26917932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85653071-T-C

26918001-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85653131-G-T

26918050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85653181-T-C

26918076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85653207-G-A

26918128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85653270-T-C

http://identifiers.org/hco/21/GRCh38#26918400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#85653519-C-A

26918400-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85653519-C-G

26918569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85653721-G-T

http://identifiers.org/hco/21/GRCh38#26918612-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#85653764-A-C

26918660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85653812-A-G

26918660-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85653812-A-T

26918716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85653869-C-T

http://identifiers.org/hco/21/GRCh38#26918830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#85653967-C-A

26918830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85653967-C-T

26918842-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85653979-T-A

http://identifiers.org/hco/21/GRCh38#26918900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#85654029-C-A

26918900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85654029-C-T

http://identifiers.org/hco/21/GRCh38#26918929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#85654054-C-A

http://identifiers.org/hco/21/GRCh38#26918991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#85654093-C-A

26919036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85654127-C-T

http://identifiers.org/hco/21/GRCh38#26919073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#85654166-C-A

http://identifiers.org/hco/21/GRCh38#26919082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#85654175-C-A

26919100-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85654196-C-G

26919123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85654219-T-C

26919293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85654346-G-A

26919293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85654346-G-T

26919299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85654352-G-A

http://identifiers.org/hco/21/GRCh38#26919321-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#85654380-A-C

26919358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85654416-T-C

26919399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85654869-G-A

26919399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85654869-G-T

26919436-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85654904-T-A

26919436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85654904-T-C

26919465-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85654932-G-C

26919470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85654937-T-C

26919486-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85654953-A-T

http://identifiers.org/hco/21/GRCh38#26919551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#85655007-C-A

26919551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85655007-C-T

26919557-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85655013-C-G

26919557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85655013-C-T

26919624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85655069-G-T

http://identifiers.org/hco/21/GRCh38#26919625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#85655070-C-A

26919625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85655070-C-T

26919681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85655130-A-G

26919837-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85655283-C-G

http://identifiers.org/hco/21/GRCh38#26919986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#85655428-C-A

http://identifiers.org/hco/21/GRCh38#26920233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#85655673-C-A

26920343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85655801-A-G

26920551-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85655996-A-T

26920562-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85656007-T-G

26920589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85656033-G-A

26920776-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85656332-A-T

26920897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85656420-G-A

26920916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85656439-C-T

26921195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85656716-C-T

26921426-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85656936-T-G

26921459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85656962-T-C

26921459-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85656962-T-G

26921464-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85656967-T-A

26921497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85656989-A-G

26921497-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85656989-A-T

26921579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85657068-A-G

http://identifiers.org/hco/21/GRCh38#26921613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#85657102-C-A

26921613-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85657102-C-G

26921692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85657177-G-T

26921777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85657259-G-T

26921815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85657297-A-G

26921846-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85657326-A-T

26921903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85657386-G-A

26921903-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85657386-G-C

http://identifiers.org/hco/21/GRCh38#26922030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#85657504-C-A

26922031-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85657505-T-G

26922092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85657571-C-T

26922107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85657584-A-G

26922185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85657647-A-G

26922318-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85657774-G-C

26922477-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85657935-T-A

26922485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85657944-A-G

26922516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 85657973-G-A

26922624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85658084-G-A

26922752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85658160-C-T

http://identifiers.org/hco/21/GRCh38#26922789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#85658197-C-A

26922789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85658197-C-T

26922893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85658305-T-C

26922894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85658306-G-A

26922894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85658306-G-T

26922901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85658313-A-G

26922997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85658399-C-T

26923067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85658469-T-C

26923085-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85658487-T-G

26923112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85658519-A-G

26923226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85658638-T-C

26923308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85658721-G-A

26923308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85658721-G-T

26923443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85658900-G-T

26923843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85659292-G-T

26923877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85659325-G-A

26923877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85659325-G-T

26923928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85659373-T-C

26923946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85659391-G-T

http://identifiers.org/hco/21/GRCh38#26923992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#85659437-C-A

26923992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85659437-C-T

26924007-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85659452-T-A

26924024-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85659468-A-T

26924127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 85659572-G-A

26924127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 85659572-G-T

http://identifiers.org/hco/21/GRCh38#26924182-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#85659627-A-C

26924332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 85659777-G-A

26924332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 85659777-G-T

26924374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 85659819-A-G

26924485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 85659930-A-G

26924494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, stop_gained, undefined
orthologous variants: 85659939-G-T

26924597-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 85660042-C-G

26924755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85660201-G-A

26924755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85660201-G-T

26924918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85660370-T-C

26925029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85660496-C-T

26925277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85661218-G-A

26925529-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85661452-T-A

26925529-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85661452-T-G

26925572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85661495-G-A

26925572-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85661495-G-C

26925666-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85661620-T-G

26925951-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85661882-A-T

26925986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85661917-A-G

26928726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85661979-C-T

26928755-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85662014-A-T

26928819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85662077-G-A

26928924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85662186-T-C

26929012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85662259-G-A

26929019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85662266-A-G

26929039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85662285-T-C

26929625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85663256-G-T

26929687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85663316-A-G

26929706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85663335-C-T

26929819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85663441-T-C

26929871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85663493-G-A

26929882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85663504-T-C

26930064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant, undefined
orthologous variants: 85663686-G-T

http://identifiers.org/hco/21/GRCh38#26930116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#85663737-C-A

26930116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85663737-C-T

26930181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85663795-A-G

26930181-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85663795-A-T

http://identifiers.org/hco/21/GRCh38#26930376-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#85664244-C-A

26931655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85664573-C-T

26931733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85664647-G-T

26931856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85664750-A-G

26931896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85664789-A-G

26931899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85664792-G-T

http://identifiers.org/hco/21/GRCh38#26931933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#85664844-C-A

26931933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85664844-C-T

26932085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 85664995-A-G

26932203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85665114-A-G

26932498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85665225-T-C

26932725-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85665310-T-G

26932784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85665347-G-A

26932784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85665347-G-T

http://identifiers.org/hco/21/GRCh38#26932804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#85665367-C-A

26932880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 85665446-G-A

26932913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 85665479-T-C

http://identifiers.org/hco/21/GRCh38#26932985-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#85665551-A-C

26933011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 85665577-A-G

26933121-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85665680-A-T

26933134-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85665693-G-C

26933134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85665693-G-T

26933170-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85665709-T-A

26933170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85665709-T-C

26933273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85665796-C-T

26933275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85665798-T-C

26933535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85666057-C-T

26933638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85666168-C-T

26933641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85666171-T-C

26933655-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85666185-G-C

26933675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85666205-G-A

26933787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85666311-G-A

26933788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85666312-T-C

26934013-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85666403-T-G

26934170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85666522-A-G

http://identifiers.org/hco/21/GRCh38#26934316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#85666672-C-A

26934316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85666672-C-T

26934318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85666674-G-T

26934391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85666749-A-G

26934396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85666754-C-T

26934400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85666758-A-G

26934516-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 85666852-T-A

26934637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 85666973-G-A

26934637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 85666973-G-T

http://identifiers.org/hco/21/GRCh38#26934688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#85667024-C-A

26934688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 85667024-C-T

26934726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, stop_gained, undefined
orthologous variants: 85667062-G-A

26934807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85667143-T-C

26934807-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85667143-T-G

26934811-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85667147-G-C

26934823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85667159-G-A

26934823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85667159-G-T

http://identifiers.org/hco/21/GRCh38#26934880-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#85667187-C-A

26934917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85667217-C-T

26934971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85667262-C-T

26935508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85667736-T-C

26935892-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85668059-T-G

http://identifiers.org/hco/21/GRCh38#26936208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#85668370-C-A

26936722-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85668890-G-C

26936802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85668970-T-C

http://identifiers.org/hco/21/GRCh38#26936950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#85669139-C-A

26937053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85669248-T-C

26937249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85669362-T-C

26937471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85669528-T-C

26937685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85669752-C-T

26937693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85669760-G-A

26937753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85669820-G-A

26938949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85670386-T-C

26939091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85670512-C-T

26939564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85670908-C-T

26939611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant, undefined
orthologous variants: 85670948-C-T

http://identifiers.org/hco/21/GRCh38#26939801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85671133-C-A

26939861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 85671182-G-T

26939999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85671314-C-T

26940550-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85671849-T-G

http://identifiers.org/hco/21/GRCh38#26940687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85671947-C-A

26941012-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85672280-T-A

26941072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85672316-G-T

26941208-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85672449-C-G

http://identifiers.org/hco/21/GRCh38#26941456-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85672707-A-C

http://identifiers.org/hco/21/GRCh38#26941638-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85672886-A-C

http://identifiers.org/hco/21/GRCh38#26942282-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85673669-A-C

26942317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85673702-A-G

26942427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85673810-C-T

26942540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85673923-T-C

26942909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85674292-C-T

26943027-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85674404-T-G

26943076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85674453-T-C

26943250-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85674629-T-G

26943272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85674650-A-G

26943276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85674654-T-C

26943306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85674684-G-A

26943306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85674684-G-T

26943359-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85674737-G-C

26943381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant, synonymous_variant
orthologous variants: 85674759-A-G

26943381-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, splice_region_variant
orthologous variants: 85674759-A-T

26943384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 85674762-G-A

26943432-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 85674810-G-C

26943432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 85674810-G-T

26943453-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 85674831-G-C

26943478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 85674856-T-C

26943573-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85674954-A-T

26943583-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85674964-T-A

26943586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85674994-T-C

26943594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85675002-T-C

26943594-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85675002-T-G

26943626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85675034-T-C

26943661-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85675086-T-A

26943661-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85675086-T-G

http://identifiers.org/hco/21/GRCh38#26943671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85675096-C-A

26943671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85675096-C-T

26944155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85675553-A-G

26944155-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85675553-A-T

26944324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85675718-G-T

26944674-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85676019-C-G

26944674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85676019-C-T

26944703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85676045-A-G

26945124-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85676472-G-T

26945183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85676514-C-T

http://identifiers.org/hco/21/GRCh38#26945459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85676799-C-A

26945646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85676982-G-A

26945682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85677019-G-A

26945721-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85677050-T-A

26945917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85677246-A-G

26946025-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85677337-T-G

26946218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85677529-G-A

26946226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85677537-C-T

26946540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85677868-G-A

26946633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85677964-G-T

http://identifiers.org/hco/21/GRCh38#26946634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85677965-C-A

26946635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85677966-A-G

26946756-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85678089-C-G

26948103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85678577-C-T

26948514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85679309-G-A

26948754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85679545-T-C

26948793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85679569-T-C

http://identifiers.org/hco/21/GRCh38#26948920-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85679696-C-A

26949544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85680192-G-T

26949589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85680235-C-T

26949768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85680415-G-A

26949946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85680626-C-T

http://identifiers.org/hco/21/GRCh38#26950649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85681301-C-A

26950681-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85681344-T-A

26950697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85681360-G-A

http://identifiers.org/hco/21/GRCh38#26951293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85682237-C-A

26951334-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85682281-T-A

http://identifiers.org/hco/21/GRCh38#26951687-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85682423-A-C

http://identifiers.org/hco/21/GRCh38#26951688-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85682424-A-C

26951688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85682424-A-G

26951720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85682456-A-G

26951726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85682462-A-G

26951726-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85682462-A-T

http://identifiers.org/hco/21/GRCh38#26951815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85682526-C-A

26951815-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85682526-C-G

http://identifiers.org/hco/21/GRCh38#26952038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85682723-C-A

26952104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85682784-C-T

26952443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85683052-A-G

26952597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85683200-G-A

26953319-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85683415-C-G

26953410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85683490-G-A

http://identifiers.org/hco/21/GRCh38#26953456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85683549-C-A

26953456-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85683549-C-G

26953456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85683549-C-T

26953528-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85683612-A-T

26953831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85683890-T-C

26953856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85683908-G-T

26953891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85683943-G-A

26953891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85683943-G-T

26954034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85684022-G-T

26954076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85684061-T-C

http://identifiers.org/hco/21/GRCh38#26954095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85684080-C-A

26954580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85684546-G-A

26954622-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85684588-T-A

26954622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85684588-T-C

26954683-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85684649-G-C

26954683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85684649-G-T

26954695-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85684661-A-T

26954890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85684856-G-A

26955014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85684982-A-G

26955085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85685053-A-G

26955151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85685119-G-A

26955309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85685271-A-G

26955676-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85685832-A-T

26956228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85686310-T-C

26956517-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85686532-A-T

26956555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85686568-C-T

26957507-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85687294-T-G

http://identifiers.org/hco/21/GRCh38#26957620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85687450-C-A

26957658-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85687515-T-G

26957705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85687562-A-G

26957918-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85687758-T-A

http://identifiers.org/hco/21/GRCh38#26958017-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85687854-A-C

26958266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85688102-A-G

26958458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85688485-C-T

26958608-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85688631-G-T

26958671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85688694-G-T

26958699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85688723-T-C

26959037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85689045-G-A

http://identifiers.org/hco/21/GRCh38#26959142-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85689156-A-C

26959287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85689303-C-T

26959578-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85689594-T-G

26959674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85689692-C-T

26959748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85689769-C-T

http://identifiers.org/hco/21/GRCh38#26959802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85689861-C-A

26959850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85689906-G-A

26959850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85689906-G-T

26960021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85690070-T-C

26960079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85690128-C-T

26960236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85690274-C-T

26960319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85690318-A-G

26960379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85690380-G-A

26961411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85691768-T-C

26961515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85691867-C-T

26961630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85692024-T-C

26961661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85692054-A-G

26961761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85692133-G-A

26961764-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85692136-A-T

26961961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85692357-A-G

26962090-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85692491-G-C

26962208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85692607-G-A

26962208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85692607-G-T

26962294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85692687-G-A

26962336-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85692729-T-A

26962425-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85692814-T-G

26962667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85693057-G-A

26962667-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85693057-G-C

26962705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85693095-C-T

26962846-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85693242-C-G

26963129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85693526-G-T

26963148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85693544-T-C

26963397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85693990-G-A

26963620-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85694214-C-G

26963792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85694357-G-A

26963899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85694459-C-T

26964004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85694560-G-A

26964311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85695147-T-C

http://identifiers.org/hco/21/GRCh38#26964320-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85695156-A-C

26964320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85695156-A-G

26964797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85695602-G-T

26965012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85695781-C-T

26965114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85695877-G-A

http://identifiers.org/hco/21/GRCh38#26965120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85695883-C-A

26965145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85695908-G-A

26965145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85695908-G-T

26965198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85695965-T-C

http://identifiers.org/hco/21/GRCh38#26965220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85695987-C-A

26965259-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85696028-T-A

26965276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85696040-G-A

26965276-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85696040-G-C

26965350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 85696114-G-A

http://identifiers.org/hco/21/GRCh38#26965618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85696382-C-A

26965620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: missense_variant, undefined
orthologous variants: 85696384-G-A

26965620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: synonymous_variant, undefined
orthologous variants: 85696384-G-T

26965642-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: synonymous_variant, undefined
orthologous variants: 85696406-T-A

26965642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: synonymous_variant, undefined
orthologous variants: 85696406-T-C

26965642-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: synonymous_variant, undefined
orthologous variants: 85696406-T-G

http://identifiers.org/hco/21/GRCh38#26965732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: missense_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#85696496-C-A

26965732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: synonymous_variant, undefined
orthologous variants: 85696496-C-T

26965774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: synonymous variant
orthologous variants: 85696538-G-A

26965774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: synonymous variant
orthologous variants: 85696538-G-T

26965779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: missense variant
orthologous variants: 85696543-G-A

26965779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: missense variant
orthologous variants: 85696543-G-T

26965811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: missense_variant, undefined
orthologous variants: 85696575-G-A

26965891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: synonymous variant
orthologous variants: 85696649-T-C

26965891-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: synonymous variant
orthologous variants: 85696649-T-G

26965943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: missense variant
orthologous variants: 85696701-C-T

26966053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: synonymous variant
orthologous variants: 85696811-G-A

26966190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: missense variant
orthologous variants: 85696951-G-A

26966190-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: missense variant
orthologous variants: 85696951-G-C

26966210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: missense variant
orthologous variants: 85696971-G-A

26966210-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: missense variant
orthologous variants: 85696971-G-C

26966210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: missense variant
orthologous variants: 85696971-G-T

26966237-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: missense variant
orthologous variants: 85696986-T-A

26966237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: missense variant
orthologous variants: 85696986-T-C

26966238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: stop gained
orthologous variants: 85696987-G-A

26966238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: missense variant
orthologous variants: 85696987-G-T

http://identifiers.org/hco/21/GRCh38#26966271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85697020-C-A

26966271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: missense variant
orthologous variants: 85697020-C-T

26966288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: missense variant
orthologous variants: 85697037-G-A

26966288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: missense variant
orthologous variants: 85697037-G-T

26966321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: missense_variant, undefined
orthologous variants: 85697070-G-A

26966321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: missense_variant, undefined
orthologous variants: 85697070-G-T

http://identifiers.org/hco/21/GRCh38#26966337-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: missense_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#85697086-C-A

26966337-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: missense_variant, undefined
orthologous variants: 85697086-C-G

26966337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: missense_variant, undefined
orthologous variants: 85697086-C-T

http://identifiers.org/hco/21/GRCh38#26966373-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85697137-A-C

26966373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: missense variant
orthologous variants: 85697137-A-G

http://identifiers.org/hco/21/GRCh38#26966374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85697138-C-A

26966374-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: synonymous variant
orthologous variants: 85697138-C-G

26966374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: synonymous variant
orthologous variants: 85697138-C-T

26966474-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 5 prime UTR variant
orthologous variants: 85697239-A-T

http://identifiers.org/hco/21/GRCh38#26966542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85697347-C-A

26966542-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 5 prime UTR variant
orthologous variants: 85697347-C-G

26966542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 5 prime UTR variant
orthologous variants: 85697347-C-T

http://identifiers.org/hco/21/GRCh38#26966647-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85697448-A-C

26966647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 5 prime UTR variant
orthologous variants: 85697448-A-G

26966670-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 85697471-T-A

26966670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 85697471-T-C

26966670-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 85697471-T-G

http://identifiers.org/hco/21/GRCh38#26966686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#85697491-C-A

26966693-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 85697498-T-A

26966693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 85697498-T-C

26966740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 85697556-C-T

26966776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 85697613-C-T

26966786-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 85697620-G-C

26966827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 221
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 85697661-C-T