728897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76608888-G-T

64728910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76608902-A-G

64729075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76609059-A-G

64729160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76609118-A-G

64729160-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76609118-A-T

64729182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76609138-T-C

64729182-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76609138-T-G

64729199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76609154-G-A

64729199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76609154-G-T

http://identifiers.org/hco/14/GRCh38#64729214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76609161-C-A

64729229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76609176-A-G

64729401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76609304-G-T

64729500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76609822-G-A

64729652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76609952-C-T

64729713-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76610006-C-G

64729907-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76610214-T-A

64729990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76610304-G-A

64729991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76610305-G-A

64730009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76610324-C-T

64730175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76610472-G-A

64730182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76610479-G-A

64730182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76610479-G-T

64730566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76610784-G-A

http://identifiers.org/hco/14/GRCh38#64730580-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76610799-A-C

64730580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76610799-A-G

64730580-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76610799-A-T

64730607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76610824-T-C

64730716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76610947-A-G

64730729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76610960-G-A

http://identifiers.org/hco/14/GRCh38#64730844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76611076-C-A

64730854-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76611086-C-G

64730854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76611086-C-T

64730928-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 76611160-C-G

64730943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 76611175-G-T

http://identifiers.org/hco/14/GRCh38#64730963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76611196-C-A

http://identifiers.org/hco/14/GRCh38#64730992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76611231-C-A

64731019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76611258-G-A

64731298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76611510-G-T

64731342-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76611555-T-A

64731342-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76611555-T-G

64731596-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76611808-T-G

http://identifiers.org/hco/14/GRCh38#64731602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76611814-C-A

64731665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76611889-C-T

http://identifiers.org/hco/14/GRCh38#64732080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76612251-C-A

64732080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76612251-C-T

64732279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76612438-C-T

64732468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 76612598-T-C

http://identifiers.org/hco/14/GRCh38#64732518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76612648-C-A

64732518-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76612648-C-G

64732676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76612815-G-A

http://identifiers.org/hco/14/GRCh38#64732689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76612830-C-A

64732689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76612830-C-T

64732706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76612851-G-T

64732720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76612872-G-A

64732720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76612872-G-T

http://identifiers.org/hco/14/GRCh38#64732722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76612874-C-A

http://identifiers.org/hco/14/GRCh38#64732760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76612899-C-A

64732760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76612899-C-T

64732876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 76613015-T-C

64732913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76613052-G-A

64732913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76613052-G-T

http://identifiers.org/hco/14/GRCh38#64732972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76613111-C-A

64732972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76613111-C-T

64732991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76613125-T-C

64733027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76613160-G-A

64733027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76613160-G-T

64733044-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76613177-T-A

64733044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76613177-T-C

64733052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76613185-A-G

64733084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76613218-G-A

64733504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76613283-G-A

64733517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76613296-C-T

http://identifiers.org/hco/14/GRCh38#64733546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76613331-C-A

http://identifiers.org/hco/14/GRCh38#64733608-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76613375-A-C

64733830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76613601-T-C

http://identifiers.org/hco/14/GRCh38#64733932-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76613705-A-C

64733970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76613738-G-A

64734231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76613972-G-T

64734266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76614007-C-T

64734570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76615092-G-A

http://identifiers.org/hco/14/GRCh38#64734572-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76615094-A-C

64735094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76615317-G-A

64736521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76618089-G-A

64736592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76618168-C-T

64736688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76618217-C-T

64736694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76618223-C-T

http://identifiers.org/hco/14/GRCh38#64736823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76618351-C-A

64736823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76618351-C-T

64736906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76618431-T-C

64737049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76618547-C-T

64737060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76618557-G-A

64737060-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76618557-G-C

64737060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76618557-G-T

64737078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76618571-T-C

http://identifiers.org/hco/14/GRCh38#64737082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76618575-C-A

64737082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76618575-C-T

64737087-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76618580-T-A

64737087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76618580-T-C

64737089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76618582-C-T

http://identifiers.org/hco/14/GRCh38#64737099-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76618592-A-C

64737168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76618647-G-T

http://identifiers.org/hco/14/GRCh38#64737182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76618661-C-A

64737182-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76618661-C-G

64737207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76618683-G-A

64737207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76618683-G-T

64737212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76618688-G-T

64737312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76618781-G-A

64737312-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76618781-G-C

http://identifiers.org/hco/14/GRCh38#64737322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76618792-C-A

64737322-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76618792-C-G

64737322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76618792-C-T

64737325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76618795-G-A

http://identifiers.org/hco/14/GRCh38#64737365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76618833-C-A

64737365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76618833-C-T

64737399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76618855-A-G

64737409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76618864-A-G

64737564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76618916-C-T

64737669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76618999-G-A

64737669-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76618999-G-C

64737772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76619086-T-C

http://identifiers.org/hco/14/GRCh38#64737787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76619096-C-A

64737787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76619096-C-T

64737798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76619107-G-A

64737798-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76619107-G-C

64737798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76619107-G-T

http://identifiers.org/hco/14/GRCh38#64737824-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76619127-A-C

64737824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76619127-A-G

64737833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76619136-G-A

64737915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 76619222-G-A

64737915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 76619222-G-T

64737931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 76619238-G-T

64737960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 76619267-G-A

64737960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 76619267-G-T

http://identifiers.org/hco/14/GRCh38#64738018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76619316-C-A

64738018-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 76619316-C-G

64738018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 76619316-C-T

64738020-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 76619318-G-C

64738048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 76619346-G-A

64738048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 76619346-G-T

64738062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 76619360-G-A

64738062-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 76619360-G-C

64738062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 76619360-G-T

64738131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 76619426-G-A

64738131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 76619426-G-T

64738264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76619559-C-T

64738303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76619597-G-T

http://identifiers.org/hco/14/GRCh38#64738317-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76619610-A-C

64738317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76619610-A-G

64738405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76619686-G-A

64738449-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76619730-G-T

64738517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76619799-A-G

http://identifiers.org/hco/14/GRCh38#64738553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76619830-C-A

64738566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76619843-G-A

64738632-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76619907-C-G

64738632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76619907-C-T

64738633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76619908-T-C

http://identifiers.org/hco/14/GRCh38#64738649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76619933-C-A

64738697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76619986-G-A

64738697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76619986-G-T

64738707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76619996-G-A

64738707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76619996-G-T

64738724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76620002-T-C

64738797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76620076-G-A

64738797-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76620076-G-C

64738797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76620076-G-T

64738813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 76620092-T-C

64738841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76620120-T-C

64738873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76620152-G-T

http://identifiers.org/hco/14/GRCh38#64738903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76620182-C-A

64738903-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76620182-C-G

64738903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76620182-C-T

http://identifiers.org/hco/14/GRCh38#64738950-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76620229-A-C

http://identifiers.org/hco/14/GRCh38#64738998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76620273-C-A

64739003-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76620278-T-G

64739147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76620369-C-T

64739215-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76620435-T-A

64739257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76620469-A-G

http://identifiers.org/hco/14/GRCh38#64739515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76620611-C-A

64739598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76620690-C-T

64739647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76620738-A-G

64739816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76620889-G-T

64740070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76621532-A-G

http://identifiers.org/hco/14/GRCh38#64740097-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76621550-A-C

64740323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76621750-C-T

64740362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76621788-G-A

64740373-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76621799-G-C

64740593-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76622216-C-G

64740685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76622270-G-A

64740852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76622427-G-A

http://identifiers.org/hco/14/GRCh38#64740922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76622519-C-A

64740922-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76622519-C-G

64740922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76622519-C-T

64740997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76622595-G-A

64741011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76622610-G-A

64741029-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 76622624-G-C

64741092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 76622687-G-A

64741092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 76622687-G-T

64741200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 76622795-G-T

64741287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 76622885-T-C

64741341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 76622939-A-G

64741341-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 76622939-A-T

http://identifiers.org/hco/14/GRCh38#64741544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76623142-C-A

http://identifiers.org/hco/14/GRCh38#64741641-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76623245-A-C

64741707-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76623311-T-A

64741707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 76623311-T-C

64741711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76623315-G-T

http://identifiers.org/hco/14/GRCh38#64741749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/12/GRCm39#76623353-C-A

64741749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 76623353-C-T

64741866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 76623470-G-A

64741866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 76623470-G-T

64741942-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76623543-C-G

64741942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76623543-C-T

64742211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 76623812-G-A

64742211-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76623812-G-C

64742316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 76623917-C-T

64742403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 76623998-C-T

64742605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76624179-C-T

64742629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76624191-G-A

64742855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76624335-C-T

http://identifiers.org/hco/14/GRCh38#64742866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76624348-C-A

64742866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76624348-C-T

64742871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76624353-A-G

http://identifiers.org/hco/14/GRCh38#64742911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76624374-C-A

http://identifiers.org/hco/14/GRCh38#64742932-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76624395-A-C

http://identifiers.org/hco/14/GRCh38#64742949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76624414-C-A

64742964-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76624429-C-G

64742997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76624464-T-C

64743065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76624532-G-A

64743145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 76624612-C-T

64743217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 76624690-C-T

64743293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 76624766-G-T

64743295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 76624768-G-A

64743295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76624768-G-T

64743301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76624774-G-A

64743301-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76624774-G-C

64743340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 76624813-C-T

64743376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76624849-G-T

64743378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76624851-C-T

http://identifiers.org/hco/14/GRCh38#64743387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76624866-C-A

64743387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76624866-C-T

64743428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76624907-A-G

64743465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76624944-A-G

64743512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76624991-G-T

64743513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76624992-C-T

64743639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76625118-C-T

64743715-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76625192-G-T

64743717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76625194-G-A

64743717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76625194-G-T

64743739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76625215-G-A

64743740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76625216-G-A

64743740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76625216-G-T

64743889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76625365-G-A

64743967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76625443-G-T

64744016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76625486-G-A

64744016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76625486-G-T

64744051-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76625512-T-A

64744052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76625513-G-T

64744088-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 76625549-T-A

64744088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 76625549-T-C

http://identifiers.org/hco/14/GRCh38#64744103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76625564-C-A

http://identifiers.org/hco/14/GRCh38#64744188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76625654-C-A

64744188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 76625654-C-T

64744189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 76625655-G-A

64744189-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 76625655-G-C

64744189-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 76625655-G-T

64744191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 76625657-G-A

64744191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 76625657-G-T

64744194-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 76625660-T-A

64744196-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 76625662-T-A

64744196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 76625662-T-C

64744196-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 76625662-T-G

64744277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 76625748-G-A

64744308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 76625779-A-G

64744427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76625844-A-G

64744456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76625863-T-C

64744530-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76625931-T-A

64744530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76625931-T-C

64744533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76625934-T-C

64744535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76625936-C-T

http://identifiers.org/hco/14/GRCh38#64744545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76625946-C-A

64744545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76625946-C-T

64744589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76625990-C-T

64744591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76625992-G-A

64744591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76625992-G-T

64744667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76626061-G-A

64744667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76626061-G-T

64744670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76626064-G-T

64744673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76626067-G-A

64744673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76626067-G-T

64745209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76626276-G-T

64745226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76626291-T-C

64745326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76626367-G-T

64745327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76626368-G-A

64745327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76626368-G-T

http://identifiers.org/hco/14/GRCh38#64745397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76626439-C-A

64745397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76626439-C-T

64745404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76626443-T-C

64745485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76626507-G-T

64745531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76626543-G-A

64745531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76626543-G-T

64745555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76626567-G-T

64745589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76626594-C-T

http://identifiers.org/hco/14/GRCh38#64745733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76626729-C-A

64745733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76626729-C-T

64745806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76626832-T-C

64745842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76626869-G-T

http://identifiers.org/hco/14/GRCh38#64745918-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76626944-C-A

http://identifiers.org/hco/14/GRCh38#64746019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76627014-C-A

64746019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76627014-C-T

64746042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76627037-G-A

64746051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76627046-T-C

64746119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76627102-G-T

64746157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76627140-T-C

64746218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76627200-G-A

64746263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76627245-A-G

64746263-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76627245-A-T

64746273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76627252-G-T

64746401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76627380-T-C

http://identifiers.org/hco/14/GRCh38#64746485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76627461-C-A

64746485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76627461-C-T

64746488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76627464-T-C

64746501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76627476-G-A

64746501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76627476-G-T

64746586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76627557-C-T

http://identifiers.org/hco/14/GRCh38#64746740-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76627701-A-C

64746754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76627712-G-A

64746829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76627784-A-G

64746960-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76627908-C-G

64746960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76627908-C-T

64746998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76627931-G-A

64747051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76627987-A-G

64747068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76628004-G-A

http://identifiers.org/hco/14/GRCh38#64747127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76628053-C-A

64747170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76628092-T-C

http://identifiers.org/hco/14/GRCh38#64747195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76628117-C-A

64747195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76628117-C-T

64747219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76628140-T-C

64747265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76628185-G-T

64747290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76628208-G-A

64747323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76628242-A-G

64747357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76628275-C-T

64747460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76628393-G-A

64747460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76628393-G-T

64747489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76628413-G-A

64747650-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76628568-T-A

64747793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76628662-G-A

64747793-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76628662-G-C

64747793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76628662-G-T

64748014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76628847-T-C

http://identifiers.org/hco/14/GRCh38#64748096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76628918-C-A

64748133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76628952-G-T

64748273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76629071-G-T

64748314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76629110-T-C

64748504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76629289-A-G

64748567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76629332-C-T

64748592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76629358-G-A

http://identifiers.org/hco/14/GRCh38#64748690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76629439-C-A

64748690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76629439-C-T

64748710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76629459-G-A

64748710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76629459-G-T

64748777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76629507-G-A

64748835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76629558-T-C

64748849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76629572-G-A

64748849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: 76629572-G-T

http://identifiers.org/hco/14/GRCh38#64748924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76629646-C-A

64748999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 76629664-T-C

64748999-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 76629664-T-G

64749020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 76629685-T-C

64749115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 76629758-G-A

64749115-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 76629758-G-C

64749115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 76629758-G-T

64749228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 76629879-G-A

64749228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 76629879-G-T

64749277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 76629946-G-A

64749277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 76629946-G-T

64749360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 76630053-G-A

64749360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76630053-G-T

64749477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 76630170-C-T

64749497-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76630188-G-C

64749497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76630188-G-T

64749512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76630203-C-T

64749573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76630259-G-T

http://identifiers.org/hco/14/GRCh38#64749602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76630284-C-A

64749602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76630284-C-T

64749617-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76630299-T-A

64749906-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76630437-C-G

64749906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76630437-C-T

64749968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76630518-A-G

64750127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 76630680-G-A

64750127-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 76630680-G-C

http://identifiers.org/hco/14/GRCh38#64750188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20364
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76630742-C-A