http://identifiers.org/hco/2/GRCh38#148644553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#49341361-C-A

148644553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: 5 prime UTR variant
orthologous variants: 49341361-C-T

148644704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49341498-G-T

148644860-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49341655-T-A

148644860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49341655-T-C

148644860-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49341655-T-G

148644880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 49341675-G-A

148644880-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 49341675-G-C

148644880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 49341675-G-T

http://identifiers.org/hco/2/GRCh38#148644941-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#49341739-A-C

http://identifiers.org/hco/2/GRCh38#148645236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#49342037-C-A

148645236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49342037-C-T

http://identifiers.org/hco/2/GRCh38#148645279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#49342081-C-A

148645279-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49342081-C-G

148645279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49342081-C-T

http://identifiers.org/hco/2/GRCh38#148645299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#49342100-C-A

148645299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49342100-C-T

http://identifiers.org/hco/2/GRCh38#148645302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#49342103-C-A

148645302-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49342103-C-G

148645302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49342103-C-T

148645454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 49342253-G-A

148645454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 49342253-G-T

148645472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 49342272-G-A

148645520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 49342318-G-A

148645520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 49342318-G-T

148645582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49342378-T-C

148645619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron_variant, undefined
orthologous variants: 49342424-A-G

148645720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49342528-G-T

148645788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49342577-C-T

148645892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49342654-C-T

148645896-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49342658-C-G

148646024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49342802-C-T

148648820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49343340-A-G

148649175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49343590-T-C

148650640-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49344186-A-T

148650888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49344364-A-G

148650897-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49344373-G-C

148651020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49344498-G-T

148651334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49345126-C-T

148651466-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49345262-G-C

148651485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49345280-G-A

148651589-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49345374-G-C

148651697-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49345456-T-G

148651723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49345473-A-G

148651740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49345489-A-G

148651761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49345499-G-T

148651870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49345597-T-C

148651905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49345629-A-G

148652041-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49346419-C-G

148652109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49346488-G-A

148652109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49346488-G-T

148652198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49346548-C-T

148652266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49346603-A-G

148652270-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49346607-T-G

148652471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49346740-A-G

http://identifiers.org/hco/2/GRCh38#148652533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#49346796-C-A

http://identifiers.org/hco/2/GRCh38#148652538-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#49346801-A-C

148652624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49346876-A-G

148652649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49346899-A-G

148652957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49347175-A-G

148653007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49347198-A-G

148653095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49347268-T-C

148653376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49347523-A-G

148653487-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49347801-T-G

148653732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49348019-G-A

148653858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49348111-G-A

148653934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49348153-G-T

148655000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49348865-A-G

148655130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49348982-G-A

148655201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49349055-G-T

148655258-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49349114-G-C

148655536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49349504-G-A

148655603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49349572-T-C

148655693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49349678-A-G

148657302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49349825-A-G

148657313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49349832-G-A

148661139-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49353737-T-G

148661325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49353904-C-T

148661349-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49353917-G-C

http://identifiers.org/hco/2/GRCh38#148665204-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#49356676-A-C

148665339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49356799-A-G

148665524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49356976-A-G

148665525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49356977-T-C

148665589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49357035-T-C

148665643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49357077-T-C

148665643-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49357077-T-G

148680155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49375331-G-T

148680339-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49375508-T-A

148680531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49375706-A-G

148680606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49375776-G-A

148680635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49375805-G-T

148680642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49375812-G-A

148680792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49375957-G-A

148680792-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49375957-G-C

148680811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49375982-C-T

148681281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49376395-G-A

148681618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49376710-C-T

148690086-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49378577-G-T

148690223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 49378710-T-C

148690393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49378880-G-T

148690425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49378912-G-A

148690425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49378912-G-T

http://identifiers.org/hco/2/GRCh38#148690452-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#49378936-A-C

148690452-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49378936-A-T

http://identifiers.org/hco/2/GRCh38#148690545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#49379028-C-A

148691003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49379161-A-G

http://identifiers.org/hco/2/GRCh38#148691394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#49379600-C-A

148691394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49379600-C-T

148691396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49379602-G-A

148691396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49379602-G-T

148691428-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49379653-T-A

148691428-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49379653-T-G

148691573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron_variant, missense_variant
orthologous variants: 49379838-G-T

148692919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49380294-T-C

148692922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49380297-C-T

148692966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49380343-A-G

148692978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49380356-C-T

148693587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49380981-T-C

148693767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49381151-T-C

148694165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49381481-G-A

148694188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49381504-G-A

148694621-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49381965-C-G

http://identifiers.org/hco/2/GRCh38#148694703-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#49382039-A-C

148694940-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49382276-T-G

148695206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49382537-A-G

148695317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49382672-A-G

148695397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49382745-A-G

148695770-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49383244-A-T

http://identifiers.org/hco/2/GRCh38#148695808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#49383290-C-A

148696064-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49383518-T-G

148696075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49383528-A-G

148696108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49383566-G-A

148696148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49383603-G-A

148696148-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49383603-G-C

148696335-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49383650-A-T

148696572-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49383867-G-C

148696653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49384090-C-T

148696684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49384121-G-A

148696737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49384176-A-G

148723462-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49387427-C-G

148723899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49387733-C-T

148724081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49388032-G-A

http://identifiers.org/hco/2/GRCh38#148724128-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#49388076-A-C

148724314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49388215-G-A

148724804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49388599-G-A

148725021-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49388802-T-A

148725021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49388802-T-C

148725040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49388820-G-A

148725040-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49388820-G-C

148725125-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49388913-T-A

148725321-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49389109-C-G

148725342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49389130-T-C

http://identifiers.org/hco/2/GRCh38#148725499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#49389267-C-A

148725499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49389267-C-T

148725925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49389669-T-C

148726263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49390020-G-A

148726547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49390300-C-T

148726553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49390306-G-A

148726553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49390306-G-T

148726956-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49390618-T-A

148727029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49390710-C-T

http://identifiers.org/hco/2/GRCh38#148727130-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#49390781-A-C

148727224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49390852-A-G

148727224-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49390852-A-T

148727225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49390853-A-G

148727312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49390923-A-G

http://identifiers.org/hco/2/GRCh38#148727447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#49391176-C-A

148727679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49391370-T-C

148729325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49392907-A-G

148729406-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49392979-C-G

148729406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49392979-C-T

http://identifiers.org/hco/2/GRCh38#148730421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#49393927-C-A

148730574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49394067-G-A

148730624-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49394111-T-A

148730640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49394127-A-G

148730739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49394162-T-C

148730766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49394183-A-G

148730801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49394214-A-G

148731340-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49394678-T-A

148734443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49398079-A-G

148734582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49398210-A-G

http://identifiers.org/hco/2/GRCh38#148734958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#49398535-C-A

148738544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49399477-T-C

148739160-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49400063-T-A

148739333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49400241-A-G

148739563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49400422-A-G

148739625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49400483-A-G

148740133-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49401400-A-T

148740371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49401603-C-T

148740491-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49401724-G-C

148740509-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49401742-A-T

148740962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49402168-G-T

148741036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49402241-A-G

148743047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49402780-C-T

http://identifiers.org/hco/2/GRCh38#148743589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#49403192-C-A

148743589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49403192-C-T

148743752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: synonymous variant
orthologous variants: 49403357-A-G

148743812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49403445-A-G

148743852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49403528-G-T

148743859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49403548-G-T

http://identifiers.org/hco/2/GRCh38#148743888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#49403682-C-A

148743888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49403682-C-T

148744308-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49404050-A-T

148744328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49404069-C-T

148744622-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49404385-C-G

148744652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49404415-G-A

148744786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49404543-G-T

148744845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49404604-T-C

http://identifiers.org/hco/2/GRCh38#148744928-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#49404859-A-C

148744942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49404873-A-G

148744942-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49404873-A-T

http://identifiers.org/hco/2/GRCh38#148744969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#49404910-C-A

148744969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49404910-C-T

148744988-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49404928-T-G

148745543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49405583-A-G

148746322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49406348-G-T

148746338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49406367-C-T

148746517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49406505-G-A

148746626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49406600-T-C

148747192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49406981-T-C

148747623-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49407421-G-C

148747838-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49407638-T-G

148747912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49407731-A-G

http://identifiers.org/hco/2/GRCh38#148749904-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#49408568-A-C

148750342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49409022-G-A

148750638-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49409287-T-A

148750683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49409333-A-G

148750715-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49409370-G-C

148752319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49410619-G-A

148752357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49410656-A-G

148752703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49411873-A-G

148754139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49412695-G-A

148754139-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49412695-G-T

148754150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49412706-G-A

148754150-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49412706-G-C

148754201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49412742-A-G

148754385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49412833-G-T

148754565-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49413005-G-C

148754999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49413433-G-A

148755323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49413756-G-T

148756104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49414003-A-G

148756418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49414310-A-G

148756779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49414651-G-A

148756950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49414809-G-A

148756982-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49414838-T-G

148760873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49417392-T-C

148761093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49417596-T-C

148761225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49417881-G-T

148761690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49418779-G-T

148761750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49418827-G-A

148761951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49419028-A-G

http://identifiers.org/hco/2/GRCh38#148761952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#49419029-C-A

148761952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49419029-C-T

http://identifiers.org/hco/2/GRCh38#148762023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#49419054-C-A

148762078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49419116-G-A

148762078-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49419116-G-C

148762103-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49419146-A-T

148762214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49419460-A-G

148762217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49419463-T-C

148762362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49419581-A-G

148762477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49419708-T-C

148762620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49419976-T-C

148762828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49420181-G-A

148763836-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49420977-T-G

148763843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49420984-G-A

148764780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49421874-G-A

148766091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49422919-C-T

148766315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49423102-A-G

148766371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49423154-T-C

http://identifiers.org/hco/2/GRCh38#148767295-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#49423592-A-C

148767419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49423696-T-C

148767727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49423988-G-A

148767728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49423989-T-C

http://identifiers.org/hco/2/GRCh38#148768852-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#49425012-A-C

148768904-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49425046-G-C

148769096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49425215-A-G

148769099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49425218-A-G

148769146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 49425262-T-C

148769155-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: missense variant
orthologous variants: 49425271-T-G

148769156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: synonymous variant
orthologous variants: 49425272-G-A

148769216-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: missense variant
orthologous variants: 49425332-G-C

148769358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49425472-A-G

148769382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49425501-A-G

148770651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49426455-G-A

148770651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49426455-G-T

148770660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49426464-T-C

148770751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49426556-C-T

148770956-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49426751-C-G

148770956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49426751-C-T

148770982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49426776-A-G

148771036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 49426829-C-T

148771208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: missense variant
orthologous variants: 49427001-C-T

http://identifiers.org/hco/2/GRCh38#148771386-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#49427179-A-C

http://identifiers.org/hco/2/GRCh38#148771506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#49427319-C-A

148771506-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49427319-C-G

148771525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49427332-A-G

148771633-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49427430-T-A

148772245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49427885-C-T

http://identifiers.org/hco/2/GRCh38#148772335-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#49427983-A-C

148772335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49427983-A-G

148772414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49428109-T-C

148773465-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49429299-T-G

148774658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49430445-A-G

148774658-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49430445-A-T

http://identifiers.org/hco/2/GRCh38#148775271-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#49430698-A-C

148775500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49430903-A-G

148776609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49431472-C-T

148777222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49431609-C-T

http://identifiers.org/hco/2/GRCh38#148777438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#49431787-C-A

148777675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49432072-G-A

148778413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49432656-G-A

148778415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49432658-G-A

148778747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49433038-A-G

148778820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49433102-G-A

148779259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49433449-C-T

http://identifiers.org/hco/2/GRCh38#148779803-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#49433850-A-C

148779872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49433908-T-C

148780483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49434455-G-A

148780484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49434456-G-A

148780524-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49434480-T-G

148780562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49434519-T-C

148780694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49434633-T-C

http://identifiers.org/hco/2/GRCh38#148780844-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#49434854-A-C

148781269-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49435252-C-G

148781273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49435256-G-T

148781537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49435636-G-A

148781537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49435636-G-T

http://identifiers.org/hco/2/GRCh38#148781596-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#49435688-A-C

148781596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49435688-A-G

http://identifiers.org/hco/2/GRCh38#148781601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#49435693-C-A

148781794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49435871-T-C

148781808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49435885-G-A

148781808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49435885-G-T

148781994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49436009-A-G

148782909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49436589-G-T

148783067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49436736-G-T

148783171-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49436829-T-G

148783308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49436964-T-C

148783319-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49436975-T-G

148783438-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49437086-A-T

http://identifiers.org/hco/2/GRCh38#148783452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#49437097-C-A

148783765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49437626-G-A

148783765-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49437626-G-C

148783765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49437626-G-T

http://identifiers.org/hco/2/GRCh38#148783774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#49437634-C-A

148783774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49437634-C-T

148783842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49437698-G-A

148783911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49437757-T-C

148784007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49437818-C-T

148784208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49438021-C-T

http://identifiers.org/hco/2/GRCh38#148784231-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#49438040-A-C

148784282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49438085-T-C

http://identifiers.org/hco/2/GRCh38#148784612-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#49438387-A-C

148784615-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49438390-A-T

148784618-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49438391-G-C

148784651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49438424-A-G

148785009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 49438784-T-C

148785009-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 49438784-T-G

http://identifiers.org/hco/2/GRCh38#148785019-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#49438788-A-C

148785019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49438788-A-G

148785020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49438789-G-A

148785043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49438817-G-A

148785043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49438817-G-T

148785800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49439612-G-A

http://identifiers.org/hco/2/GRCh38#148786161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#49439809-C-A

148786161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49439809-C-T

148786197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49439842-T-C

148786199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49439844-A-G

148786213-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49439858-T-A

148786277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49439913-T-C

148786287-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron variant
orthologous variants: 49439923-T-G

148786302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 49439935-T-C

http://identifiers.org/hco/2/GRCh38#148786450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#49440084-C-A

148787139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: 3 prime UTR variant
orthologous variants: 49440771-T-C

148787190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: 3 prime UTR variant
orthologous variants: 49440822-A-G

148787409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24543
most severe consequence: 3 prime UTR variant
orthologous variants: 49441040-T-C