32720074-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: undefined
orthologous variants: 35236959-T-A

32726368-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35236080-C-G

32731580-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35228818-T-G

32731583-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35228815-G-C

http://identifiers.org/hco/19/GRCh38#32731629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35228768-C-A

32731629-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35228768-C-G

32731629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35228768-C-T

32731638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35228759-G-T

32731808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: synonymous variant
orthologous variants: 35228611-T-C

32731914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35228505-G-A

http://identifiers.org/hco/19/GRCh38#32731925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35228494-C-A

32731925-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35228494-C-G

32731925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35228494-C-T

32732613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35227569-C-T

32736663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35224463-G-A

32736678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35224448-A-G

32736743-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35224437-C-G

32736792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35224371-T-C

32738892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: missense variant
orthologous variants: 35223461-T-C

32738892-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: missense variant
orthologous variants: 35223461-T-G

32738995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35223358-A-G

http://identifiers.org/hco/19/GRCh38#32739056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35223297-C-A

32739056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35223297-C-T

32742723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35221520-C-T

32744539-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35214647-T-A

32744539-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35214647-T-G

32744717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35214495-C-T

32744748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35214464-G-A

32744781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35214445-G-A

32744844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35214388-A-G

32745020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35214214-G-A

32745051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35214170-A-G

32745358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35213874-A-G

32745358-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35213874-A-T

32747160-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35213051-G-C

32747205-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35213014-T-G

32747260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35212973-T-C

32748069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35211823-G-A

32748072-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35211820-T-A

32748094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35211805-G-A

32748096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35211804-G-A

http://identifiers.org/hco/19/GRCh38#32748128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35211772-C-A

32748151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35211749-G-A

32748190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35211700-A-G

32748227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35211631-A-G

32748244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35211609-G-T

32748428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35211458-T-C

32748453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35211433-G-A

32748453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35211433-G-T

32748520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: missense variant
orthologous variants: 35211366-A-G

http://identifiers.org/hco/19/GRCh38#32748554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35211334-C-A

32748554-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35211334-C-G

32748554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35211334-C-T

32748569-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35211319-T-A

32748569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35211319-T-C

http://identifiers.org/hco/19/GRCh38#32748575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35211313-C-A

32748575-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35211313-C-G

http://identifiers.org/hco/19/GRCh38#32748680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35211213-C-A

32748680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35211213-C-T

32748800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35211083-C-T

32748801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35211082-G-A

32749739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35210768-T-C

http://identifiers.org/hco/19/GRCh38#32755137-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35209697-A-C

32755160-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35209679-T-A

32755285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35209567-A-G

32755455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35209408-T-C

32755756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35208627-G-A

32755756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35208627-G-T

32755763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35208620-C-T

32755785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35208598-C-T

32755840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35208539-C-T

32755858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35208520-C-T

32755884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35208494-A-G

32755891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35208487-T-C

32755909-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35208476-T-G

32755910-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35208475-T-G

32755931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35208448-T-C

http://identifiers.org/hco/19/GRCh38#32755959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35208425-C-A

32755959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35208425-C-T

32756121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: missense variant
orthologous variants: 35208259-A-G

32756121-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: missense variant
orthologous variants: 35208259-A-T

32756272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35208142-A-G

32756276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35208138-A-G

32756313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35208092-A-G

32756313-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35208092-A-T

http://identifiers.org/hco/19/GRCh38#32756319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35208086-C-A

32756319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35208086-C-T

32756870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35207931-A-G

32757077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: missense variant
orthologous variants: 35207741-A-G

32772657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35204575-A-G

32772657-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35204575-A-T

32772660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35204572-A-G

32772699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35204543-T-C

http://identifiers.org/hco/19/GRCh38#32772754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: missense_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35204492-C-A

32772754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 35204492-C-T

http://identifiers.org/hco/19/GRCh38#32772759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35204487-C-A

32772759-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: missense variant
orthologous variants: 35204487-C-G

32772830-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: missense variant
orthologous variants: 35204419-T-A

32772957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35204315-A-G

32773037-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35204248-G-C

32773155-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35204157-T-G

32773156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35204156-G-A

http://identifiers.org/hco/19/GRCh38#32773158-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35204154-A-C

32773182-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35204129-T-G

32773284-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35204031-T-A

32773417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35203904-G-A

32773420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35203901-T-C

32773421-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35203900-A-T

32773506-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: stop gained
orthologous variants: 35203603-T-A

32773969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35202932-A-G

32777125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35200922-T-C

32777125-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35200922-T-G

32777132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35200915-T-C

32777132-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35200915-T-G

32777141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 35200901-A-G

32777141-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 35200901-A-T

32777280-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35200715-A-T

http://identifiers.org/hco/19/GRCh38#32777329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35200669-C-A

32777329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35200669-C-T

http://identifiers.org/hco/19/GRCh38#32777338-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35200660-C-A

32777338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35200660-C-T

32777357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35200641-A-G

32777370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35200628-G-A

32777370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35200628-G-T

32777428-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35200589-T-G

32777499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35200528-A-G

32777519-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35200507-T-A

32777572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35200453-T-C

32777605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35200411-T-C

32779675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35195420-T-C

32779809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35195292-G-A

32779856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35195241-G-A

32789723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35194470-G-A

32789746-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35194447-A-T

32789936-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35194328-A-T

32789954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35194318-A-G

32789982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35194289-A-G

32790014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35194269-A-G

32790028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35194255-G-A

32790030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35194253-G-A

32790149-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35194155-T-A

32790349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35193961-G-A

32790369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35193941-T-C

32790399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35193882-A-G

32790399-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35193882-A-T

32790429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35193858-T-C

32790429-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35193858-T-G

32790430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35193857-G-A

32790430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35193857-G-T

32790464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35193823-A-G

32790768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35193555-G-T

32790817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35193507-G-T

32790856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35193477-A-G

32790867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35193466-T-C

http://identifiers.org/hco/19/GRCh38#32790945-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35193377-A-C

32790953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35193370-C-T

32791176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35193033-T-C

32794849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35189326-G-A

32797579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35188922-A-G

32798242-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35188256-T-A

32798373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: missense variant
orthologous variants: 35188122-C-T

32798407-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: missense variant
orthologous variants: 35188088-A-T

32798410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: missense variant
orthologous variants: 35188085-T-C

32798410-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: missense variant
orthologous variants: 35188085-T-G

32798412-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: missense variant
orthologous variants: 35188083-C-G

32800299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: missense variant
orthologous variants: 35187014-G-A

32800299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: missense variant
orthologous variants: 35187014-G-T

32800350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: missense variant
orthologous variants: 35186963-G-A

32800376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35186942-T-C

32800379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35186939-A-G

32800389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35186929-G-A

32800389-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35186929-G-C

32800443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35186888-T-C

32800502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35186826-G-T

32800903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35186515-A-G

32800919-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35186500-T-A

32801220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35186364-A-G

32801405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35186233-T-C

32801421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35186218-T-C

32801579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35186086-C-T

32801695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35186021-A-G

http://identifiers.org/hco/19/GRCh38#32801720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35185996-C-A

32801720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35185996-C-T

32801916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35185806-T-C

32801917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35185805-A-G

32801919-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35185803-T-A

32801919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35185803-T-C

32802180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35185618-A-G

32802266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35185591-A-G

32802510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35185394-G-T

32802556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35185258-G-A

http://identifiers.org/hco/19/GRCh38#32802583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35185231-C-A

32802583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35185231-C-T

32802594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35185220-G-A

32802691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: missense variant
orthologous variants: 35185127-A-G

32802828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35184984-A-G

32802828-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35184984-A-T

32802832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35184980-T-C

32803007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: missense variant
orthologous variants: 35184763-T-C

32803168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35184610-A-G

32803266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35184497-G-A

32803266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35184497-G-T

http://identifiers.org/hco/19/GRCh38#32803279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35184484-C-A

32803279-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35184484-C-G

32806944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35183835-G-A

32806957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35183822-C-T

32806996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35183755-A-G

http://identifiers.org/hco/19/GRCh38#32807608-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35182503-A-C

http://identifiers.org/hco/19/GRCh38#32807678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35182436-C-A

32807678-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35182436-C-G

32807697-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35182410-A-T

32809947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35180761-G-A

32809947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35180761-G-T

http://identifiers.org/hco/19/GRCh38#32809976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35180732-C-A

32809976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35180732-C-T

32809984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35180724-A-G

32809985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35180723-G-A

32809985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35180723-G-T

32810202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: missense variant
orthologous variants: 35180518-A-G

32810214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: coding_sequence_variant, missense_variant
orthologous variants: 35180503-C-T

32810286-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35180431-T-G

32810333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35180385-G-A

32810333-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35180385-G-C

32810334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35180384-T-C

http://identifiers.org/hco/19/GRCh38#32810354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35180364-C-A

32810354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35180364-C-T

32810371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35180349-A-G

32810371-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35180349-A-T

32810430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35180279-T-C

32810470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35180243-C-T

32811083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35179856-T-C

32811083-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35179856-T-G

32811109-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35179830-T-G

32811272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: missense variant
orthologous variants: 35179712-A-G

32811299-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: missense variant
orthologous variants: 35179685-T-A

32811299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: missense variant
orthologous variants: 35179685-T-C

32811346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: missense variant
orthologous variants: 35179638-C-T

32811400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: missense variant
orthologous variants: 35179584-G-A

32811400-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: missense variant
orthologous variants: 35179584-G-C

32811400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: stop gained
orthologous variants: 35179584-G-T

32811532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35179462-A-G

32811533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35179461-G-A

http://identifiers.org/hco/19/GRCh38#32811555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35179434-C-A

32811555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35179434-C-T

32811991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35179076-G-A

32812402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35178741-A-G

32812538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35178626-G-A

32812538-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35178626-G-C

32812642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35178529-A-G

32812643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35178528-G-T

32812696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35178477-C-T

32813533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35177711-G-A

32813533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35177711-G-T

32813618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35177637-T-C

32813646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35177609-A-G

32813669-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35177584-A-T

32813691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: missense variant
orthologous variants: 35177562-G-T

32813928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35177361-G-T

32813967-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35177323-A-T

32814316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35176817-G-A

32814614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35176346-A-G

32814657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35176267-A-G

http://identifiers.org/hco/19/GRCh38#32814686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35176237-C-A

32815029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35175919-C-T

32815126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35175815-C-T

32815190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35175760-C-T

32815289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: intron variant
orthologous variants: 35175676-C-T

32815493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: missense variant
orthologous variants: 35175483-T-C

32815550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: missense variant
orthologous variants: 35175426-A-G

32820772-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35171020-G-C

32820801-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35170964-G-C

32820860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35170894-G-A

32820860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35170894-G-T

32820966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35170782-G-T

http://identifiers.org/hco/19/GRCh38#32820992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35170759-C-A

32821025-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant, synonymous_variant
orthologous variants: 35170732-C-G

32821103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: NMD_transcript_variant, missense_variant, synonymous_variant
orthologous variants: 35170651-G-A

32821167-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: NMD_transcript_variant, intron_variant, stop_gained
orthologous variants: 35170588-T-G

http://identifiers.org/hco/19/GRCh38#32821419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35170450-C-A

32821505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35170379-A-G

32821510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35170374-A-G

32826121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, synonymous_variant
orthologous variants: 35169720-G-A

32826142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, synonymous_variant
orthologous variants: 35169699-G-A

http://identifiers.org/hco/19/GRCh38#32826201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35169635-C-A

32826201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 35169635-C-T

32826280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 35169553-T-C

http://identifiers.org/hco/19/GRCh38#32826429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35169408-C-A

32826545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 35169293-A-G

32826565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 35169273-A-G

http://identifiers.org/hco/19/GRCh38#32826631-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35169206-A-C

32826631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35169206-A-G

http://identifiers.org/hco/19/GRCh38#32826667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35169171-C-A

32826667-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35169171-C-G

http://identifiers.org/hco/19/GRCh38#32826773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35169065-C-A

32826773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35169065-C-T

32826787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35169051-G-T

32826788-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35169050-T-A

32826788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35169050-T-C

32826927-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35168919-A-T

32827186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, splice_region_variant, synonymous_variant
orthologous variants: 35168593-G-A

32827186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, splice_region_variant, synonymous_variant
orthologous variants: 35168593-G-T

http://identifiers.org/hco/19/GRCh38#32827197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35168582-C-A

32827197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 35168582-C-T

32827215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 35168564-G-T

32827244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, stop_gained
orthologous variants: 35168532-G-T

32827258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 35168518-A-G

http://identifiers.org/hco/19/GRCh38#32827401-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35168227-A-C

32827401-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35168227-A-T

32827451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35168192-C-T

32827453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35168190-C-T

32827461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35168180-C-T

32827463-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35168178-T-A

32827463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35168178-T-C

32827541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35168099-G-T

32827718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35168430-G-A

32827718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35168430-G-T

32827832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35168272-T-C

32828008-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35167759-A-T

32828025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35167740-C-T

32828064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35167701-G-A

http://identifiers.org/hco/19/GRCh38#32828193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35167600-C-A

32828193-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35167600-C-G

32828241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35167582-T-C

32828242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35167581-G-A

32828324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35167519-G-T

http://identifiers.org/hco/19/GRCh38#32828346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35167497-C-A

32828346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35167497-C-T

32828493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35167397-G-A

32828538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35167354-T-C

32828593-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35167300-T-A

32828706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35167066-C-T

32828774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35166997-C-T

32828778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35166996-G-A

32828778-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35166996-G-C

32828778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35166996-G-T

32828779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35166995-T-C

32828912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35166884-G-A

32828912-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35166884-G-C

32828912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35166884-G-T

http://identifiers.org/hco/19/GRCh38#32828948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35166850-C-A

32829142-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35166701-G-C

32829530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25044
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35166420-G-A