96194799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93146482-G-T

96194849-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93146428-C-G

96194849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93146428-C-T

96194920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93146380-C-T

96195610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93145764-G-T

96195976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93145375-G-A

http://identifiers.org/hco/12/GRCh38#96196086-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93145265-C-A

http://identifiers.org/hco/12/GRCh38#96196152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#93145175-C-A

http://identifiers.org/hco/12/GRCh38#96196387-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93144925-A-C

96196416-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93144892-G-C

96196421-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93144865-T-G

96196493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93144761-C-T

96196727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93144528-G-A

96196750-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93144477-T-G

96196768-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93144459-T-A

96197032-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93144175-G-C

96197343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93143727-C-T

96197430-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93143640-A-T

96197792-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93143289-T-A

96197792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93143289-T-C

96197960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93143122-C-T

96198220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93142886-A-G

96198593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93142475-C-T

96198729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93142339-C-T

96198793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93142276-T-C

96199178-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93141909-A-T

96199204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93141882-G-A

96199264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93141822-G-T

96199452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93141643-A-G

96201092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93140565-T-C

96201359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93140317-A-G

96203369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93139356-C-T

96203387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93139333-G-A

96203474-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93139246-C-G

96203606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93139132-A-G

96204073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93139002-C-T

96204163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93138941-T-C

96204864-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93138206-C-G

96204870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93138200-C-T

96204948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93138117-G-A

96204972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93138088-T-C

96204980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93138080-C-T

96204993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93138067-G-A

96204993-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93138067-G-C

96205090-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93137958-T-A

96205142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93137903-C-T

96205231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93137810-A-G

96205239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93137802-C-T

96205284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93137757-C-T

96206049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93137161-T-C

http://identifiers.org/hco/12/GRCh38#96206071-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93137139-A-C

96206094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93137092-C-T

96206142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93136964-C-T

96206198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93136861-A-G

96206650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93136416-T-C

96206682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93136390-G-A

96207164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93135782-A-G

96207311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93135668-A-G

96207782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93135149-A-G

96207935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93134993-T-C

96208086-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93134863-T-A

96208086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93134863-T-C

http://identifiers.org/hco/12/GRCh38#96208801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93134470-C-A

96208884-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93134403-G-C

96209003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93134268-A-G

96209104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93134170-G-A

96209104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93134170-G-T

96209110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93134169-A-G

96209112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93134167-G-A

96209112-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93134167-G-C

96209112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93134167-G-T

96209492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93133730-C-T

96210030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93133510-G-T

96211076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93132019-C-T

96211107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93131987-G-A

96211107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93131987-G-T

96211416-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93131455-T-A

96211581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93131330-T-C

96211651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93131260-C-T

96211989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93131053-T-C

http://identifiers.org/hco/12/GRCh38#96212065-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93130977-A-C

96212303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93130728-T-C

96212437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93130601-C-T

96212549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93130480-C-T

96212642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93130399-C-T

96212749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93130308-G-A

http://identifiers.org/hco/12/GRCh38#96212775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93130281-C-A

96212775-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93130281-C-G

96212777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93130279-G-A

96212777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93130279-G-T

96212779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93130277-G-A

96212846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93130195-G-A

96212846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93130195-G-T

96212861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93130180-G-A

96212861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93130180-G-T

96212901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93130152-C-T

http://identifiers.org/hco/12/GRCh38#96212909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93130144-C-A

96212909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93130144-C-T

96212978-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93130075-T-G

96213376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93129694-C-T

96213378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93129692-C-T

96213685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93129405-T-C

96213694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93129396-T-C

96215276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93128012-C-T

96216025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93127610-T-C

96216031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93127604-C-T

96216100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93127545-C-T

96216207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93127487-C-T

96216224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93127470-C-T

96216840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93126891-A-G

96216925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93126807-A-G

96219043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93124407-G-A

96219545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93123994-G-A

96219580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93123959-A-G

96219655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93123908-A-G

96219665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93123898-C-T

96219894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93123684-A-G

96219927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93123658-A-G

96220947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93123198-C-T

96221475-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93123001-C-G

96221475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93123001-C-T

96221776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93122762-C-T

96221829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93122702-C-T

96221870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93122660-G-A

96222158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93121923-A-G

96223298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93121071-T-C

http://identifiers.org/hco/12/GRCh38#96223500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93120901-C-A

96223500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93120901-C-T

96223503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93120898-T-C

http://identifiers.org/hco/12/GRCh38#96223798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93120594-C-A

http://identifiers.org/hco/12/GRCh38#96223802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93120590-C-A

96223802-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93120590-C-G

96223802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93120590-C-T

96223806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93120586-G-A

96223886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93120510-A-G

96224455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93119559-A-G

96224616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93119178-G-T

96225126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93118668-T-C

96225277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93118531-G-T

96227034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93116821-G-T

http://identifiers.org/hco/12/GRCh38#96227084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93116772-C-A

96227845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93116134-T-C

96230686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93114130-A-G

96230961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93113878-G-A

96230961-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93113878-G-C

96231048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93113780-G-A

96231146-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93113708-T-A

96231819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93113233-A-G

96231836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93113209-C-T

http://identifiers.org/hco/12/GRCh38#96231861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93113180-C-A

96231861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93113180-C-T

96232193-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93112840-G-C

96233447-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93112255-C-G

96233447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93112255-C-T

96233714-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93111984-A-T

96233920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93111831-A-G

96234146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93111599-G-A

96234300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93111463-G-A

96234300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93111463-G-T

96234349-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 93111416-C-G

96234349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 93111416-C-T

96234373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93111392-A-G

96234793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93111010-G-A

96234848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93110971-C-T

96235050-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93110766-C-G

96235118-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93110526-C-G

96235186-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93110466-T-G

96235267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93110402-C-T

96235332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93110339-G-A

96235332-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93110339-G-C

96235378-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93110303-G-C

96236386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93109064-G-A

96236386-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93109064-G-C

96236419-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93109031-T-G

96236667-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93108794-C-G

96236770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93108714-C-T

96236983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93108511-C-T

96237188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93108318-A-G

96237188-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93108318-A-T

96237609-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93108034-G-C

96238031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93107791-C-T

96238301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93107558-T-C

96238578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93107377-C-T

96238580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93107375-C-T

http://identifiers.org/hco/12/GRCh38#96238860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93107122-C-A

96239012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93106979-A-G

96239216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93106774-A-G

96239479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93106494-G-A

96239649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93106370-T-C

96239847-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93106194-G-C

96239931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93106110-G-A

96239968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93106066-A-G

96240028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93106011-T-C

96240140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93105900-T-C

96240281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93105740-G-A

96240337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93105689-G-T

96240351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93105673-A-G

96240889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93105251-C-T

96240917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93105223-A-G

96244696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93103778-A-G

96244737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93103748-G-A

96244738-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93103747-C-G

96244941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93103542-G-A

96244941-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93103542-G-C

96244951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93103529-G-A

96245036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93103450-C-T

96245405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93103076-T-C

http://identifiers.org/hco/12/GRCh38#96245725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93102791-C-A

96245725-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93102791-C-G

96245725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93102791-C-T

96246803-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93101707-C-G

96246803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93101707-C-T

96246847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93101663-G-A

96246847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93101663-G-T

96247030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 93101450-A-G

96247030-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 93101450-A-T

96247114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 93101366-G-A

96247114-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 93101366-G-C

96247114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 93101366-G-T

96247126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 93101354-A-G

96247126-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 93101354-A-T

http://identifiers.org/hco/12/GRCh38#96247192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93101288-C-A

96247192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 93101288-C-T

96247321-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93101159-C-G

96247325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93101155-T-C

96247427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93101047-G-A

96247438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93101036-G-A

http://identifiers.org/hco/12/GRCh38#96247715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93100759-C-A

96247715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 93100759-C-T

96247735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 93100739-G-T

96247739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93100735-G-A

96247739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93100735-G-T

96247748-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93100726-C-G

96247748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93100726-C-T

96247749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93100725-T-C

96247795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93100701-G-T

96247853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93100653-G-A

96247853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93100653-G-T

96247859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93100647-T-C

96247859-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93100647-T-G

96248445-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93100188-C-G

96248621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93100062-G-A

96249112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93099777-T-C

96249115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93099774-A-G

96249231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93099655-G-A

96249231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93099655-G-T

96249245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93099639-G-A

96249245-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93099639-G-C

96249376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93099509-C-T

96249433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93099453-C-T

96249434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93099452-G-A

http://identifiers.org/hco/12/GRCh38#96249761-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93099155-A-C

96249761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93099155-A-G

96253694-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93096530-T-G

96253885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93096329-T-C

96253924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93096291-T-C

96253926-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93096289-C-G

96253926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93096289-C-T

96254099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93096174-C-T

96254109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93096164-G-A

96254612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93095875-A-G

96254889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93095645-G-A

96255000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93095538-T-C

96255137-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93095398-G-C

96255157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93095378-T-C

http://identifiers.org/hco/12/GRCh38#96255200-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#93095345-A-C

96255410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93095079-T-C

http://identifiers.org/hco/12/GRCh38#96255464-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93095009-A-C

96255464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93095009-A-G

96255480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93094998-T-C

96255503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93094982-G-A

96255503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93094982-G-T

http://identifiers.org/hco/12/GRCh38#96256724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93093238-C-A

96256750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93093207-T-C

96256754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93093203-G-A

96256796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93093163-T-C

96257254-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93092775-C-G

http://identifiers.org/hco/12/GRCh38#96257444-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93092592-A-C

96257444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93092592-A-G

96257471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93092564-C-T

96257745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93092359-C-T

96258057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93091987-C-T

96258205-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93091840-T-G

96258296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93091744-C-T

96258427-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93091611-G-C

96258863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93091228-G-T

96258891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93091200-G-A

http://identifiers.org/hco/12/GRCh38#96258939-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93091152-A-C

96258939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93091152-A-G

96259167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93090893-A-G

http://identifiers.org/hco/12/GRCh38#96259658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93090742-C-A

http://identifiers.org/hco/12/GRCh38#96259800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93090602-C-A

96259800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 93090602-C-T

http://identifiers.org/hco/12/GRCh38#96259818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93090584-C-A

96259818-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 93090584-C-G

96259818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 93090584-C-T

96259880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93090522-A-G

http://identifiers.org/hco/12/GRCh38#96259886-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93090516-A-C

96259886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93090516-A-G

96259893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93090509-G-T

96259895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93090507-G-A

96259895-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93090507-G-C

96259895-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93090507-G-T

http://identifiers.org/hco/12/GRCh38#96259927-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93090469-A-C

96259976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93090422-G-A

96259976-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93090422-G-C

96259976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93090422-G-T

96260047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93090346-T-C

96260397-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93090154-G-C

96260555-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93089870-T-A

96260696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93089734-G-A

96260755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93089688-C-T

http://identifiers.org/hco/12/GRCh38#96261125-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93089347-A-C

96261181-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93089289-G-C

96261211-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93089256-T-G

96261544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93089049-G-T

96261546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93089047-A-G

96261572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93089032-T-C

96261581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93089024-A-G

96261663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93088944-T-C

96261682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93088925-T-C

96261682-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93088925-T-G

96261805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93088832-T-C

http://identifiers.org/hco/12/GRCh38#96261960-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93088708-A-C

96261971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93088700-C-T

96262613-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93088360-A-T

96265992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93087138-A-G

96265998-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93087132-G-C

96266252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93086891-G-T

96266253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93086890-C-T

96266410-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93086692-T-G

96266445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93086669-G-A

96266518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93086597-T-C

96266952-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93086090-T-A

96266952-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93086090-T-G

96267007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93086030-A-G

96267010-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93086027-G-T

96267071-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93085979-G-C

96267158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 93085892-C-T

96267211-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 93085820-A-T

96267348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 93085677-T-C

http://identifiers.org/hco/12/GRCh38#96267549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93085457-C-A

96267558-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93085448-G-C

96267581-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93085420-T-A

96267581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93085420-T-C

96267609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93085396-G-T

96267624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93085381-G-A

96267624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93085381-G-T

96267711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93085319-G-A

96267711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93085319-G-T

96267940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93085092-T-C

96268247-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93084668-A-T

96268370-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93084552-A-T

96268386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93084537-A-G

http://identifiers.org/hco/12/GRCh38#96268434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93084492-C-A

96268472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93084451-T-C

96268570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93084378-A-G

96268750-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93084199-A-T

96268796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93084156-T-C

96268823-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93084132-G-C

96268823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93084132-G-T

96268965-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93084021-T-A

96268994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93083991-G-A

http://identifiers.org/hco/12/GRCh38#96269038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93083951-C-A

96269074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93083915-A-G

96269083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93083906-C-T

96269319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3325
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 93083721-G-T