108505540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 53292354-G-T

108505804-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 53292110-T-A

108505976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 53291932-G-A

108506248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 53291681-T-C

http://identifiers.org/hco/11/GRCh38#108507804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#53290521-C-A

108507834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 53290506-A-G

108508100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 53290241-A-G

http://identifiers.org/hco/11/GRCh38#108508101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#53290240-C-A

108508101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 53290240-C-T

108508110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 53290231-A-G

http://identifiers.org/hco/11/GRCh38#108508138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#53290199-C-A

108508138-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 53290199-C-G

108508139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 53290198-A-G

108508139-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 53290198-A-T

108508488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 53289833-C-T

http://identifiers.org/hco/11/GRCh38#108508494-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#53289827-A-C

108508494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 53289827-A-G

108508649-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 53289690-C-G

108508746-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 53289612-C-G

108508814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 53289542-G-A

http://identifiers.org/hco/11/GRCh38#108508865-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#53289509-A-C

108508865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 53289509-A-G

108508929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 53289445-T-C

108508970-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 53289330-A-T

108509040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 53289273-A-G

108509113-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 53289208-G-C

108509149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 53289171-T-C

108509223-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 53289108-T-G

108509241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 53289092-G-A

108509241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 53289092-G-T

108509264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 53289071-G-A

108509264-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 53289071-G-C

108509264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 53289071-G-T

108509338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 53288981-T-C

http://identifiers.org/hco/11/GRCh38#108509361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#53288958-C-A

108509361-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 53288958-C-G

108509430-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 53288920-A-T

108509649-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 53288680-C-G

108509900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 53288432-C-T

108509910-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 53288422-T-G

http://identifiers.org/hco/11/GRCh38#108509950-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#53288379-A-C

108509950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 53288379-A-G

108509965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 53288364-T-C

108510042-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 53288287-T-A

108510055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 53288274-G-A

108510055-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 53288274-G-C

108510055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 53288274-G-T

108510128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 53288201-A-G

108510324-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 53288017-T-G

108510362-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 53287994-A-T

108510392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 53287964-G-A

108510393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 53287963-T-C

108510400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 53287956-A-G

108510465-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 53287891-C-G

108510493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 53287863-G-A

108510519-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 53287837-C-G

http://identifiers.org/hco/11/GRCh38#108510597-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#53287771-A-C

108510677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 53287691-T-C

http://identifiers.org/hco/11/GRCh38#108510814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#53287560-C-A

108510814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 53287560-C-T

108510815-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 53287559-C-G

108510972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 53287417-G-A

108511021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 53287368-T-C

108511103-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 53287286-T-A

108511224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 53287177-G-A

108511243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 53287158-T-C

108511288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 53287113-C-T

108511417-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, stop_gained, undefined
orthologous variants: 53286984-T-A

108511550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 53286842-G-A

108511550-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 53286842-G-C

108511576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 53286816-A-G

108511576-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 53286816-A-T

108511608-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 53286784-T-A

108511639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 53286753-G-A

108511900-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 53286492-A-T

108512056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 53286348-C-T

108512184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 53286220-G-A

108512273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 53286143-C-T

http://identifiers.org/hco/11/GRCh38#108512373-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#53286049-A-C

108512451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 53285971-T-C

108512531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 53285894-T-C

108512533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 53285892-T-C

http://identifiers.org/hco/11/GRCh38#108512664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#53285770-C-A

108512670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 53285764-T-C

108512891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 53285564-G-T

108512903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 53285552-A-G

108513225-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 53285179-G-C

108513225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 53285179-G-T

108513291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 53285113-A-G

108513352-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 53285052-G-C

108513417-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 53284990-A-T

108513447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 53284960-T-C

108513517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 53284890-G-A

108513610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, stop_gained, undefined
orthologous variants: 53284797-G-A

http://identifiers.org/hco/11/GRCh38#108513619-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#53284788-A-C

108513635-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 53284772-T-G

http://identifiers.org/hco/11/GRCh38#108513655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, stop_gained, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#53284752-C-A

108513698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 53284709-A-G

108513726-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 53284681-G-C

http://identifiers.org/hco/11/GRCh38#108513804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#53284603-C-A

108513804-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 53284603-C-G

108513804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 53284603-C-T

http://identifiers.org/hco/11/GRCh38#108513848-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#53284559-A-C

108513848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 53284559-A-G

http://identifiers.org/hco/11/GRCh38#108513851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#53284556-C-A

108513851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 53284556-C-T

108513876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 53284531-C-T

108513883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 53284524-A-G

108513897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 53284510-T-C

108514012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 53284395-A-G

108514047-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 53284360-T-G

108514059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 53284348-T-C

108514197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 53284213-A-G

108514250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 53284160-A-G

108514306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 53284104-C-T

108514330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 53284080-A-G

108514330-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 53284080-A-T

108514512-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 53283898-G-C

108514809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 53283607-G-A

108514816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 53283600-T-C

108514910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, undefined
orthologous variants: 53283509-T-C

108515188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, undefined
orthologous variants: 53281585-G-A

108515363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, undefined
orthologous variants: 53281402-A-G

108515468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, undefined
orthologous variants: 53281267-A-G

108515481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, undefined
orthologous variants: 53281254-A-G

108515525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, undefined
orthologous variants: 53281228-T-C

108516636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, undefined
orthologous variants: 53279842-G-A

108517026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, undefined
orthologous variants: 53279521-G-A

108517527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, undefined
orthologous variants: 53278957-G-A

108517545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, undefined
orthologous variants: 53278933-C-T

108517583-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, undefined
orthologous variants: 53278895-T-G

108517656-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, undefined
orthologous variants: 53278844-T-G

108518198-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53278546-T-A

108518213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53278532-G-A

108518264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: missense variant
orthologous variants: 53278481-G-A

108518274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: missense variant
orthologous variants: 53278471-G-A

108518274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: missense variant
orthologous variants: 53278471-G-T

108518285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: missense variant
orthologous variants: 53278460-C-T

108518332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 53278413-A-G

108518424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53278319-A-G

108518430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53278313-T-C

108518467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53278286-A-G

108518468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53278285-T-C

108519607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53277452-G-A

http://identifiers.org/hco/11/GRCh38#108521605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53276512-C-A

108522227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53275380-A-G

108522337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53275270-A-G

108522365-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53275242-A-T

108522465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53275170-T-C

108522562-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53275078-T-A

108522597-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53275043-T-G

http://identifiers.org/hco/11/GRCh38#108522758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53274926-C-A

108522838-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53274861-T-G

108523231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53269226-A-G

108523447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53269004-A-G

108523458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53268993-T-C

108523504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53268947-A-G

108523603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53268834-G-A

108523707-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53268749-A-T

108523955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53268672-T-C

108525428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53267077-C-T

108525438-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53267068-C-G

108525714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53266728-A-G

108525898-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53266532-T-A

108525898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53266532-T-C

108525899-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53266531-A-T

http://identifiers.org/hco/11/GRCh38#108526057-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53266416-A-C

108526061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53266412-T-C

108527486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53265369-C-T

108527593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53265269-G-A

108527723-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53264916-G-C

108527985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53264649-T-C

108527997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53264637-G-T

http://identifiers.org/hco/11/GRCh38#108528013-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53264621-A-C

108528013-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53264621-A-T

108528096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53264540-T-C

108528096-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53264540-T-G

108528171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 53264465-C-T

108528178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 53264458-A-G

108528204-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53264432-T-G

108528207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53264429-T-C

108528306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53264325-G-A

108528306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53264325-G-T

108528530-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53264138-T-G

108528536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53264132-T-C

108528543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53264125-C-T

108528649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53264008-G-A

108529028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53263972-G-A

108529309-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53263718-G-C

108529956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53263357-G-A

108530140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53263187-T-C

108530547-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53260852-G-C

108530619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53260779-G-T

108530622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53260776-G-A

108530723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53260682-A-G

http://identifiers.org/hco/11/GRCh38#108530748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53260657-C-A

108530797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53260619-C-T

http://identifiers.org/hco/11/GRCh38#108530835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53260586-C-A

108531473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53259957-G-A

http://identifiers.org/hco/11/GRCh38#108531493-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53259937-A-C

108531662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53259779-T-C

108531815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53259671-G-A

108531815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53259671-G-T

108531879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53259613-C-T

108532120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53259448-A-G

108534473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53257856-T-C

108534473-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53257856-T-G

108534475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53257854-C-T

108534648-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53257723-C-G

108534684-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53257684-C-G

108534696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53257673-G-A

108535199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53257046-A-G

108537060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53254060-A-G

108537174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53253962-C-T

108537359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53253638-A-G

108537438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53253533-C-T

108537638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53253167-A-G

108537644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53253161-T-C

108537787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53252967-A-G

108537789-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53252965-A-T

108537860-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53252888-T-A

108537860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53252888-T-C

108537999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 53252735-A-G

http://identifiers.org/hco/11/GRCh38#108538085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53252671-C-A

108538086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 53252670-C-T

108538116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 53252643-G-A

108538116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 53252643-G-T

http://identifiers.org/hco/11/GRCh38#108538142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53252617-C-A

108538242-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53252516-C-G

108538242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53252516-C-T

http://identifiers.org/hco/11/GRCh38#108538615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53252171-C-A

108538698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53252115-A-G

108538821-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53251992-G-C

108538902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53251915-T-C

http://identifiers.org/hco/11/GRCh38#108539029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53251791-C-A

http://identifiers.org/hco/11/GRCh38#108539033-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53251787-C-A

108539068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 53251752-T-C

108539188-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: splice acceptor variant
orthologous variants: 53251638-T-A

108539188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: splice acceptor variant
orthologous variants: 53251638-T-C

http://identifiers.org/hco/11/GRCh38#108539465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53251029-C-A

108539534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53250966-C-T

108539550-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53250950-T-A

http://identifiers.org/hco/11/GRCh38#108539563-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53250938-A-C

108539563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53250938-A-G

108539570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53250932-A-G

108540716-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53250189-C-G

108540918-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53250009-A-T

108540924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53250003-G-A

108540925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53250002-G-T

108541014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53249923-C-T

108541032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53249905-G-A

108541094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53249848-G-T

108541101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53249841-C-T

108541485-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53249462-T-A

108541500-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53249440-A-T

http://identifiers.org/hco/11/GRCh38#108541549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53249398-C-A

108541549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53249398-C-T

108541798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 53249144-G-T

108542605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53248686-A-G

http://identifiers.org/hco/11/GRCh38#108542726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53248599-C-A

108543226-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53248407-C-G

108543547-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 53248173-C-G

108543618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53247961-G-A

108543752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53247832-C-T

108543795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53247781-C-T

108544467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53247436-C-T

108544668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53247270-A-G

108544803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53247148-T-C

108545406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53246805-C-T

http://identifiers.org/hco/11/GRCh38#108545460-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53246751-A-C

108545488-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53246725-T-A

108546070-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53246470-G-C

108546079-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53246460-G-C

108546165-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53246363-G-C

108546283-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53246239-T-A

108546283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53246239-T-C

108547462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53245629-A-G

108547700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53245388-T-C

108548722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53244773-C-T

108548793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53244711-A-G

108548889-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53244612-A-T

108548981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53244529-C-T

108558998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53240305-A-G

108559199-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53240124-A-T

108559495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53239931-G-A

http://identifiers.org/hco/11/GRCh38#108559654-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53239771-A-C

108559780-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53239656-G-C

108560144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53239363-A-G

108560241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53239279-C-T

108560895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53238605-A-G

108561114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53238414-G-A

http://identifiers.org/hco/11/GRCh38#108561383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53237419-C-A

http://identifiers.org/hco/11/GRCh38#108561419-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53237384-A-C

108561419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53237384-A-G

http://identifiers.org/hco/11/GRCh38#108561505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53237321-C-A

108561567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53237265-C-T

108561599-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53237233-T-G

108562017-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53236848-C-G

108562017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53236848-C-T

108562019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53236846-T-C

http://identifiers.org/hco/11/GRCh38#108562021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53236844-C-A

108562250-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53236637-T-G

http://identifiers.org/hco/11/GRCh38#108564562-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53236046-A-C

108564562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53236046-A-G

108564562-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53236046-A-T

108564705-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53235905-C-G

108564743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53235867-C-T

108565267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53235433-T-C

108565322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53235374-G-A

108565322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53235374-G-T

108565380-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53235325-C-G

108565410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53235301-C-T

108565763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53234963-C-T

108565853-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53234875-C-G

108565887-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53234820-T-A

108566057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53234650-G-T

108566070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53234637-A-G

108566086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53234625-T-C

108566164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53234575-T-C

http://identifiers.org/hco/11/GRCh38#108567380-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53233925-A-C

http://identifiers.org/hco/11/GRCh38#108567384-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53233921-A-C

108567384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53233921-A-G

108567472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53233824-C-T

108567587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53233582-G-A

http://identifiers.org/hco/11/GRCh38#108567756-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53233415-A-C

108567826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53233356-C-T

http://identifiers.org/hco/11/GRCh38#108567952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53233231-C-A

108567952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 53233231-C-T

108567971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 53233210-G-T

108567976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 53233205-T-C

108567985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 53233196-T-C

108568011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 53233168-A-G

108568040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 53233139-G-A

108568040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 53233139-G-T

http://identifiers.org/hco/11/GRCh38#108568052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53233128-C-A

108568107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 53233080-G-A

108568107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 53233080-G-T

108568116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 53233070-A-G

108568155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53233035-A-G

108568185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53232994-G-T

108568234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53232948-G-T

108568296-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53232888-G-C

108568337-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53232847-T-A

http://identifiers.org/hco/11/GRCh38#108568421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53232775-C-A

108568421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53232775-C-T

108568498-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53232700-C-G

108571066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53229591-G-A

108571087-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53229575-C-G

108571191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53229493-T-C

108571327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53229362-A-G

108571348-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53229342-G-C

108571502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53229245-G-A

108571523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53229226-C-T

108572117-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53227540-C-G

108586804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53219531-G-T

108586836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53219502-C-T

http://identifiers.org/hco/11/GRCh38#108586899-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53219438-A-C

108586899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53219438-A-G

108586922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53219409-G-A

108587451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53219075-G-T

108589930-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53216810-G-C

108589954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53216786-G-A

108590017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53216724-C-T

108590056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53216685-A-G

http://identifiers.org/hco/11/GRCh38#108591121-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53215811-A-C

108591160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53215774-G-A

108591334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53215635-C-T

108591343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53215626-A-G

108591463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53215535-C-T

108591571-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53215437-C-G

108591857-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53214474-T-G

108591938-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53214400-C-G

108592278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, undefined
orthologous variants: 53214095-G-A

108592278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, undefined
orthologous variants: 53214095-G-T

108592418-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53213947-C-G

108592487-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53213900-C-G

http://identifiers.org/hco/11/GRCh38#108592488-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53213899-A-C

108592936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53213584-G-A

108592952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53213568-G-A

http://identifiers.org/hco/11/GRCh38#108593259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53213271-C-A

http://identifiers.org/hco/11/GRCh38#108593276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53213259-C-A

108593276-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53213259-C-G

108593546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 53213021-T-C

http://identifiers.org/hco/11/GRCh38#108593857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#53212725-C-A

108593857-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, undefined
orthologous variants: 53212725-C-G

108593857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, undefined
orthologous variants: 53212725-C-T

108593859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, undefined
orthologous variants: 53212723-G-A

108593859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, undefined
orthologous variants: 53212723-G-T

http://identifiers.org/hco/11/GRCh38#108593891-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#53212714-A-C

108594215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53212389-G-A

108594267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53212333-A-G

108594680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53212069-G-A

http://identifiers.org/hco/11/GRCh38#108596734-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53210226-A-C

108596950-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53210030-T-G

108597108-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30578
most severe consequence: intron variant
orthologous variants: 53209872-C-G