33323746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128646540-C-T

33323959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128646345-G-A

33323959-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128646345-G-T

33323972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128646330-A-G

33324019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128646288-C-T

33324020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128646287-T-C

33324020-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128646287-T-G

33324029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128646282-T-C

33324065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128646250-G-T

33324185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128646137-A-G

33324366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128645962-G-T

33324378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128645950-C-T

http://identifiers.org/hco/1/GRCh38#33324392-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128645937-A-C

33324415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128645914-G-T

33324440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128645890-G-A

http://identifiers.org/hco/1/GRCh38#33324463-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128645869-A-C

33324463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128645869-A-G

33324596-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128645735-G-C

33324596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128645735-G-T

http://identifiers.org/hco/1/GRCh38#33324683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128645650-C-A

33324683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128645650-C-T

33324765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128645573-C-T

33325033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128645284-A-G

33325187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128645185-G-A

33325187-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128645185-G-C

33325822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128644731-G-A

33325841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128644712-G-A

33325890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128644669-G-A

33325890-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128644669-G-C

33325936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128644631-G-A

33326007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128644577-G-A

33326007-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128644577-G-T

33326180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128644422-G-T

http://identifiers.org/hco/1/GRCh38#33326800-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128643918-A-C

33327249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128643383-T-C

33327634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128642885-A-G

33328222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128642382-C-T

33328297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128642322-G-A

33328803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128642138-T-C

33328840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128642100-G-A

33328840-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128642100-G-C

33328840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128642100-G-T

33328971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 128641974-A-G

33329004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 128641941-C-T

33329010-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 128641935-C-G

33329010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 128641935-C-T

33329097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 128641848-T-C

33329216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128641726-G-A

33329216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128641726-G-T

33329242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128641707-A-G

33329242-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128641707-A-T

33329283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128641683-A-G

33329283-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128641683-A-T

http://identifiers.org/hco/1/GRCh38#33329697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128641317-C-A

33329919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128641138-G-A

33329919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128641138-G-T

33329934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128641123-G-A

33329934-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128641123-G-C

33329934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128641123-G-T

33329965-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128641101-G-T

33329971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128641095-G-A

33329971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128641095-G-T

33330037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128641058-G-A

33330037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128641058-G-T

33330356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128640780-G-T

33330414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128640733-G-A

33330681-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128640467-C-G

33330763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128640415-A-G

33330887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128640282-G-A

33331065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128639981-A-G

33331126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128639942-G-A

33331191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128639872-T-C

33331272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128639783-G-A

33331272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128639783-G-T

33331496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128639551-G-T

33331509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128639538-A-G

33331630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128639410-G-A

33331630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128639410-G-T

33331649-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128639394-T-G

http://identifiers.org/hco/1/GRCh38#33331706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128639364-C-A

http://identifiers.org/hco/1/GRCh38#33331764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128639302-C-A

33332218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128638982-G-A

33332218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128638982-G-T

33332236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128638964-C-T

http://identifiers.org/hco/1/GRCh38#33332564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#128638636-C-A

33332564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128638636-C-T

33332782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128638446-G-A

33332897-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128638346-A-T

33333047-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128638205-G-C

33333055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128638197-A-G

33333254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128638006-T-C

33333397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128637904-T-C

33333724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128637708-G-A

33333732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128637700-C-T

33333929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128637511-A-G

33333929-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128637511-A-T

33334290-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 128637147-T-A

33334307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128637121-G-A

33334307-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128637121-G-C

33334317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128637111-A-G

http://identifiers.org/hco/1/GRCh38#33334400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128637025-C-A

33334400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128637025-C-T

33334668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128636783-G-T

33334894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128636588-G-T

http://identifiers.org/hco/1/GRCh38#33335022-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128636474-A-C

33335022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128636474-A-G

http://identifiers.org/hco/1/GRCh38#33335045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128636452-C-A

33335160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128636359-A-G

33336965-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128632707-A-T

33337271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128632399-A-G

33337329-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128632346-C-G

33337329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128632346-C-T

33337469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128632219-A-G

33338147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128631691-A-G

33338317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128631485-G-A

33338317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128631485-G-T

33338583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128631225-T-C

33338873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128630924-G-A

33338873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128630924-G-T

33339180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128630696-C-T

33339641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128630294-T-C

33340612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128629796-C-T

33340863-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128629619-T-G

33340866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128629616-G-A

http://identifiers.org/hco/1/GRCh38#33341001-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128629565-A-C

33341509-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128629054-C-G

33341562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128628992-C-T

33341872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128628692-G-T

33342064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128628539-T-C

33342264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128628361-G-A

33342366-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128628254-G-C

http://identifiers.org/hco/1/GRCh38#33342511-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#128628126-A-C

http://identifiers.org/hco/1/GRCh38#33342530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#128628113-C-A

33342807-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128627841-G-C

33342949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128627737-G-A

33343803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128627388-C-T

33343804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128627387-G-A

33343875-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128627320-C-G

33343875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128627320-C-T

33343978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128627223-A-G

http://identifiers.org/hco/1/GRCh38#33344020-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128627177-A-C

33344096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128627106-C-T

33344147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128627049-T-C

33344471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128626747-T-C

http://identifiers.org/hco/1/GRCh38#33344598-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128626490-A-C

33344607-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128626481-T-A

33344638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128626433-C-T

http://identifiers.org/hco/1/GRCh38#33344740-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128626334-A-C

33344740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128626334-A-G

33344742-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128626332-C-G

33344798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128626266-G-A

http://identifiers.org/hco/1/GRCh38#33345002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128625986-C-A

http://identifiers.org/hco/1/GRCh38#33345035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128625953-C-A

33345076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128625913-G-A

33345086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128625903-T-C

33345111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128625877-G-A

33345111-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128625877-G-C

33345201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128625804-T-C

http://identifiers.org/hco/1/GRCh38#33345204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128625801-C-A

33345216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128625789-A-G

33345357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128625678-C-T

33345401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128625639-G-A

33345401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128625639-G-T

http://identifiers.org/hco/1/GRCh38#33345473-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128625568-C-A

33345492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128625557-T-C

33345496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128625553-A-G

33345560-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128625506-T-A

http://identifiers.org/hco/1/GRCh38#33345564-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128625502-A-C

33345596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128625474-G-A

33345674-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128624859-T-A

33345761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128624779-G-A

33345761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128624779-G-T

33345790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128624750-A-G

33345881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128624670-A-G

http://identifiers.org/hco/1/GRCh38#33345919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128624634-C-A

33345919-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128624634-C-G

33345919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128624634-C-T

33346365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128624312-T-C

33346544-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128624191-T-A

33346595-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128624147-C-G

33346595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128624147-C-T

33346596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128624146-G-A

33346596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128624146-G-T

33346598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128624144-A-G

33346818-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128624004-T-G

33346820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128624002-A-G

33346820-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128624002-A-T

http://identifiers.org/hco/1/GRCh38#33346827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128623995-C-A

33346903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128623901-G-T

33347018-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128623804-T-A

33347120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128623699-G-A

33347120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128623699-G-T

33347233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128623593-A-G

33347403-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128623452-T-A

33347403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128623452-T-C

33347424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128623435-T-C

33347574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128623236-A-G

33347581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128623229-G-T

33347687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128623132-A-G

33347823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128623001-G-A

33347823-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128623001-G-C

33347823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128623001-G-T

33347834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128622990-A-G

http://identifiers.org/hco/1/GRCh38#33347847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128622978-C-A

33347862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128622963-A-G

http://identifiers.org/hco/1/GRCh38#33347884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128622954-C-A

33347885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128622953-T-C

http://identifiers.org/hco/1/GRCh38#33347888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128622950-C-A

33347888-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128622950-C-G

33347903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128622935-A-G

33347964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128622884-T-C

http://identifiers.org/hco/1/GRCh38#33348179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128622725-C-A

http://identifiers.org/hco/1/GRCh38#33348199-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128622705-A-C

33348544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128622375-T-C

33348915-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128622044-C-G

33349361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 128621794-G-A

http://identifiers.org/hco/1/GRCh38#33349601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128621657-C-A

33349601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 128621657-C-T

33349615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 128621643-G-A

33349615-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 128621643-G-T

33349813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 128621467-G-A

33349858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 128621437-G-A

33349858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 128621437-G-T

http://identifiers.org/hco/1/GRCh38#33349859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#128621436-C-A

33349859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 128621436-C-T

33349871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 128621424-G-A

33349871-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 128621424-G-C

33349910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, undefined
orthologous variants: 128621386-G-T

33349933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128621364-G-A

33349933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128621364-G-T

33349968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, undefined
orthologous variants: 128621332-G-A

33350066-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128621242-G-C

http://identifiers.org/hco/1/GRCh38#33350251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128621126-C-A

33350251-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128621126-C-G

http://identifiers.org/hco/1/GRCh38#33350357-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#128621019-A-C

33350474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128620897-G-A

33350474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128620897-G-T

33350526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128620845-G-T

33350551-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128620820-C-G

33350551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128620820-C-T

33350561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128620811-G-T

33350807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128620594-T-C

33351124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128620294-C-T

33351272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128620165-T-C

33351272-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128620165-T-G

33351469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128620008-T-C

33351490-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128619987-C-G

33352036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128619760-T-C

33352160-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128619657-G-T

http://identifiers.org/hco/1/GRCh38#33352291-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128619478-A-C

33352429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128619345-G-A

33352994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128618818-C-T

33353050-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128618766-G-C

33353636-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128618179-C-G

33353793-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128618030-G-C

33353834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128617989-C-T

http://identifiers.org/hco/1/GRCh38#33354079-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128617778-C-A

33354235-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128617670-T-G

http://identifiers.org/hco/1/GRCh38#33354274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128617631-C-A

33354274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128617631-C-T

33354295-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128617597-T-A

33354296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128617596-G-A

33354296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128617596-G-T

http://identifiers.org/hco/1/GRCh38#33354345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128617549-C-A

http://identifiers.org/hco/1/GRCh38#33354360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128617534-C-A

33354360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128617534-C-T

33354412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128617493-G-A

http://identifiers.org/hco/1/GRCh38#33354579-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128617325-A-C

33354579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128617325-A-G

33354698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128617219-G-A

33354698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128617219-G-T

33354720-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128617198-T-G

33355313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128616649-C-T

http://identifiers.org/hco/1/GRCh38#33355323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128616639-C-A

33355323-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128616639-C-G

33355323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128616639-C-T

33356251-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128616374-A-T

http://identifiers.org/hco/1/GRCh38#33356263-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128616362-A-C

33356263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128616362-A-G

33357171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128615727-A-G

33357946-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128614997-G-C

33358004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128614937-A-G

33358250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128614149-A-G

33358438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128613975-A-G

33358484-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128613932-A-T

33358594-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128613822-T-A

33358798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128613629-T-C

33358897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128613620-A-G

33358964-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128613611-T-A

33359073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 128613528-A-G

33362676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128611482-G-T

33362683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128611475-G-A

33362683-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128611475-G-C

33362775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128611389-A-G

33362781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128611383-A-G

33362781-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128611383-A-T

33363007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128611146-A-G

33363193-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128610761-C-G

33363193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128610761-C-T

33363251-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128610689-T-A

33363251-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128610689-T-G

http://identifiers.org/hco/1/GRCh38#33363308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128610638-C-A

33363308-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128610638-C-G

33363391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128610529-T-C

33363602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128610304-G-A

33363642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128610265-G-T

33363786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128610116-G-A

33364611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128609357-G-T

33364754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128609215-A-G

33365133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128608836-C-T

33365269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128608721-A-G

33365571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128607736-G-A

33365656-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128607652-C-G

33365656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128607652-C-T

33365782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128607537-G-A

33366348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128606832-C-T

33366418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128606777-G-A

33366521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128606650-T-C

33366569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128606598-A-G

33366634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128606568-T-C

33366885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128606346-T-C

33366978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128606267-G-T

33366993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128606252-G-T

33367041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128606216-A-G

33367157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, missense_variant
orthologous variants: 128606109-C-T

33367162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 128606104-G-A

33367229-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, missense_variant
orthologous variants: 128606049-A-T

33367415-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, missense_variant
orthologous variants: 128605863-G-C

33367415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, missense_variant
orthologous variants: 128605863-G-T

http://identifiers.org/hco/1/GRCh38#33367467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128605809-C-A

33367467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128605809-C-T

33367499-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128605777-G-C

33367499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128605777-G-T

33367515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128605762-G-A

33367515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128605762-G-T

33367519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128605744-T-C

33367519-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128605744-T-G

33367520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128605743-G-A

33367520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128605743-G-T

33367558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128605685-G-T

33367559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128605674-A-G

33367559-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128605674-A-T

33367825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128605468-A-G

33367882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, undefined
orthologous variants: 128605425-G-T

http://identifiers.org/hco/1/GRCh38#33368392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128605045-C-A

33368392-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128605045-C-G

33368392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128605045-C-T

http://identifiers.org/hco/1/GRCh38#33368424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128605032-C-A

33368424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128605032-C-T

33368491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128604980-A-G

33368491-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128604980-A-T

http://identifiers.org/hco/1/GRCh38#33368640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128604831-C-A

33368640-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 128604831-C-G

33368640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 128604831-C-T

33368666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 128604806-T-C

33369066-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128604566-G-C

33369248-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128604375-T-G

33369284-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128604339-G-C

33369284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128604339-G-T

33369383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128604245-T-C

33369625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128604053-C-T

33369681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128603999-G-A

33370195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128603651-G-A

http://identifiers.org/hco/1/GRCh38#33370329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128603536-C-A

33370406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128603469-G-A

33370509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 128603366-C-T

33370597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128603278-G-A

http://identifiers.org/hco/1/GRCh38#33370650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128603213-C-A

33370713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128603150-G-A

33370713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128603150-G-T

33370772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128603091-G-A

33370871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128602999-T-C

http://identifiers.org/hco/1/GRCh38#33370886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128602989-C-A

33370886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128602989-C-T

http://identifiers.org/hco/1/GRCh38#33370940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128602935-C-A

33370965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128602908-C-T

33371148-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128602718-C-G

33371148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128602718-C-T

33371166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128602702-C-T

33371200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128602684-G-A

33371200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128602684-G-T

http://identifiers.org/hco/1/GRCh38#33371202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128602681-C-A

33371202-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128602681-C-G

33371202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128602681-C-T

33371203-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128602680-T-A

33371223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128602663-C-T

http://identifiers.org/hco/1/GRCh38#33371244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128602650-C-A

33371245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128602649-A-G

33371416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128602555-C-T

33371488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128602518-C-T

33371489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128602517-C-T

33371678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128602378-G-A

http://identifiers.org/hco/1/GRCh38#33372155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128602004-C-A

33372155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128602004-C-T

33372193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128601982-G-A

33372193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128601982-G-T

33372222-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128601959-T-A

http://identifiers.org/hco/1/GRCh38#33372243-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128601934-A-C

33372243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128601934-A-G

33372244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128601933-A-G

33372275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128601902-T-C

http://identifiers.org/hco/1/GRCh38#33372279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128601898-C-A

33372279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128601898-C-T

33372320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 128601855-G-A

33372404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 128601771-T-C

33372404-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 128601771-T-G

33372487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128601691-G-A

33372487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128601691-G-T

33372535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128601675-T-C

http://identifiers.org/hco/1/GRCh38#33372536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128601674-C-A

33372536-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128601674-C-G

33372536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128601674-C-T

33372549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128601661-G-T

33372620-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128601645-G-C

33372624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128601641-G-A

33372812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128601496-A-G

http://identifiers.org/hco/1/GRCh38#33374010-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128600965-A-C

33374033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128600958-C-T

33374146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128600828-G-A

http://identifiers.org/hco/1/GRCh38#33375242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128599143-C-A

33375242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128599143-C-T

33375320-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128599067-T-G

33375433-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 128598949-C-G

33375435-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 128598947-A-T

33375441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 128598941-G-A

33375475-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 128598907-C-G

33375604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128598778-A-G

33375642-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128598741-G-C

33375642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128598741-G-T

33375663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128598721-T-C

http://identifiers.org/hco/1/GRCh38#33375680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128598704-C-A

33375680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128598704-C-T

33376017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128598400-G-A

33376285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128598289-T-C

33376292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128598282-T-C

33376641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128597972-A-G

33376965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128597630-C-T

33377154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128597333-C-T

33377269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128597229-C-T

33377335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128597142-A-G

33377505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128596802-G-A

33377604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128596662-C-T

33377811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128596478-G-T

33378081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128595976-C-T

33378364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128595410-A-G

33378365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128595409-A-G

33379753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128594752-T-C

33379862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128594655-C-T

http://identifiers.org/hco/1/GRCh38#33380027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128594540-C-A

33380273-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128594316-A-T

33380628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128593910-T-C

33380715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128593866-T-C

33380875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128593724-C-T

33380893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128593706-T-C

33380988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128593623-G-A

33381044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128593568-G-A

33381131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128593495-G-A

33381442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128593249-A-G

33381553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128593135-G-T

33381614-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128592942-C-G

33381735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128592871-C-T

33381765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128592841-A-G

33382152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128592519-A-G

33382296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128592380-T-C

33382314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128592358-T-C

33382534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128592151-A-G

http://identifiers.org/hco/1/GRCh38#33383201-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128591513-A-C

33383201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128591513-A-G

33383217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128591497-G-A

33383525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128590808-G-T

33383543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128590790-G-A

33383622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128590727-A-G

33383684-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128590673-T-A

33383684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128590673-T-C

33383813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128590616-G-A

33384017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128590498-G-A

http://identifiers.org/hco/1/GRCh38#33384391-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128590143-A-C

33384893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128589497-G-A

33384900-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128589490-G-C

33385164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128589236-T-C

33385297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128589099-C-T

33387089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128587872-T-C

33387176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128587788-G-A

33387471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128587540-A-G

http://identifiers.org/hco/1/GRCh38#33387486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128587520-C-A

http://identifiers.org/hco/1/GRCh38#33387544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128587465-C-A

http://identifiers.org/hco/1/GRCh38#33387668-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128587352-A-C

33387865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128587183-G-A

33388355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128586818-C-T

33388785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128586598-G-A

33388785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128586598-G-T

33388812-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128586570-T-G

33388822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128586560-A-G

33389076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128586327-G-A

33389076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128586327-G-T

33389098-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128586299-T-A

33389098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128586299-T-C

33389155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128586223-G-T

33389197-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128586161-G-C

33389498-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128585887-T-A

33389611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128585371-G-A

33389614-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128585368-C-G

33389614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128585368-C-T

33389665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128585317-T-C

33389677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128585305-T-C

33389805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128585230-C-T

33389877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128585161-T-C

33390122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128584956-C-T

33390123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128584955-G-A

33390181-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128584915-T-G

33390195-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128584898-T-G

33390726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128584388-G-T

http://identifiers.org/hco/1/GRCh38#33390784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128584330-C-A

33391142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128584056-T-C

33391401-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128583920-C-G

http://identifiers.org/hco/1/GRCh38#33391599-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128583748-A-C

http://identifiers.org/hco/1/GRCh38#33391637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128583711-C-A

33391774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128583587-G-A

33392171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128583218-A-G

33392188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128583199-C-T

33392222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128583164-A-G

33392335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128583027-C-T

33392534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128582834-G-A

33392594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128582778-T-C

33392619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128582699-A-G

33392767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 128582553-T-C

http://identifiers.org/hco/1/GRCh38#33393051-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128582265-A-C

33393052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128582264-T-C

33393251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128582090-C-T

33393902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128582018-G-A

33394191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128581805-T-C

33395623-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128578737-G-C

33395676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128578684-G-A

33395701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128578659-T-C

33395772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128578590-A-G

http://identifiers.org/hco/1/GRCh38#33395786-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128578576-A-C

http://identifiers.org/hco/1/GRCh38#33395815-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128578546-A-C

33395989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128578391-T-C

33396297-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128578121-C-G

33396354-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128578066-A-T

33396712-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, undefined
orthologous variants: 128577729-G-C

33396864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128577613-C-T

33397183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, undefined
orthologous variants: 128577310-A-G

33399361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128576287-C-T

33399469-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128576199-G-C

33399480-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128576179-T-G

http://identifiers.org/hco/1/GRCh38#33399492-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128576167-A-C

33399518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128576130-T-C

33399533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128576116-T-C

33399603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128576038-C-T

33399604-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128576037-A-T

http://identifiers.org/hco/1/GRCh38#33399658-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128575986-A-C

33399723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128575934-G-A

33399822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128575841-G-A

33399954-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128575707-T-G

33400042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128575618-A-G

33400044-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128575616-T-A

33400044-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128575616-T-G

33400114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128575546-T-C

33400204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128575470-A-G

33404523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128573651-T-C

33409380-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128573578-G-C

33409664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128573334-G-T

33409885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128573129-A-G

33409900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128573115-A-G

http://identifiers.org/hco/1/GRCh38#33409943-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128573073-A-C

http://identifiers.org/hco/1/GRCh38#33409974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128573041-C-A

33410043-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128572977-G-C

33410218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128572813-C-T

http://identifiers.org/hco/1/GRCh38#33410440-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128572600-A-C

33410861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128572194-A-G

33410884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128572171-A-G

33411155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128571390-T-C

33411272-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128571275-C-G

33411272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128571275-C-T

33411485-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128571094-A-T

33411829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128570845-G-T

33412086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128570628-T-C

33412425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128569401-C-T

33413740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128566726-G-A

33413904-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128566562-C-G

33414365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128566119-G-T

33414415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128566060-A-G

33414864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128565581-A-G

33419988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128561572-T-C

33420982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128560736-C-T

33421007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128560710-G-A

33421088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128560650-C-T

33421097-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128560641-T-A

33421172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128560560-T-C

33421332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128560408-G-A

33421403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128560362-A-G

33422653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128559605-A-G

http://identifiers.org/hco/1/GRCh38#33422728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128559577-C-A

http://identifiers.org/hco/1/GRCh38#33423669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128558273-C-A

http://identifiers.org/hco/1/GRCh38#33423789-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128558197-A-C

33423789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128558197-A-G

http://identifiers.org/hco/1/GRCh38#33423933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128558092-C-A

33424177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128557920-T-C

33424309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron_variant, undefined
orthologous variants: 128557771-A-G

33424406-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128557684-A-T

33425019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128556253-G-A

33425498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128555915-C-T

33425773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128555573-G-A

33425879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128555461-G-A

33426065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128555291-G-A

33426067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128555289-G-A

33426383-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128555014-G-C

33426701-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128554733-A-T

33426716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128554718-G-T

33426729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128554706-G-A

33426777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128554649-C-T

33426789-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128554608-A-T

33428261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128551486-A-G

http://identifiers.org/hco/1/GRCh38#33428266-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128551481-A-C

33428328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128551428-T-C

33428353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128551403-A-G

33428395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128551365-C-T

33428676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128550775-A-G

33428771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128550680-A-G

http://identifiers.org/hco/1/GRCh38#33428812-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128550639-A-C

33428933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128550497-G-A

33429007-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128550390-T-G

33429712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128549727-C-T

33429994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128549463-G-A

33430010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: intron variant
orthologous variants: 128549448-T-C

33430358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 128549113-T-C

33430627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3183
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 128548850-T-C