93306432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37887683-A-G

93306543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37887794-T-C

93306620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37887867-G-T

http://identifiers.org/hco/10/GRCh38#93306646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37887891-C-A

93306646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37887891-C-T

http://identifiers.org/hco/10/GRCh38#93306751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37887992-C-A

93306751-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37887992-C-G

93306751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37887992-C-T

93306833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37888073-G-A

93306901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37888123-G-A

93306901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 37888123-G-T

93309061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37888669-G-T

93309129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37888737-T-C

http://identifiers.org/hco/10/GRCh38#93309901-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37889618-C-A

93309909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37889627-T-C

http://identifiers.org/hco/10/GRCh38#93309931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37889640-C-A

93309931-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37889640-C-G

http://identifiers.org/hco/10/GRCh38#93309943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37889652-C-A

http://identifiers.org/hco/10/GRCh38#93309955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37889666-C-A

93309955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37889666-C-T

93310016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37889681-C-T

93310230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37889887-G-T

93310250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37889904-T-C

93310304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37890028-A-G

93310304-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37890028-A-T

http://identifiers.org/hco/10/GRCh38#93310488-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37890214-A-C

93310611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 37890349-G-A

93310625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 37890363-A-G

93310871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37890609-T-C

93310899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37890636-C-T

93311170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37890852-G-A

http://identifiers.org/hco/10/GRCh38#93311193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37890874-C-A

93311699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37891210-C-T

93311807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37891315-A-G

93311828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37891330-A-G

93312827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37892027-G-A

93312927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37892059-C-T

93312956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37892088-A-G

93313034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 37892139-C-T

93313056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 37892161-T-C

93313134-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 37892239-C-G

93313134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 37892239-C-T

93313345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37892449-G-A

93316575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37893608-G-A

93316575-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37893608-G-C

93316575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37893608-G-T

93316638-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37893649-T-G

93316676-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37893691-C-G

93316676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37893691-C-T

93316745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 37893757-G-T

93316871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37893889-A-G

http://identifiers.org/hco/10/GRCh38#93316914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37893922-C-A

93316914-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37893922-C-G

93316914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37893922-C-T

http://identifiers.org/hco/10/GRCh38#93316916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37893924-C-A

93316916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37893924-C-T

http://identifiers.org/hco/10/GRCh38#93317215-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37894199-A-C

93317215-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37894199-A-T

93317326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37894301-G-T

http://identifiers.org/hco/10/GRCh38#93317543-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37894327-A-C

93317543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37894327-A-G

93317762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37894427-T-C

93317957-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37894608-C-G

93318912-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37895021-G-C

93318917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37895026-C-T

93318993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37895075-C-T

http://identifiers.org/hco/10/GRCh38#93319073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37895195-C-A

93319130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37895258-T-C

93319398-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37895551-T-G

http://identifiers.org/hco/10/GRCh38#93319477-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37895630-A-C

93319527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37895686-T-C

93319588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37895746-T-C

93319767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37895931-G-A

93319767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37895931-G-T

93319839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37896002-A-G

http://identifiers.org/hco/10/GRCh38#93320081-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37896244-A-C

93320081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37896244-A-G

93320170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37896343-G-A

http://identifiers.org/hco/10/GRCh38#93320194-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37896367-A-C

93320223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37896396-C-T

93320665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37896844-T-C

93321930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37898181-G-A

93321943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37898194-C-T

http://identifiers.org/hco/10/GRCh38#93322143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37898379-C-A

93322513-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37898823-T-G

http://identifiers.org/hco/10/GRCh38#93322517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37898827-C-A

93322533-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37898845-G-C

93322910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37899184-C-T

93322923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37899194-G-A

http://identifiers.org/hco/10/GRCh38#93322970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37899235-C-A

http://identifiers.org/hco/10/GRCh38#93322978-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37899243-A-C

93323009-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37899274-A-T

93323022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37899287-G-A

93323022-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37899287-G-T

93323029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37899294-A-G

93323036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37899301-G-A

http://identifiers.org/hco/10/GRCh38#93323064-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37899328-C-A

93323064-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37899328-C-G

93323064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37899328-C-T

93323148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 37899412-T-C

93323202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37899475-T-C

93323219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37899492-C-T

93323235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37899511-G-A

93323287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 37899555-T-C

http://identifiers.org/hco/10/GRCh38#93323469-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37899781-A-C

93323488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 37899800-A-G

http://identifiers.org/hco/10/GRCh38#93323611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37899907-C-A

93323611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 37899907-C-T

http://identifiers.org/hco/10/GRCh38#93323650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37899946-C-A

http://identifiers.org/hco/10/GRCh38#93323742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37900026-C-A

http://identifiers.org/hco/10/GRCh38#93323743-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37900027-A-C

93323743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37900027-A-G

http://identifiers.org/hco/10/GRCh38#93323768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37900049-C-A

93323779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37900056-C-T

93324126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 37900402-C-T

93324372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 37900667-T-C

http://identifiers.org/hco/10/GRCh38#93324466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37900761-C-A

93324576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37900861-T-C

93324616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37900904-A-G

93324640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37900928-T-C

http://identifiers.org/hco/10/GRCh38#93324652-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37900940-A-C

93324652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37900940-A-G

93324849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37900975-G-A

93325217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37901178-A-G

93325239-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37901200-A-T

93325470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37901417-A-G

93325470-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37901417-A-T

93325688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37901660-A-G

93325726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37901698-C-T

93325760-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37901733-A-T

93325768-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37901741-T-A

93325768-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37901741-T-G

93325792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37901764-G-A

93325797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37901769-T-C

93325930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 37901889-G-A

93325930-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 37901889-G-C

93326294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37902267-G-T

93327016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37902619-G-A

93327239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37902833-T-C

93327258-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37902854-T-A

93327288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37902880-G-A

93327534-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37902988-T-G

http://identifiers.org/hco/10/GRCh38#93328292-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37903425-A-C

93328292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37903425-A-G

http://identifiers.org/hco/10/GRCh38#93328330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37903452-C-A

93328330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37903452-C-T

http://identifiers.org/hco/10/GRCh38#93328331-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37903453-C-A

93328487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37903768-T-C

http://identifiers.org/hco/10/GRCh38#93328573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37903855-C-A

93328582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37903870-G-A

93328612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37903903-G-A

93328612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37903903-G-T

http://identifiers.org/hco/10/GRCh38#93328617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37903908-C-A

93328618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37903909-T-C

93328741-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37904031-C-G

93328741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37904031-C-T

93328788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 37904079-T-C

93328812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 37904103-A-G

93328892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 37904183-G-A

93328892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 37904183-G-T

93328896-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 37904187-G-C

93328920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37904211-A-G

93328920-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37904211-A-T

93328924-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37904215-T-A

93328924-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37904215-T-G

http://identifiers.org/hco/10/GRCh38#93328971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37904232-C-A

93328971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37904232-C-T

http://identifiers.org/hco/10/GRCh38#93328985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37904246-C-A

93328985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37904246-C-T

http://identifiers.org/hco/10/GRCh38#93328986-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37904247-A-C

93328986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37904247-A-G

93328986-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37904247-A-T

http://identifiers.org/hco/10/GRCh38#93328991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37904251-C-A

93328991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37904251-C-T

93328995-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37904255-T-A

93329012-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37904271-T-A

93329012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37904271-T-C

93329050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37904304-T-C

http://identifiers.org/hco/10/GRCh38#93329297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37904554-C-A

93329297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37904554-C-T

93329552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37904737-T-C

93329552-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37904737-T-G

93329589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37904767-G-A

93329589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37904767-G-T

93329612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37904790-G-T

93329620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37904798-G-A

93329687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 37904864-G-A

93329687-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 37904864-G-C

93329687-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 37904864-G-T

93329768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 37904945-G-A

93329825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 37905002-T-C

93329880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37905057-T-C

93329928-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37905102-T-A

93329928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37905102-T-C

93329940-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37905111-T-A

http://identifiers.org/hco/10/GRCh38#93329950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37905121-C-A

http://identifiers.org/hco/10/GRCh38#93329955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37905127-C-A

93329955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37905127-C-T

93329979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37905145-T-C

93330640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37905926-G-A

93330789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37906099-C-T

93331141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37906809-C-T

93331249-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37906951-G-C

93331290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37906992-T-C

http://identifiers.org/hco/10/GRCh38#93331336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37907002-C-A

93331549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37907217-G-A

93331555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37907223-C-T

93331687-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37907356-T-G

http://identifiers.org/hco/10/GRCh38#93331703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37907370-C-A

93331703-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37907370-C-G

93331703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37907370-C-T

93331720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37907475-G-A

93331720-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37907475-G-C

93331720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37907475-G-T

93331728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37907509-G-A

93331774-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37907558-T-G

93331786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37907571-C-T

93331790-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37907575-C-G

93331812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37907594-A-G

93331813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37907595-T-C

93331815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37907597-T-C

93331896-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37907681-C-G

http://identifiers.org/hco/10/GRCh38#93332019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37908335-C-A

93332059-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37908374-C-G

93332059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37908374-C-T

93332060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37908375-C-T

93332200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37908513-G-A

93333097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37909080-G-A

93333097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37909080-G-T

93333103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37909086-T-C

93333132-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37909110-C-G

93333132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37909110-C-T

93333328-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37909275-G-C

93333328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37909275-G-T

http://identifiers.org/hco/10/GRCh38#93333406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37909348-C-A

http://identifiers.org/hco/10/GRCh38#93333450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37909394-C-A

93333450-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37909394-C-G

93333550-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37909558-T-A

93333573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37909581-T-C

http://identifiers.org/hco/10/GRCh38#93333578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37909593-C-A

93333785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 37909811-C-T

93333877-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 37909903-T-A

93333938-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37909973-C-G

http://identifiers.org/hco/10/GRCh38#93333945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37909980-C-A

93333945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37909980-C-T

http://identifiers.org/hco/10/GRCh38#93333955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37909987-C-A

93333955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37909987-C-T

93333993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37910037-A-G

93334026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37910069-T-C

93334045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37910081-A-G

93334893-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37910609-T-A

93335132-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37910821-C-G

http://identifiers.org/hco/10/GRCh38#93335422-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37911085-A-C

93335478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37911143-T-C

93335905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37911390-C-T

93335906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37911391-A-G

http://identifiers.org/hco/10/GRCh38#93335960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37911445-C-A

93335960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 37911445-C-T

93336017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 37911502-T-C

93336061-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37911546-C-G

93336061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37911546-C-T

93336065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37911550-G-A

93336192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37911655-A-G

93336227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37911687-A-G

93336289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37911743-G-A

93336434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37911940-G-A

93336434-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37911940-G-C

93336452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37911960-G-A

93336605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37912113-C-T

93336654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37912162-T-C

93336674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37912181-C-T

93337041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37912316-A-G

93337171-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37912431-A-T

http://identifiers.org/hco/10/GRCh38#93337297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37912547-C-A

93337309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37912564-G-A

http://identifiers.org/hco/10/GRCh38#93337402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37912651-C-A

http://identifiers.org/hco/10/GRCh38#93337561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37912815-C-A

93337561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 37912815-C-T

93337620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 37912874-T-C

93337695-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 37912947-T-G

http://identifiers.org/hco/10/GRCh38#93337720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37912972-C-A

93337720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 37912972-C-T

93337726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 37912977-A-G

93337990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37913236-T-C

93337994-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37913240-T-A

93338004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37913253-T-C

93338004-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37913253-T-G

http://identifiers.org/hco/10/GRCh38#93338017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37913259-C-A

93338017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37913259-C-T

93338315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37913899-T-C

93338356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37913929-A-G

http://identifiers.org/hco/10/GRCh38#93338381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37913948-C-A

93338567-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37914067-G-C

93338694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37914198-G-T

93338725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37914229-G-A

93339399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37915210-G-A

93340131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37915409-G-A

93340148-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37915426-G-C

http://identifiers.org/hco/10/GRCh38#93340388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37915657-C-A

93340402-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37915662-C-G

93340491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37915717-A-G

93340539-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37915768-C-G

93340643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37915869-T-C

93340662-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37915896-C-G

93340704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37915938-C-T

93340963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37916158-T-C

93341052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37916237-G-A

93341294-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37916429-A-T

93341637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37916527-T-C

http://identifiers.org/hco/10/GRCh38#93341883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37916773-C-A

93341883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37916773-C-T

93341958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 37916847-A-G

93342016-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37916905-T-A

93342016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37916905-T-C

93342073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37916962-G-T

93342094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37916983-G-T

93342167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37917035-A-G

93342222-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37917084-C-G

93342222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37917084-C-T

93342336-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37917197-C-G

93342337-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37917198-T-G

93342546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37917402-A-G

93342657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37917489-C-T

93342687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37917507-T-C

93342709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37917529-T-C

93342979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37917793-C-T

93343013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37917827-C-T

93343184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37917999-G-A

93343219-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37918029-C-G

93343263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37918068-T-C

93343705-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37919323-A-T

93343793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37919408-G-T

93343982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37919560-G-A

http://identifiers.org/hco/10/GRCh38#93344026-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37919604-A-C

93344027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37919605-T-C

93344043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37919619-T-C

93344072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37919645-A-G

93344101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37919674-T-C

http://identifiers.org/hco/10/GRCh38#93344835-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37920269-A-C

93346879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37920650-T-C

93346880-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37920651-G-C

93346938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37920704-G-T

93347039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37920806-G-A

93347039-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37920806-G-C

93347082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37920850-C-T

93347096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37920864-C-T

93347134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37920902-G-A

93347571-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37921012-A-T

http://identifiers.org/hco/10/GRCh38#93347593-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37921034-C-A

93347606-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37921047-T-A

93347665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 37921099-G-A

93347665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 37921099-G-T

93347729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 37921163-G-A

93347729-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 37921163-G-C

93347801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37921235-G-T

http://identifiers.org/hco/10/GRCh38#93347814-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37921253-A-C

http://identifiers.org/hco/10/GRCh38#93347848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37921289-C-A

93347852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37921293-A-G

http://identifiers.org/hco/10/GRCh38#93347858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37921299-C-A

93347858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37921299-C-T

http://identifiers.org/hco/10/GRCh38#93347863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37921304-C-A

93347883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37921330-G-A

93347883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37921330-G-T

93347902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37921354-G-A

93347927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37921379-G-A

93347927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37921379-G-T

93347946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37921397-C-T

93347947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37921398-G-A

93348208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37921657-C-T

93348269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37921796-A-G

93348365-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37921899-C-G

93348365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37921899-C-T

93348566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37922084-G-A

93348635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37922167-G-A

93348709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37922219-C-T

http://identifiers.org/hco/10/GRCh38#93348792-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37922293-A-C

93348792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37922293-A-G

93348834-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37922305-G-T

93349002-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37922448-C-G

93349002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37922448-C-T

93349032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37922478-G-A

93349177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37922744-T-C

93349211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37922778-C-T

93349262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37922821-C-T

93349266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37922825-T-C

93349455-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37922988-C-G

93349778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37923178-A-G

93349913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 37923313-G-A

http://identifiers.org/hco/10/GRCh38#93350010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37923410-C-A

http://identifiers.org/hco/10/GRCh38#93350018-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37923418-A-C

93350084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37923600-A-G

93350110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37923625-A-G

93350225-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37923676-C-G

93350690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37923835-C-T

93350691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37923849-A-G

93350894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37924037-C-T

http://identifiers.org/hco/10/GRCh38#93351060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37924166-C-A

93351060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37924166-C-T

93351114-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37924220-G-C

http://identifiers.org/hco/10/GRCh38#93351154-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37924251-A-C

93351183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37924280-G-A

93351239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 37924337-G-T

http://identifiers.org/hco/10/GRCh38#93351324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37924421-C-A

93351324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37924421-C-T

93351359-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37924456-A-T

93351622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37924718-C-T

http://identifiers.org/hco/10/GRCh38#93351929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37925025-C-A

http://identifiers.org/hco/10/GRCh38#93351961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37925057-C-A

93351961-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37925057-C-G

93351961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37925057-C-T

93352039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37925129-C-T

93352183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37925256-C-T

93352208-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37925276-G-C

93352382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37925451-T-C

93352803-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37925722-T-G

93352966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37925919-A-G

93353606-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37926101-T-G

93353701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37926196-A-G

93353711-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37926206-T-A

93353711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37926206-T-C

93353711-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37926206-T-G

93353726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37926220-A-G

http://identifiers.org/hco/10/GRCh38#93353751-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37926256-A-C

93353751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37926256-A-G

93353751-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37926256-A-T

93353978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37926466-G-T

93353979-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37926467-A-T

93353980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37926468-T-C

93353980-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37926468-T-G

http://identifiers.org/hco/10/GRCh38#93354014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37926496-C-A

93354014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37926496-C-T

93354016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37926498-G-A

93354016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37926498-G-T

93354021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37926503-G-A

93354028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37926510-T-C

93354028-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37926510-T-G

93354533-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37927342-G-C

http://identifiers.org/hco/10/GRCh38#93355710-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37927830-A-C

93356373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37927971-C-T

93356443-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37928039-A-T

93356571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37928189-T-C

93356578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37928196-G-T

93356613-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37928231-T-G

93356678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 37928296-G-A

93356759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 37928377-G-T

http://identifiers.org/hco/10/GRCh38#93356798-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37928416-A-C

93356798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 37928416-A-G

93356804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 37928422-A-G

http://identifiers.org/hco/10/GRCh38#93356898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37928508-C-A

http://identifiers.org/hco/10/GRCh38#93356953-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37928563-A-C

93356953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37928563-A-G

93356987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37928598-G-A

93357039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37928650-A-G

http://identifiers.org/hco/10/GRCh38#93357265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37928818-C-A

93357265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37928818-C-T

93357366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37928920-G-A

93357578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37929149-A-G

93357608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37929179-T-C

93357609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37929180-A-G

93359472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37930344-C-T

93359690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37930531-G-A

93359690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37930531-G-T

93359744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37930577-A-G

93359744-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37930577-A-T

93359751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37930583-G-T

93359759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37930591-G-A

93359759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37930591-G-T

93359802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37930635-C-T

93359813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37930646-C-T

93359839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 37930672-G-A

93359852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 37930685-G-A

93359852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 37930685-G-T

93359887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 37930720-C-T

93360079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37930917-G-A

93360079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37930917-G-T

93360088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37930926-T-C

93360088-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37930926-T-G

93360366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37931194-T-C

93360800-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37931583-G-C

93360849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37931630-C-T

93361360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37931802-A-G

http://identifiers.org/hco/10/GRCh38#93361403-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37931845-C-A

93361543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 37931982-T-C

93361560-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 37931999-T-A

93361560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 37931999-T-C

http://identifiers.org/hco/10/GRCh38#93361676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37932106-C-A

93362821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37932677-T-C

93362821-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37932677-T-G

http://identifiers.org/hco/10/GRCh38#93362845-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37932701-A-C

93362852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37932715-A-G

93362898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37932753-T-C

93362963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37932819-A-G

93363012-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37932871-C-G

93363821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37933963-A-G

93363821-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37933963-A-T

93363861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37934003-G-A

93363861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37934003-G-T

93363873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37934015-A-G

93363873-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37934015-A-T

93363922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37934042-G-A

93363922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37934042-G-T

http://identifiers.org/hco/10/GRCh38#93363953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37934071-C-A

93363970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 37934088-G-A

http://identifiers.org/hco/10/GRCh38#93364057-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37934175-A-C

93364318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37934443-G-T

93364551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37934696-C-T

http://identifiers.org/hco/10/GRCh38#93364852-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37934948-A-C

93365197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37935272-T-C

93365469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37935712-A-G

http://identifiers.org/hco/10/GRCh38#93365545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37935778-C-A

93365545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37935778-C-T

93365748-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37935955-T-A

93365877-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37936096-T-G

93365915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37936134-T-C

93365973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37936190-C-T

93366265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37937438-G-T

93366796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37938427-C-T

93367000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37938598-C-T

93367448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37939173-T-C

93367448-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37939173-T-G

93367464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37939186-A-G

93367465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37939187-C-T

93367467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37939189-A-G

http://identifiers.org/hco/10/GRCh38#93367560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37939264-C-A

93367734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37939441-C-T

93367769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37939472-A-G

93369405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37939645-T-C

93369481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37939727-A-G

93369517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37939800-G-T

93369622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37939852-G-A

93369660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 37939890-G-A

93369660-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 37939890-G-C

93369660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 37939890-G-T

93369675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 37939905-T-C

93369856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37940088-G-A

93369856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37940088-G-T

93369857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37940089-G-T

93372065-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37940265-T-G

93372124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37940323-A-G

93372188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37940384-A-G

93372299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37940485-G-A

93372667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37941171-T-C

93372791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37941287-G-T

93372800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37941296-C-T

93372830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37941323-C-T

93372866-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37941357-A-T

93372941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 37941402-T-C

93372966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 37941427-T-C

93373133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37941591-T-C

93373246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37941685-C-T

93373251-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37941690-T-A

93373251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37941690-T-C

93373378-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37941813-T-A

93374364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37942439-G-A

93374478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37942558-C-T

http://identifiers.org/hco/10/GRCh38#93374678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37942733-C-A

http://identifiers.org/hco/10/GRCh38#93374685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37942740-C-A

93374685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37942740-C-T

93374711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37942769-G-A

93374711-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37942769-G-C

93374711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37942769-G-T

93374728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37942784-T-C

93374910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 37942962-G-A

93374922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 37942974-G-A

93374922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 37942974-G-T

93375012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37943057-C-T

93375020-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37943065-C-G

93375038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37943080-T-C

93375097-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37943166-G-C

93375097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37943166-G-T

93375130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37943201-C-T

http://identifiers.org/hco/10/GRCh38#93375897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37943404-C-A

93376494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37943927-A-G

93376519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37943956-G-T

93376526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37943963-T-C

93376633-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37944070-T-A

93376808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37944237-A-G

93376893-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37944502-T-A

93376959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37944551-C-T

93377005-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37944580-G-C

93377105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37944671-C-T

http://identifiers.org/hco/10/GRCh38#93377176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#37944739-C-A

93377176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37944739-C-T

http://identifiers.org/hco/10/GRCh38#93377231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37944807-C-A

93377248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 37944824-C-T

93377295-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37944863-T-A

93377295-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37944863-T-G

93377458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37945026-T-C

http://identifiers.org/hco/10/GRCh38#93377503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37945247-C-A

93377694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37945427-A-G

93377707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37945440-G-A

93377769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37945495-T-C

93377958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37945661-G-A

http://identifiers.org/hco/10/GRCh38#93378273-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37946007-C-A

93378273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37946007-C-T

93378321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37946058-G-A

http://identifiers.org/hco/10/GRCh38#93379062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37947392-C-A

93379104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37947434-C-T

93379246-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37947589-G-C

93379419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37947740-A-G

93379424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37947745-A-G

http://identifiers.org/hco/10/GRCh38#93379721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37948025-C-A

93379721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37948025-C-T

93379727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37948031-T-C

93380094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37948392-G-T

93380159-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37948548-T-G

93380253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37948634-T-C

93380535-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37948916-A-T

93380649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37948949-A-G

93380833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37949048-T-C

93380883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37949097-T-C

93380883-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37949097-T-G

93380893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37949106-G-A

http://identifiers.org/hco/10/GRCh38#93381077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37949237-C-A

93381077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37949237-C-T

93381140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37949288-G-A

93381147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37949295-A-G

93381173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37949321-G-A

93381173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37949321-G-T

http://identifiers.org/hco/10/GRCh38#93381185-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37949333-A-C

93381361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: synonymous variant
orthologous variants: 37949510-G-A

93381361-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: synonymous variant
orthologous variants: 37949510-G-C

http://identifiers.org/hco/10/GRCh38#93381364-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37949513-A-C

http://identifiers.org/hco/10/GRCh38#93381367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37949516-C-A

93381367-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: synonymous variant
orthologous variants: 37949516-C-G

93381367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: synonymous variant
orthologous variants: 37949516-C-T

93381414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37949563-A-G

http://identifiers.org/hco/10/GRCh38#93381415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37949564-C-A

93381454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37949603-G-T

93381511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37949661-G-T

http://identifiers.org/hco/10/GRCh38#93381529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37949679-C-A

93381537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37949687-T-C

93381537-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37949687-T-G

93381620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37949767-T-C

93381764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37949868-C-T

93381765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37949869-G-A

93382060-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37949985-A-T

93383085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37951726-G-A

93383085-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37951726-G-C

93383185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37951810-C-T

93383261-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37951853-G-C

93383366-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37951984-T-A

93383868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, undefined
orthologous variants: 37952831-G-A

93383942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37952901-G-A

93386690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37954063-T-C

93386745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37954116-T-C

93387055-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, undefined
orthologous variants: 37954393-T-G

http://identifiers.org/hco/10/GRCh38#93387346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37954641-C-A

93387509-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37954798-C-G

93387667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37955332-G-T

http://identifiers.org/hco/10/GRCh38#93387720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37955392-C-A

93387720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37955392-C-T

93387890-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: synonymous variant
orthologous variants: 37955557-G-C

93388240-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37955838-T-G

93388318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37955919-C-T

93388587-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37956168-G-C

http://identifiers.org/hco/10/GRCh38#93388604-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37956195-A-C

93388616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37956207-T-C

93388924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37956610-T-C

93388996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37956742-G-A

http://identifiers.org/hco/10/GRCh38#93388997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37956743-C-A

93388997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37956743-C-T

93389042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: synonymous variant
orthologous variants: 37956788-C-T

93389054-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: synonymous variant
orthologous variants: 37956800-G-C

93389197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37956942-T-C

93389299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37957047-G-A

93389486-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37957221-T-A

93389486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37957221-T-C

93389486-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37957221-T-G

93389768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37957481-G-A

93389800-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37957513-G-C

93392440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37957889-C-T

http://identifiers.org/hco/10/GRCh38#93392466-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37957915-A-C

93392501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37957936-T-C

93392672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37958110-C-T

http://identifiers.org/hco/10/GRCh38#93392792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37958227-C-A

93392792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37958227-C-T

93392868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37958306-A-G

93392993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37958471-C-T

93393047-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37958524-T-A

http://identifiers.org/hco/10/GRCh38#93393091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37958567-C-A

93393091-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37958567-C-G

93393091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37958567-C-T

93393095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37958571-T-C

93393225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37958690-G-A

93393422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37958902-T-C

93393642-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37959100-A-T

93393802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37959238-T-C

93393862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37959304-A-G

93394025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37959451-A-G

93394031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37959457-A-G

93394793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37959585-C-T

93394794-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37959586-T-A

93394838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37959630-A-G

93395837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37960066-T-C

93395938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37960112-T-C

93395938-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37960112-T-G

93395959-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37960123-C-G

93395966-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37960130-G-C

93396010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37960174-T-C

93396018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37960182-G-A

93396131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37960612-G-A

93396131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37960612-G-T

93396155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: synonymous variant
orthologous variants: 37960636-A-G

93396188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: synonymous variant
orthologous variants: 37960669-T-C

93396507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37960952-T-C

93396609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37961051-C-T

93396623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37961065-G-A

93396755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37962354-T-C

93396802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37962401-G-A

93396937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37962694-G-A

93396937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37962694-G-T

93396976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37962731-T-C

93396981-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37962736-A-T

93397009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37962764-C-T

93397034-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37962792-T-A

93397034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37962792-T-C

93397122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37962907-G-A

93397122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37962907-G-T

93397224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37963015-A-G

93397330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37963115-G-A

93397459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 37963377-G-A

93397729-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37963910-T-G

93397770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37963950-T-C

93397959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37964095-T-C

93398244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37964366-G-T

93398262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37964379-C-T

93398268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37964385-T-C

93398268-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37964385-T-G

93398545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37965120-G-A

93398668-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37965244-T-A

93399113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37965818-G-A

93399123-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37965828-G-C

93399367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37966073-A-G

http://identifiers.org/hco/10/GRCh38#93399449-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37966155-A-C

93399507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37966213-T-C

http://identifiers.org/hco/10/GRCh38#93399537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37966244-C-A

93399537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37966244-C-T

93400087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37966525-C-T

93400255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37966645-T-C

93400471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37966788-G-A

93400490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37966807-G-A

93400547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37966841-G-A

93401208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37968600-C-T

93401216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37968605-A-G

93401562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37968941-T-C

http://identifiers.org/hco/10/GRCh38#93401602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37968983-C-A

93401602-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37968983-C-G

93401687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37969051-T-C

93401687-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37969051-T-G

93401700-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37969056-T-G

93401815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37969133-G-A

93401830-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37969148-T-A

93402122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37969553-G-A

93402122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37969553-G-T

http://identifiers.org/hco/10/GRCh38#93402129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37969562-C-A

93402129-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37969562-C-G

93402129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37969562-C-T

93402375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37969811-T-C

93402377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37969813-G-T

http://identifiers.org/hco/10/GRCh38#93402468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37969857-C-A

93402468-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37969857-C-G

93402468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37969857-C-T

93402488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37969877-T-C

93402488-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37969877-T-G

http://identifiers.org/hco/10/GRCh38#93402494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37969883-C-A

93402494-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37969883-C-G

http://identifiers.org/hco/10/GRCh38#93402531-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37969924-A-C

http://identifiers.org/hco/10/GRCh38#93402619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37970012-C-A

93402647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37970041-G-A

http://identifiers.org/hco/10/GRCh38#93402714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37970129-C-A

93402714-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37970129-C-G

93402714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37970129-C-T

93402737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37970152-T-C

93402749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37970169-T-C

93402782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37970254-T-C

93402816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37970288-G-T

93403000-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37970458-T-G

93403157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37970608-G-A

93403241-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37970693-C-G

93403421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37970827-G-T

93403450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37970844-T-C

93403515-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37970909-A-T

93403541-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37970935-G-C

93403606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37970987-G-A

93403760-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37971133-T-A

93403946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37971319-G-A

93403946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37971319-G-T

93404181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: synonymous variant
orthologous variants: 37971561-C-T

93404255-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37971634-C-G

93404255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37971634-C-T

93404259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37971638-G-A

93404259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37971638-G-T

93404336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37971706-G-A

93404336-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37971706-G-T

93404344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37971714-A-G

93404434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37971758-G-T

http://identifiers.org/hco/10/GRCh38#93406884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37973781-C-A

93406886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37973783-G-A

93406886-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37973783-G-C

93406916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37973801-A-G

93407000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37973865-T-C

93407974-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37974163-T-G

http://identifiers.org/hco/10/GRCh38#93407984-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37974170-A-C

93407984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37974170-A-G

http://identifiers.org/hco/10/GRCh38#93408765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37974387-C-A

93408765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37974387-C-T

93408829-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: missense variant
orthologous variants: 37974451-G-C

93408980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37974601-G-A

93408980-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37974601-G-C

93409157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37974714-C-T

93409173-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37974729-C-G

93409173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37974729-C-T

93409223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37974776-C-T

http://identifiers.org/hco/10/GRCh38#93409455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37974980-C-A

93409455-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37974980-C-G

93409461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37974986-A-G

93409469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37974994-A-G

93409476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37975001-G-T

93409487-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37975012-T-A

93409487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37975012-T-C

93409490-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37975015-G-C

93409490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37975015-G-T

93409551-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37975082-C-G

93409576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: synonymous variant
orthologous variants: 37975100-G-A

93409576-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: missense variant
orthologous variants: 37975100-G-C

93409606-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 37975130-C-G

93409606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 37975130-C-T

93409748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37975271-T-C

93409810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37975336-A-G

http://identifiers.org/hco/10/GRCh38#93409869-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37975373-A-C

93409922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37975424-G-A

93410042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37975533-T-C

93410054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37975545-A-G

http://identifiers.org/hco/10/GRCh38#93410159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37975666-C-A

93410200-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37975706-T-G

93410273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37975771-G-A

93410461-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37975916-T-G

93410504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37975953-C-T

93410615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37976089-C-T

93413402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37976593-T-C

93413456-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37976646-C-G

93413675-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37976848-G-C

93413689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37976862-A-G

http://identifiers.org/hco/10/GRCh38#93417196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37978283-C-A

93417282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37978367-G-A

93417452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37978532-C-T

93417681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37978713-C-T

93418232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37979139-T-C

93420134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37980279-A-G

93420210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37980365-A-G

93420326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37980481-G-T

93420416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37980572-G-A

93420515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37980670-G-A

93420515-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37980670-G-C

93420515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37980670-G-T

93420691-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37980841-A-T

93420888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37981050-C-T

93422308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37982912-C-T

93422326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37982930-C-T

93422331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37982935-G-A

93425604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37983504-G-T

http://identifiers.org/hco/10/GRCh38#93425615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37983515-C-A

93425615-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37983515-C-G

93425615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37983515-C-T

93425659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37983557-G-T

93425665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37983564-A-G

http://identifiers.org/hco/10/GRCh38#93425683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37983582-C-A

93425683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron variant
orthologous variants: 37983582-C-T

93425757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37983636-T-C

93425839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37983713-G-A

93425839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37983713-G-T

93425846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37983720-T-C

93425888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37983761-G-A

93425888-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37983761-G-T

93425990-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37983774-A-T

93426033-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 37983816-C-G

93426044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, missense_variant
orthologous variants: 37983827-G-A

93426044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, missense_variant
orthologous variants: 37983827-G-T

http://identifiers.org/hco/10/GRCh38#93426055-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37983854-A-C

93426100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 37983899-A-G

93426100-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 37983899-A-T

93426111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 37983910-A-G

93426111-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 37983910-A-T

93426138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 37983937-G-A

93426138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 37983937-G-T

93426173-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37983972-T-A

93426185-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37983984-A-T

93426190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37983989-C-T

93426197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37983995-G-A

93426197-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37983995-G-C

93426197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37983995-G-T

93426209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37984007-G-A

93426209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37984007-G-T

http://identifiers.org/hco/10/GRCh38#93426217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37984015-C-A

93426410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37984186-C-T

93426412-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37984188-T-A

http://identifiers.org/hco/10/GRCh38#93427634-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37984454-A-C

93427641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37984461-T-C

93427723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37984547-G-A

93427767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37984624-C-T

93427987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37984775-T-C

93428293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37985004-C-T

93428300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37985011-C-T

93429490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37985790-G-A

93429669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37985969-C-T

93429827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37986100-T-C

93430214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37986275-G-A

93430271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37986332-T-C

93430853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37986584-C-T

93431478-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 37986734-G-C

93431540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37986796-A-G

93431541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37986797-T-C

http://identifiers.org/hco/10/GRCh38#93431561-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37986816-A-C

93431561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37986816-A-G

93431573-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37986829-A-T

93431578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37986834-G-T

93431618-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37986890-A-T

http://identifiers.org/hco/10/GRCh38#93432438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37987547-C-A

93432438-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37987547-C-G

93432438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37987547-C-T

93432507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37987616-T-C

93432602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37987705-T-C

93432646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37987749-C-T

93433500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37988272-C-T

93433547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37988329-G-A

93433584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37988364-T-C

93433775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37989404-G-A

http://identifiers.org/hco/10/GRCh38#93434010-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37989659-A-C

93434027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37989676-G-A

93434782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37989919-G-A

93434784-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37989921-A-T

93434833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37989976-T-C

93434967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37990090-G-A

93435136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37991324-C-T

http://identifiers.org/hco/10/GRCh38#93435299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37991501-C-A

93435299-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37991501-C-G

93436093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37992022-G-A

93436098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37992026-G-A

93436237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37992169-G-A

93436277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37992200-G-A

93436438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37992347-G-A

93436522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37992473-C-T

http://identifiers.org/hco/10/GRCh38#93436545-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37992494-A-C

93436745-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37992698-C-G

http://identifiers.org/hco/10/GRCh38#93436746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37992699-C-A

93436746-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37992699-C-G

93436848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37992796-G-A

93436946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37992896-A-G

93436946-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37992896-A-T

93437047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37992999-G-T

93437085-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37993032-T-G

93437220-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37993169-A-T

93437304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37993228-T-C

93437387-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37993308-G-C

93437407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37993330-C-T

93437411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37993334-T-C

93437437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37993366-G-T

93437564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37993472-T-C

93437639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37993545-G-A

93437639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37993545-G-T

93437823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37993718-G-A

93437927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37993820-G-A

93437939-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37993832-C-G

93437961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37993849-A-G

93437987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37993880-T-C

93438016-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37993909-A-T

93438104-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37993980-C-G

93438104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37993980-C-T

93438162-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37994056-G-C

93438284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37994176-G-A

http://identifiers.org/hco/10/GRCh38#93438313-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37994206-C-A

93438424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37994314-C-T

93438445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37994336-G-T

93438517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37994407-G-A

93438727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37994806-G-A

93438773-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37994840-A-T

93438820-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37994888-T-A

93439047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37995119-C-T

93439049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37995121-C-T

93439379-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37995432-T-G

http://identifiers.org/hco/10/GRCh38#93439564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37995619-C-A

93439564-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37995619-C-G

93439564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37995619-C-T

93439623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37995671-G-A

93439623-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37995671-G-C

93439672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37995717-T-C

93439708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37995753-G-A

93439794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37995835-C-T

93439827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37995855-A-G

93440643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37997359-G-A

93440677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37997393-C-T

93442043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37999647-G-A

93442043-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37999647-G-C

93442043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37999647-G-T

http://identifiers.org/hco/10/GRCh38#93442051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#37999655-C-A

93442071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37999675-T-C

93442122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37999717-G-A

93442149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37999743-G-A

93442163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37999756-C-T

93442175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37999768-A-G

93442486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38000059-C-T

93442583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38000156-C-T

93442621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38000194-C-T

93442648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38000271-G-A

93442705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38000331-T-C

93442706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38000332-A-G

93442797-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38000424-A-T

93442824-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38000444-T-A

93442825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38000445-G-A

93443538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38000568-G-A

93443538-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38000568-G-C

93443569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38000603-C-T

93443571-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38000605-C-G

93443672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38000687-G-A

93443679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38000694-C-T

http://identifiers.org/hco/10/GRCh38#93443713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38000725-C-A

93443950-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38000970-C-G

93444040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38001056-G-A

93444056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38001070-G-A

93444061-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38001075-C-G

93444134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38001139-G-A

93444162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38001168-T-C

93444227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38001233-C-T

93444334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38002895-G-A

93444521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38003067-C-T

93444563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38003087-A-G

93444712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38003229-C-T

93445033-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38003522-A-T

93445042-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38003528-T-G

93445203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38003704-A-G

93445215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38003716-T-C

93445227-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38003728-T-A

93445322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38003797-G-A

93445387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38003842-C-T

93445452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38003900-C-T

http://identifiers.org/hco/10/GRCh38#93445594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38004023-C-A

93445594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38004023-C-T

93446026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38004415-T-C

93446046-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38004435-T-A

93446190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38004559-G-A

93446196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38004565-G-A

93446201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38004570-G-A

93446201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38004570-G-T

93446318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38004671-A-G

93446318-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38004671-A-T

93446463-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38005218-C-G

93446528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38005283-G-T

93446550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38005304-G-A

http://identifiers.org/hco/10/GRCh38#93449338-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38008670-A-C

93450654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38009929-G-A

http://identifiers.org/hco/10/GRCh38#93450660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38009937-C-A

93450660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38009937-C-T

93450691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38009954-T-C

93450709-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38009971-C-G

http://identifiers.org/hco/10/GRCh38#93450747-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38009998-A-C

93450899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38010148-T-C

93451823-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38010769-T-G

93451900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38010836-T-C

93451908-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38010844-T-G

http://identifiers.org/hco/10/GRCh38#93451959-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38010904-A-C

93452002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38010953-G-T

93452010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38010961-G-A

http://identifiers.org/hco/10/GRCh38#93452032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38010983-C-A

93452089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38011040-C-T

http://identifiers.org/hco/10/GRCh38#93452097-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38011048-A-C

93452168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38011113-G-A

93452168-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38011113-G-C

93452168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38011113-G-T

93452278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38011185-G-A

93452278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38011185-G-T

93452284-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38011191-A-T

93454418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38011864-C-T

93454453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38011885-A-G

93455727-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38012157-G-C

93455735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38012167-A-G

93456016-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38012396-T-A

93456016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38012396-T-C

93456016-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38012396-T-G

93456994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38012904-G-A

93456994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38012904-G-T

93457009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38012923-T-C

http://identifiers.org/hco/10/GRCh38#93457031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38012945-C-A

93457031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38012945-C-T

93457077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38012991-A-G

http://identifiers.org/hco/10/GRCh38#93457083-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38012997-A-C

93457160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38013085-A-G

93457160-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38013085-A-T

93457167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38013092-G-A

http://identifiers.org/hco/10/GRCh38#93457232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38013156-C-A

93457324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38013240-C-T

93457597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38013500-A-G

93457610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38013513-T-C

93457676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38013553-C-T

93458817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38013764-T-C

93461233-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38014103-C-G

93461233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38014103-C-T

93461523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38014408-C-T

93461768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38014603-G-A

93461891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38014728-A-G

93462532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38014999-C-T

93462634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38015101-G-A

93462804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38015280-A-G

93462810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38015287-T-C

93462936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38015402-A-G

http://identifiers.org/hco/10/GRCh38#93463201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38015622-C-A

93465174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38015934-G-A

93465333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38016066-C-T

93465831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38016414-C-T

93465867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38016450-G-A

93465881-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38016464-G-C

93465961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38016528-C-T

93466008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38016573-T-C

93466054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38016616-G-A

93466084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38016638-G-A

http://identifiers.org/hco/10/GRCh38#93466121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38016696-C-A

93466278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38016834-T-C

93466364-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38016914-C-G

93466364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38016914-C-T

93466382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38016931-G-A

93466445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38016991-G-A

93468210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38017939-C-T

93468297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38018016-G-A

93468297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38018016-G-T

93468326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38018037-G-A

93468398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38018110-C-T

93468642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38018313-G-T

93468739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38018406-G-A

93468746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38018413-A-G

93468799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38018464-T-C

93468810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38018475-G-T

93468875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38018539-G-A

93468994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38018661-G-A

93469010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38018677-C-T

93470739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38021074-G-A

93470766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38021101-G-A

93471029-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38021325-A-T

93471030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38021326-T-C

93471037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38021333-C-T

93471044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38021340-G-T

93471060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38021357-T-C

93471085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38021382-G-A

93471105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38021416-G-A

93471182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38021499-G-A

93471215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38021532-T-C

93471305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38021624-G-T

93471465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38021788-G-A

93471500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38021823-G-A

93471500-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38021823-G-C

93471528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38021851-C-T

93472788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38023396-C-T

93472845-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38023450-C-G

93472845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38023450-C-T

93472963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38023519-T-C

93472987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38023542-C-T

93473157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38023712-G-A

93473260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38023810-C-T

93473329-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38023881-T-G

93473684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38024108-A-G

93473769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38024190-T-C

93474107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38024485-A-G

93474263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38024616-C-T

93475086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38026074-G-A

93475142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38026135-G-T

93475213-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38026210-T-A

93475284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38026270-A-G

http://identifiers.org/hco/10/GRCh38#93475298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38026284-C-A

93475329-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38026336-C-G

93475329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38026336-C-T

93475391-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38026399-G-C

93475698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38026716-C-T

93475935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38026921-C-T

93476138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38027116-T-C

93477070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38027897-A-G

93477129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38027961-C-T

93477182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38028019-G-T

http://identifiers.org/hco/10/GRCh38#93478069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38028370-C-A

http://identifiers.org/hco/10/GRCh38#93478086-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38028387-C-A

93478086-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38028387-C-G

93478086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38028387-C-T

93478116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38028419-T-C

93478195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38028616-G-A

93478195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38028616-G-T

http://identifiers.org/hco/10/GRCh38#93478205-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38028642-A-C

93478205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38028642-A-G

http://identifiers.org/hco/10/GRCh38#93478219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38028707-C-A

93478219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38028707-C-T

http://identifiers.org/hco/10/GRCh38#93478246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38028732-C-A

93478247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38028733-T-C

93478247-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38028733-T-G

http://identifiers.org/hco/10/GRCh38#93478260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38028745-C-A

93478260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38028745-C-T

http://identifiers.org/hco/10/GRCh38#93478283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38028768-C-A

93478283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38028768-C-T

93478304-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38028789-T-A

93478304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38028789-T-C

93478304-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38028789-T-G

http://identifiers.org/hco/10/GRCh38#93478317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38028801-C-A

93478317-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38028801-C-G

93478317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38028801-C-T

http://identifiers.org/hco/10/GRCh38#93478366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38028846-C-A

93478393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38028860-T-C

http://identifiers.org/hco/10/GRCh38#93478441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38028907-C-A

93478441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38028907-C-T

http://identifiers.org/hco/10/GRCh38#93478446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38028910-C-A

93478446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38028910-C-T

http://identifiers.org/hco/10/GRCh38#93478451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38028915-C-A

93478451-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38028915-C-G

93478451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38028915-C-T

93478485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38028934-A-G

http://identifiers.org/hco/10/GRCh38#93478969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38029450-C-A

93478969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38029450-C-T

93479471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38029640-C-T

93479719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38030003-G-A

93480066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38030335-G-A

93480214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38030466-T-C

http://identifiers.org/hco/10/GRCh38#93480902-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38030745-A-C

93480932-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38030775-C-G

93480932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38030775-C-T

93481040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38030861-T-C

http://identifiers.org/hco/10/GRCh38#93481447-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38031087-A-C

93481650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38031247-C-T

http://identifiers.org/hco/10/GRCh38#93481921-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38031497-A-C

93481922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38031498-A-G

93481955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38031532-A-G

93482055-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38031629-A-T

93482138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3656
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38031715-C-T