http://identifiers.org/hco/1/GRCh38#34166941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127879944-C-A

34166941-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: 5 prime UTR variant
orthologous variants: 127879944-C-G

http://identifiers.org/hco/1/GRCh38#34167123-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127879755-A-C

34167123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: 5 prime UTR variant
orthologous variants: 127879755-A-G

34167123-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: 5 prime UTR variant
orthologous variants: 127879755-A-T

34167252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127879639-C-T

http://identifiers.org/hco/1/GRCh38#34167292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127879598-C-A

34167292-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127879598-C-G

34167292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127879598-C-T

34167303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127879587-G-T

34167537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127879405-A-G

34167594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron_variant, undefined
orthologous variants: 127879354-C-T

http://identifiers.org/hco/1/GRCh38#34167969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127878995-C-A

34167969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127878995-C-T

34168128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127878866-T-C

34168224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127878742-G-A

34168224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127878742-G-T

34168276-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127878675-T-G

34168443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127878283-T-C

34168485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127878222-G-A

34168718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127878031-T-C

34168869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127877875-G-A

34168869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127877875-G-T

34168891-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127877849-G-C

34168922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127877818-G-A

34168976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127877762-T-C

34168978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127877760-T-C

34168988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127877750-G-A

34169148-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127877444-G-T

34169422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127877145-G-T

34169432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127877135-T-C

34169625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127876941-G-A

34169625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127876941-G-T

34169745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127876494-G-A

34169754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127876483-A-G

34169773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127876471-T-C

34169859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127876414-G-A

34169956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127876318-G-A

34170439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127874959-A-G

34170814-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127874665-G-C

34170884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127874591-G-A

34170884-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127874591-G-C

34171307-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127874215-C-G

34171445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127873788-G-A

34171455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127873778-A-G

34171918-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127873284-G-C

34172017-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127873177-G-C

34172045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127873149-C-T

34172069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127873125-A-G

34172080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127873114-G-A

http://identifiers.org/hco/1/GRCh38#34172252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127872165-C-A

34172411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127872030-G-A

34172965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127871331-T-C

34173359-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127870772-C-G

34173483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127870598-T-C

34173958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127869867-G-A

34174182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127869283-A-G

http://identifiers.org/hco/1/GRCh38#34174200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127869264-C-A

34174285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127869178-A-G

34175229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127867057-G-T

34175537-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127866747-T-G

34175633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127866646-T-C

34175653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127866626-C-T

34176119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127866239-A-G

34176343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127866053-G-A

34176875-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127865560-G-C

34177059-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 127865364-C-G

34177059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 127865364-C-T

34177209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 127865208-G-A

34177237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 127865183-G-A

34177397-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 127865012-G-T

http://identifiers.org/hco/1/GRCh38#34177675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127864737-C-A

34177675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 127864737-C-T

34177900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 127864506-G-A

34178144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127864273-G-A

34178145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127864272-G-A

34178173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127864244-G-A

http://identifiers.org/hco/1/GRCh38#34178235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127864196-C-A

34178235-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127864196-C-G

34178235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127864196-C-T

34178257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127864162-A-G

34178459-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127863957-T-A

34178483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127863932-G-A

34178764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127863661-G-A

34179115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127863291-A-G

34179255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127863148-A-G

34179421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127862980-G-A

34179823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127862591-G-T

34179895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127862443-T-C

34179915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127862423-A-G

34180004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127862336-A-G

34180088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127862217-A-G

34180160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127862160-A-G

34180713-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127861565-T-G

34180832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127861446-C-T

34180930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127861167-T-C

34181030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127861095-C-T

34181189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127860952-C-T

34181264-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127860888-C-G

34181352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127860801-G-A

http://identifiers.org/hco/1/GRCh38#34181369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127860785-C-A

34181406-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127860750-T-A

34181593-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127860571-C-G

34181593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127860571-C-T

34181607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127860557-T-C

34181679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127860490-T-C

34181706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127860463-C-T

34181842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127860348-A-G

34183141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127859825-G-T

34183164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127859802-T-C

http://identifiers.org/hco/1/GRCh38#34183396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127859555-C-A

34183469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127859478-G-A

34184290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127859038-G-A

34184325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127859004-G-A

34184328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127859001-T-C

34185032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127857853-G-A

34185646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127857399-G-A

34185646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127857399-G-T

34185736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127857311-A-G

http://identifiers.org/hco/1/GRCh38#34185785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127857266-C-A

34185785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127857266-C-T

34185822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127857239-G-A

34185837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127857224-G-A

34185948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127857127-T-C

34186122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127856915-A-G

http://identifiers.org/hco/1/GRCh38#34186129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127856908-C-A

34186194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127856847-G-T

34186702-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127856240-T-A

34186765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127856197-G-A

34186839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127856129-C-T

34186862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127856105-G-T

34186963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127856004-T-C

34187065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127855871-T-C

34187212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127855734-C-T

34187234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127855712-G-T

34187381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127855581-T-C

34187512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127855468-A-G

34188044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127855016-A-G

34188088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127854979-A-G

34188099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127854971-C-T

34188109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127854961-G-T

34188186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127854905-G-A

34188186-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127854905-G-C

34188258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127854856-T-C

34188481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127854651-A-G

34188585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127854540-T-C

34188598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127854521-G-A

34188628-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127854487-C-G

34188787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127854328-C-T

34189050-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127854133-C-G

34189050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127854133-C-T

34189280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127853915-G-A

34189290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127853905-G-A

34189546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127853690-T-C

34189560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127853676-G-A

34189606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127853634-G-A

34189636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127853603-G-A

34189655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127853585-A-G

34189695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127853547-G-T

http://identifiers.org/hco/1/GRCh38#34190902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127851488-C-A

34190902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127851488-C-T

34191097-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127851267-A-T

34191159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127851205-G-A

34191316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127851102-G-T

34191512-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127850922-T-A

34191562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127850884-A-G

34191599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127850846-C-T

34191799-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127850630-A-T

34191876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127850552-T-C

34191988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127850449-G-A

34192231-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127850167-T-A

34192231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127850167-T-C

34192309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127849990-T-C

34192386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127849881-G-A

34192404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127849869-T-C

34192575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127849555-T-C

34193190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127848909-G-A

34193287-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127848815-C-G

34193375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127848726-A-G

34193437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127848664-T-C

34193569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127848532-T-C

34193700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127848400-C-T

http://identifiers.org/hco/1/GRCh38#34193721-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127848378-A-C

34193885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127848245-A-G

34193893-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127848237-G-C

34193894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127848236-A-G

34193917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127848209-G-A

34193917-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127848209-G-C

34194220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127848052-C-T

34194443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127847813-G-A

34194616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127847227-T-C

34194728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127847127-G-A

34194974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127846870-G-A

34195027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127846825-G-A

34195760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127846589-C-T

34195773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127846576-T-C

34195775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127846574-C-T

34195779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127846570-G-T

34195781-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127846568-T-G

34195783-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127846566-T-A

34195783-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127846566-T-G

34195785-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127846564-T-G

34195801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127846548-T-C

34196209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127846144-G-A

34196224-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127846129-C-G

34196314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127846038-G-A

http://identifiers.org/hco/1/GRCh38#34196472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127845940-C-A

34196620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127845786-T-C

34196719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127845681-T-C

34196738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127845663-A-G

34197165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127845471-G-A

34197165-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127845471-G-T

http://identifiers.org/hco/1/GRCh38#34197176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127845460-C-A

34197176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127845460-C-T

http://identifiers.org/hco/1/GRCh38#34197177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127845459-C-A

34197177-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127845459-C-G

34197177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127845459-C-T

34197343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 127845307-C-T

34197566-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: missense variant
orthologous variants: 127845084-G-C

34197593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: missense variant
orthologous variants: 127845057-G-A

34197593-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: missense variant
orthologous variants: 127845057-G-C

34197736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: missense variant
orthologous variants: 127844914-C-T

http://identifiers.org/hco/1/GRCh38#34197844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127844806-C-A

34197886-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: missense variant
orthologous variants: 127844764-C-G

34197886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: missense variant
orthologous variants: 127844764-C-T

34198002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127844654-G-A

34198002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127844654-G-T

34198719-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127843544-A-T

34198752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127843515-A-G

http://identifiers.org/hco/1/GRCh38#34199003-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127843275-A-C

34199055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127843224-G-T

34199121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127843160-G-A

34199256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127842976-G-A

http://identifiers.org/hco/1/GRCh38#34199371-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127842840-A-C

34199371-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127842840-A-T

http://identifiers.org/hco/1/GRCh38#34199512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127842705-C-A

34199552-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127842656-G-C

34199757-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127842007-C-G

34200210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron_variant, undefined
orthologous variants: 127841554-A-G

34200232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron_variant, undefined
orthologous variants: 127841532-T-C

34200243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron_variant, undefined
orthologous variants: 127841521-G-A

34200340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127841375-T-C

34200343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127841372-G-A

34200392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron_variant, undefined
orthologous variants: 127841315-G-A

34200591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127840860-G-A

34200591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127840860-G-T

34200740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127840731-G-A

34200778-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: missense variant
orthologous variants: 127840693-G-C

34200778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: missense variant
orthologous variants: 127840693-G-T

34201128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127840370-C-T

34201255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127840241-T-C

34201505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127839952-C-T

34201612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127839568-A-G

34201612-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127839568-A-T

34201754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127839450-G-T

34201930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127839300-T-C

34201964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127839266-G-T

34202248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: synonymous variant
orthologous variants: 127838986-T-C

34202267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 127838967-A-G

http://identifiers.org/hco/1/GRCh38#34202357-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127838920-A-C

34202357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127838920-A-G

34202381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127838895-T-C

http://identifiers.org/hco/1/GRCh38#34202401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127838879-C-A

34202451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127838837-G-A

http://identifiers.org/hco/1/GRCh38#34202456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127838832-C-A

34202487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127838802-T-C

34203684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127838620-A-G

34203785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127838519-G-T

34203814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127838490-C-T

34203820-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127838484-C-G

34203820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127838484-C-T

34203902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127838403-T-C

34204374-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127838128-C-G

34204374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127838128-C-T

34204457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127838061-G-T

34204466-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127838052-T-G

34204536-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127838012-G-C

34204553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127837995-C-T

34204968-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127837736-T-A

34206149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127836066-G-A

34206150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127836065-G-A

34206637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127835975-G-A

34206642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127835970-A-G

34206644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127835968-A-G

http://identifiers.org/hco/1/GRCh38#34206768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127835863-C-A

34206768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127835863-C-T

34207257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127835149-T-C

34207632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127834715-G-A

34208002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127834079-C-T

34208008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127834073-C-T

34208026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127834056-A-G

http://identifiers.org/hco/1/GRCh38#34208034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127834047-C-A

34208034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127834047-C-T

34208102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127833959-G-A

34208102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127833959-G-T

34208190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: missense variant
orthologous variants: 127833870-T-C

http://identifiers.org/hco/1/GRCh38#34208318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127833744-C-A

34208318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127833744-C-T

http://identifiers.org/hco/1/GRCh38#34208321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127833741-C-A

34208321-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127833741-C-G

34208376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127833682-G-A

34208376-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127833682-G-C

34208376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127833682-G-T

34208384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127833674-G-A

34208384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127833674-G-T

34208672-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127833434-C-G

34208672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127833434-C-T

34208796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127833311-A-G

34209237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127832896-A-G

http://identifiers.org/hco/1/GRCh38#34209372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127832451-C-A

34209378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127832445-T-C

34209384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127832439-C-T

34209422-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127832401-T-G

34209432-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127832391-T-G

34209499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127832327-C-T

34209621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127832203-C-T

34209782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127832063-C-T

34209873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127831991-G-A

34210450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127831475-C-T

34211048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127830863-T-C

34211125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127830800-C-T

34211180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127830754-C-T

34211402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127830601-C-T

34211449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127830555-C-T

http://identifiers.org/hco/1/GRCh38#34211964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127829952-C-A

34212000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127829918-A-G

http://identifiers.org/hco/1/GRCh38#34212108-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127829873-A-C

34212108-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127829873-A-T

34212152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127829854-G-A

http://identifiers.org/hco/1/GRCh38#34212183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127829822-C-A

34212216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: missense variant
orthologous variants: 127829788-C-T

34212334-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: missense variant
orthologous variants: 127829670-T-G

34212423-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127829572-T-A

34212546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127829444-G-A

34212546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127829444-G-T

34212552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127829438-G-A

34212552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127829438-G-T

34212603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127829389-G-T

34212752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127829232-T-C

34213247-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127828784-T-A

34213399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127828617-G-T

34214412-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127827494-T-G

34214471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127827449-C-T

http://identifiers.org/hco/1/GRCh38#34214871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127827099-C-A

34216252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127824841-G-T

34216539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127824387-G-A

34216539-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127824387-G-T

34216760-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127824163-T-G

34216819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127824066-C-T

34216867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127824006-T-C

34217253-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127823728-G-C

34217583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127822999-T-C

34217749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127822816-C-T

34217807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127822757-T-C

34217873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127822691-T-C

34218072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127822491-G-A

34218262-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127822286-T-G

34218442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127822114-G-A

http://identifiers.org/hco/1/GRCh38#34218565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127821990-C-A

34218618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127821937-A-G

34218654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127821901-T-C

http://identifiers.org/hco/1/GRCh38#34218670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127821885-C-A

34218670-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: intron variant
orthologous variants: 127821885-C-G

34218714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: missense variant
orthologous variants: 127821841-A-G

34218927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: 3 prime UTR variant
orthologous variants: 127821562-A-G

34218930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: 3 prime UTR variant
orthologous variants: 127821559-T-C

34218930-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: 3 prime UTR variant
orthologous variants: 127821559-T-G

34218932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: 3 prime UTR variant
orthologous variants: 127821557-G-A

34218932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: 3 prime UTR variant
orthologous variants: 127821557-G-T

http://identifiers.org/hco/1/GRCh38#34218940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127821549-C-A

34218940-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: 3 prime UTR variant
orthologous variants: 127821549-C-G

34218946-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: 3 prime UTR variant
orthologous variants: 127821543-T-A

34218946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: 3 prime UTR variant
orthologous variants: 127821543-T-C

34218946-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28250
most severe consequence: 3 prime UTR variant
orthologous variants: 127821543-T-G