95433614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: 5 prime UTR variant
orthologous variants: 119025352-A-G

95433637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: 5 prime UTR variant
orthologous variants: 119025375-G-A

95433637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: 5 prime UTR variant
orthologous variants: 119025375-G-T

http://identifiers.org/hco/13/GRCh38#95433654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#119025392-C-A

95433654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: 5 prime UTR variant
orthologous variants: 119025392-C-T

95433686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: 5 prime UTR variant
orthologous variants: 119025424-G-T

95433707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: 5 prime UTR variant
orthologous variants: 119025442-G-A

95433707-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: 5 prime UTR variant
orthologous variants: 119025442-G-C

95433707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: 5 prime UTR variant
orthologous variants: 119025442-G-T

95433761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: 5 prime UTR variant
orthologous variants: 119025496-T-C

http://identifiers.org/hco/13/GRCh38#95433872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#119025607-C-A

95433872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: synonymous variant
orthologous variants: 119025607-C-T

95433878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: synonymous variant
orthologous variants: 119025613-G-A

95433878-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: synonymous variant
orthologous variants: 119025613-G-C

95433947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: missense variant
orthologous variants: 119025682-A-G

http://identifiers.org/hco/13/GRCh38#95434125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#119025858-C-A

95434125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119025858-C-T

95434203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119025924-T-C

95434312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119026037-G-A

95434402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119026127-T-C

95434931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119026206-A-G

95435034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119026295-G-A

95435231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119026466-C-T

95435239-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119026474-G-C

95435981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119026764-A-G

95435995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119026778-T-C

95436139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119026921-A-G

95436165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119026956-A-G

95436183-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119026974-T-A

95436546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119027327-G-A

95436565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119027346-G-A

95436594-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119027373-T-A

95441200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119028732-G-T

95442268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119029188-G-T

95442359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119029256-G-A

95443475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119029446-G-A

95443490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119029462-G-A

95443493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119029465-A-G

95443508-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119029478-C-G

95443508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119029478-C-T

95443516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119029486-C-T

95443696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119029661-T-C

95443783-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119029728-G-C

95443813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119029758-G-A

95444066-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119030021-T-A

95444417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119030686-A-G

http://identifiers.org/hco/13/GRCh38#95444577-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#119030895-A-C

95444581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119030899-C-T

95444719-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119031035-C-G

95444719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119031035-C-T

95446899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119033416-T-C

95446967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119033483-A-G

95447008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119033514-G-A

95447057-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119033563-G-C

95447057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119033563-G-T

95447182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119033700-T-C

95447212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119033732-G-A

95447409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119033864-G-A

95447710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119034105-T-C

95447722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119034117-G-A

95447802-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119034202-C-G

95447872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119034265-C-T

95447873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119034266-G-A

95447948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119034353-G-A

95447948-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119034353-G-C

95447996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119034419-C-T

95450423-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119035156-T-A

95450612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119035335-C-T

95450675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119035387-A-G

95450888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119035609-C-T

95450910-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119035633-A-T

95451178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119035841-G-A

http://identifiers.org/hco/13/GRCh38#95451315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#119035920-C-A

95452349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119037204-T-C

95454154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119038510-G-A

95454154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119038510-G-T

95454779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119038759-A-G

95454824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119038803-G-A

95455483-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119041063-A-T

95455596-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119041168-G-C

95455944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119041520-A-G

95469140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119045027-C-T

95469418-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119045326-G-T

95469521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119045429-G-T

95469532-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119045440-C-G

95469532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119045440-C-T

http://identifiers.org/hco/13/GRCh38#95469756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#119045844-C-A

95470394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119046692-C-T

95470511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119046819-G-A

95470596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119046898-G-A

95470799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119047099-G-A

95470813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119047106-T-C

95470846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119047138-G-A

http://identifiers.org/hco/13/GRCh38#95470929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#119047213-C-A

95470929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119047213-C-T

95471074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119047323-G-T

95471163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119047419-G-T

95472697-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119048079-T-A

95472697-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119048079-T-G

95473436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119048310-G-A

95473441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119048315-G-A

95473483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119048356-G-A

95473483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119048356-G-T

95473709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119048569-C-T

95476032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119051552-G-A

95476039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119051559-A-G

95476110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119051632-G-A

95476177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119051682-C-T

95476210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119051714-G-A

95476286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119051777-C-T

95476437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119051901-C-T

95476441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119051905-G-A

95476570-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119052038-G-C

95476594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119052062-G-A

95476865-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119052321-T-G

http://identifiers.org/hco/13/GRCh38#95476994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#119052423-C-A

95476994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119052423-C-T

95476997-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119052426-G-C

95477286-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119053150-G-C

95477352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119053188-C-T

http://identifiers.org/hco/13/GRCh38#95477463-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#119053306-A-C

95477501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119053347-G-T

95477686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119053480-A-G

95477705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119053499-C-T

http://identifiers.org/hco/13/GRCh38#95477950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#119053695-C-A

95477950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119053695-C-T

http://identifiers.org/hco/13/GRCh38#95478649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#119054077-C-A

95478666-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119054094-T-A

95478753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119054178-G-A

95478885-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119054284-G-C

95480378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119054719-G-A

95480438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119054790-G-A

95480526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119054852-T-C

95494242-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119057649-A-T

http://identifiers.org/hco/13/GRCh38#95494285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#119057697-C-A

95494285-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119057697-C-G

95494285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119057697-C-T

http://identifiers.org/hco/13/GRCh38#95494421-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#119057808-A-C

95494443-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119057830-C-G

95494756-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119058084-T-G

http://identifiers.org/hco/13/GRCh38#95496976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#119059242-C-A

http://identifiers.org/hco/13/GRCh38#95497032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#119059285-C-A

95497032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119059285-C-T

95497044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119059296-G-T

95497076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119059332-A-G

95497095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119059351-C-T

http://identifiers.org/hco/13/GRCh38#95497113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#119059369-C-A

95497154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119059404-G-A

95497154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119059404-G-T

http://identifiers.org/hco/13/GRCh38#95497452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#119059716-C-A

95498004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119060256-G-A

95498338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119060592-T-C

95498562-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119060997-T-G

95498595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119061032-A-G

95498597-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119061034-G-C

95498603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119061040-C-T

http://identifiers.org/hco/13/GRCh38#95498638-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#119061095-A-C

95498638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119061095-A-G

95498691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119061147-A-G

95498691-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119061147-A-T

95499085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119061516-A-G

95508214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119062123-A-G

95508340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119062249-G-A

95508503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119062405-C-T

95508504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119062406-C-T

http://identifiers.org/hco/13/GRCh38#95509655-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#119063117-A-C

95509789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119063313-G-A

95509915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119063433-G-T

95509947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119063472-T-C

95510067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119063609-C-T

95510068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119063610-G-A

95510068-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119063610-G-C

95510125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119063667-T-C

95510224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119063734-A-G

http://identifiers.org/hco/13/GRCh38#95510375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#119063879-C-A

95510758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119064320-A-G

95510992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119064600-T-C

95511121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119064727-C-T

95511272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119064866-T-C

http://identifiers.org/hco/13/GRCh38#95511346-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#119064939-A-C

95511346-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119064939-A-T

http://identifiers.org/hco/13/GRCh38#95511471-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#119064992-A-C

95513215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119067050-C-T

http://identifiers.org/hco/13/GRCh38#95513474-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#119067280-A-C

http://identifiers.org/hco/13/GRCh38#95513531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#119067339-C-A

95513573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119067383-A-G

95513605-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119067747-T-A

95528503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119069975-A-G

http://identifiers.org/hco/13/GRCh38#95528511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#119069983-C-A

95528577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119070055-G-A

95528577-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119070055-G-C

95528577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119070055-G-T

95528590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 119070068-G-A

95528590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 119070068-G-T

95528665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119070145-T-C

95528666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119070146-G-A

95528725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119070219-T-C

95528870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119070345-T-C

95529402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119070734-G-A

95529402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119070734-G-T

95529424-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119070756-G-C

95529496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119070825-G-T

95529689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119071005-T-C

95529762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119071089-T-C

95529808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119071132-G-T

95529979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119071598-T-C

95529985-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119071604-G-C

95530339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119071931-C-T

95530400-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119071992-C-G

95530532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119072127-G-A

95530648-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119072225-A-T

95530667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119072244-A-G

95530852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119072419-T-C

95530890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119072454-C-T

95530899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119072463-A-G

95530921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119072485-C-T

95531238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119072492-C-T

http://identifiers.org/hco/13/GRCh38#95531405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#119072642-C-A

95531405-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119072642-C-G

95531405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119072642-C-T

95531420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119072657-T-C

95533429-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119073039-T-G

95533651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119073315-C-T

http://identifiers.org/hco/13/GRCh38#95533693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#119073457-C-A

95533717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119073515-A-G

95533746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119073551-G-A

95533746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119073551-G-T

95533763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119073571-T-C

95533863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119073643-G-A

95533863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119073643-G-T

http://identifiers.org/hco/13/GRCh38#95533873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#119073650-C-A

http://identifiers.org/hco/13/GRCh38#95533896-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#119073668-C-A

http://identifiers.org/hco/13/GRCh38#95533913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#119073682-C-A

95533913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119073682-C-T

http://identifiers.org/hco/13/GRCh38#95533965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#119073719-C-A

95533965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119073719-C-T

http://identifiers.org/hco/13/GRCh38#95534021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#119073773-C-A

95534021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119073773-C-T

95534110-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119073864-G-T

http://identifiers.org/hco/13/GRCh38#95536088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#119074472-C-A

http://identifiers.org/hco/13/GRCh38#95536101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#119074478-C-A

95536176-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119074551-T-A

95536176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119074551-T-C

95536180-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119074555-T-A

95536180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119074555-T-C

95536496-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119074628-C-G

http://identifiers.org/hco/13/GRCh38#95536509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#119074641-C-A

95536619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119074769-G-T

95536753-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119074895-C-G

95536753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119074895-C-T

95536964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119075095-T-C

95536964-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119075095-T-G

http://identifiers.org/hco/13/GRCh38#95537080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#119075197-C-A

95537243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119075339-C-T

95537247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119075343-C-T

95537288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119075389-G-T

95537351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119075625-T-C

95537419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119075690-C-T

95537585-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119075824-A-T

95537589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119075828-G-A

95540672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119076612-G-A

95540785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119076779-G-T

95541176-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119077171-A-T

95541243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119077241-G-A

95541282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119077279-C-T

95541300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119077292-C-T

95541859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119078891-T-C

95542342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119078944-G-A

http://identifiers.org/hco/13/GRCh38#95542411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#119079009-C-A

95542411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119079009-C-T

http://identifiers.org/hco/13/GRCh38#95542448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#119079043-C-A

95542448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119079043-C-T

95543372-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119079542-G-C

http://identifiers.org/hco/13/GRCh38#95543900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#119080898-C-A

95544177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119081159-T-C

95544187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119081169-T-C

95544484-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119081481-T-A

95544484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119081481-T-C

95544558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119081550-T-C

95544596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119081582-A-G

http://identifiers.org/hco/13/GRCh38#95544694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#119081675-C-A

95544694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119081675-C-T

95545092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119082723-T-C

95545120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119082754-T-C

95545168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119082802-A-G

95545226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119082856-T-C

95545798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119085600-G-A

95545831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119085630-G-T

95545842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119085641-G-T

95547549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119086596-A-G

95547562-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119086609-C-G

95547620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119086661-A-G

95547805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119086814-A-G

95547808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119086817-T-C

95547912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119087296-A-G

95547934-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119087318-T-G

95548023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119087388-C-T

http://identifiers.org/hco/13/GRCh38#95548188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#119087556-C-A

95548351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119087693-G-A

95548632-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119088027-A-T

95548661-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119088042-C-G

95548911-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119088289-G-C

95549208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119088575-C-T

95549472-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119088774-T-G

95549481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119088783-T-C

95549501-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119088803-C-G

http://identifiers.org/hco/13/GRCh38#95549579-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#119088877-A-C

95549579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119088877-A-G

95549636-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119088930-T-G

95549682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119088967-A-G

http://identifiers.org/hco/13/GRCh38#95550209-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#119089475-A-C

95550443-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119089705-T-A

95550769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119089901-G-A

95550769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119089901-G-T

95550812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119089925-G-A

95551012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119089994-A-G

95551438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119090390-C-T

95551873-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119090833-G-C

95552043-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119091709-T-A

95552222-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119091866-C-G

95552517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119092185-G-A

95552517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119092185-G-T

http://identifiers.org/hco/13/GRCh38#95552585-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#119092260-A-C

95552636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119092294-G-A

95552636-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119092294-G-C

95552636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119092294-G-T

95552658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119092308-G-A

95552658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119092308-G-T

http://identifiers.org/hco/13/GRCh38#95552698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#119092348-C-A

95552698-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119092348-C-G

95552698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119092348-C-T

95552708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119092358-G-A

95552708-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119092358-G-C

95552708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119092358-G-T

95552736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 119092386-G-A

95552825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 119092473-G-A

95552897-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: 119092545-C-G

95553010-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 119092658-T-A

http://identifiers.org/hco/13/GRCh38#95553053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#119092698-C-A

http://identifiers.org/hco/13/GRCh38#95553065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#119092710-C-A

95553065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 119092710-C-T

http://identifiers.org/hco/13/GRCh38#95553093-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#119092731-C-A

95553101-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 119092743-T-A

95553101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 119092743-T-C

95553283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 119092873-G-A

95553449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 119092990-C-T

95553614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 119093130-T-C

http://identifiers.org/hco/13/GRCh38#95553693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#119093217-C-A

95554091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 119093747-C-T

95554242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 119093896-G-A

95554718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 119094345-G-T

95555006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 119094564-A-G

95555764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 119094947-T-C

95555794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 119094982-T-C

95555888-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 119095095-G-T

95555948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119095161-G-T

95555988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119095193-A-G

95556413-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119095278-T-G

http://identifiers.org/hco/13/GRCh38#95556676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#119095473-C-A

95556684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119095487-G-A

95556706-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119095505-T-G

95556783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119095539-C-T

95556796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119095552-A-G

95556899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119095611-A-G

95557010-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119095712-G-C

95557018-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119095720-T-G

95557335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119096030-G-A

95557394-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119096090-T-A

95557558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 119096249-T-C

95557645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119096321-G-A

95557786-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119096444-C-G

95557797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119096455-T-C

95557985-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119096634-C-G

95558334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119097651-G-A

95558364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119097681-G-A

95558593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119097862-G-T

95558607-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119097876-C-G

95558628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119097898-A-G

95559023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119097977-G-A

95559023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119097977-G-T

95559119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119098072-G-A

95559170-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119098100-T-G

95559248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119098173-T-C

95559694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119098598-C-T

95559766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119098629-T-C

95559789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119098642-T-C

95559789-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119098642-T-G

95559790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119098643-C-T

95559840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119098692-C-T

95559856-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119098708-C-G

95559958-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119098797-T-A

95559994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119098833-T-C

95560056-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119099031-T-A

95560056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119099031-T-C

95560068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119099042-A-G

95560070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119099044-G-A

95560322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119099301-T-C

http://identifiers.org/hco/13/GRCh38#95560449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#119099428-C-A

http://identifiers.org/hco/13/GRCh38#95560621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#119099569-C-A

95560669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 119099615-T-C

http://identifiers.org/hco/13/GRCh38#95560690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#119099636-C-A

95560691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 119099637-A-G

http://identifiers.org/hco/13/GRCh38#95560710-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#119099656-A-C

95560710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 119099656-A-G

95560710-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 119099656-A-T

http://identifiers.org/hco/13/GRCh38#95560737-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#119099679-A-C

95560737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 119099679-A-G

95560767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 119099711-T-C

95560770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 119099714-C-T

95560771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 119099715-A-G

95560771-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 119099715-A-T

http://identifiers.org/hco/13/GRCh38#95560818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#119099752-C-A

95560818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 119099752-C-T

95560828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 119099762-T-C

http://identifiers.org/hco/13/GRCh38#95560978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#119099851-C-A

95560978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119099851-C-T

95560998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119099870-G-A

http://identifiers.org/hco/13/GRCh38#95561008-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#119099880-A-C

95561008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119099880-A-G

http://identifiers.org/hco/13/GRCh38#95561025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#119099892-C-A

95561025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119099892-C-T

95561120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119099991-G-A

95561278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119100183-T-C

95561279-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119100184-A-T

95561324-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119100227-T-G

95561397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119100292-G-A

95561666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119100487-C-T

http://identifiers.org/hco/13/GRCh38#95561679-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#119100499-A-C

95561747-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119100595-A-T

95562451-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119100678-T-G

http://identifiers.org/hco/13/GRCh38#95563889-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#119101181-A-C

95564084-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119101367-G-C

95564266-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119101553-T-G

95564282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119101570-G-A

95564318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119101606-A-G

95564551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119101844-G-A

95564557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119101850-T-C

95564689-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119101979-T-A

95565031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119102278-G-A

95565166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119102415-G-A

95565166-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119102415-G-C

95565221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119102458-C-T

95567968-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119102995-C-G

http://identifiers.org/hco/13/GRCh38#95568217-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#119103162-A-C

95568218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119103163-G-T

95568233-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119103182-A-T

95568324-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119103264-C-G

95568324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119103264-C-T

95568325-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119103265-A-T

95568414-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119103356-C-G

95568579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119103501-G-T

95568586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119103508-C-T

95568767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119103684-G-A

http://identifiers.org/hco/13/GRCh38#95568801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#119103704-C-A

95568843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119103750-G-A

95568918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119103851-C-T

95568997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119103911-G-A

http://identifiers.org/hco/13/GRCh38#95569203-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#119104089-A-C

95569203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119104089-A-G

95569221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119104107-G-A

http://identifiers.org/hco/13/GRCh38#95569230-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#119104116-A-C

95570070-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119104808-C-G

95570079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119104817-G-A

95570079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119104817-G-T

http://identifiers.org/hco/13/GRCh38#95570096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#119104834-C-A

95570153-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119104888-A-T

95570247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119104957-A-G

95570258-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119104968-T-G

95570608-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119105298-G-T

95570941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119105476-G-A

95570969-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119105482-G-C

95571174-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119105663-C-G

95571243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119105726-T-C

95571365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119105846-G-A

95571462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119105929-T-C

95571534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119105977-G-A

95571551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119105995-G-A

95571806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119106246-T-C

95571807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119106247-A-G

95571876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119106337-T-C

95572098-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119106483-A-T

95572433-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119106774-A-T

95572787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119107105-C-T

http://identifiers.org/hco/13/GRCh38#95572987-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#119107286-A-C

95573400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron_variant, undefined
orthologous variants: 119107692-G-A

95573437-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119107733-G-C

95573459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119107755-A-G

95574345-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119108106-T-A

95575081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119109145-A-G

95575393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119109400-G-A

95575972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119109859-C-T

95576153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119110007-T-C

95576182-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119110049-C-G

95576301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119110162-G-A

95576656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119110506-G-T

95576766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119110576-C-T

95576884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119110727-C-T

95577088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119110905-G-T

http://identifiers.org/hco/13/GRCh38#95577135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#119110951-C-A

95577135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119110951-C-T

95577193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119110977-T-C

95577212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119110996-G-A

95577238-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: missense variant
orthologous variants: 119111020-T-A

95577238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: synonymous variant
orthologous variants: 119111020-T-C

95577312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: synonymous variant
orthologous variants: 119111094-A-G

95577327-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: missense variant
orthologous variants: 119111109-C-G

95577327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: synonymous variant
orthologous variants: 119111109-C-T

95577421-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119111188-T-G

95577423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119111190-A-G

95577429-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119111196-T-G

http://identifiers.org/hco/13/GRCh38#95577474-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#119111237-C-A

95577474-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119111237-C-G

95577539-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119111304-T-G

95577789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119111505-G-A

http://identifiers.org/hco/13/GRCh38#95577855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#119111559-C-A

95577855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: intron variant
orthologous variants: 119111559-C-T

http://identifiers.org/hco/13/GRCh38#95578038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#119111748-C-A

95578038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: 3 prime UTR variant
orthologous variants: 119111748-C-T

95578044-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: 3 prime UTR variant
orthologous variants: 119111755-T-A

95578090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: 3 prime UTR variant
orthologous variants: 119111801-T-C

95578199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: 3 prime UTR variant
orthologous variants: 119111899-T-C

95578240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: 3 prime UTR variant
orthologous variants: 119111942-T-C

95578273-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: 3 prime UTR variant
orthologous variants: 119111970-G-C

95578273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: 3 prime UTR variant
orthologous variants: 119111970-G-T

95578369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: 3 prime UTR variant
orthologous variants: 119112047-T-C

95578448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: 3 prime UTR variant
orthologous variants: 119112127-T-C

95578475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: 3 prime UTR variant
orthologous variants: 119112156-G-T

http://identifiers.org/hco/13/GRCh38#95578483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#119112164-C-A

95578483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: 3 prime UTR variant
orthologous variants: 119112164-C-T

95578888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: 3 prime UTR variant
orthologous variants: 119112253-T-C

95579401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: 3 prime UTR variant
orthologous variants: 119112584-T-C

95579481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: 3 prime UTR variant
orthologous variants: 119112663-G-T

95579578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2033
most severe consequence: 3 prime UTR variant
orthologous variants: 119112738-T-C