http://identifiers.org/hco/5/GRCh38#38258476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7427830-C-A

38258476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7427830-C-T

http://identifiers.org/hco/5/GRCh38#38258478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7427828-C-A

38258478-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7427828-C-G

38258478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7427828-C-T

38258545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7427762-T-C

38258598-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 7427709-T-A

38258598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 7427709-T-C

38258598-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 7427709-T-G

38258605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 7427702-A-G

http://identifiers.org/hco/5/GRCh38#38258652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7427654-C-A

38258652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 7427654-C-T

38258677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 7427641-G-A

38258677-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 7427641-G-C

38258710-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 7427608-T-A

38258710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 7427608-T-C

38258832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 7427486-A-G

38258876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7427441-C-T

http://identifiers.org/hco/5/GRCh38#38258942-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7427381-C-A

38258969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7427355-T-C

http://identifiers.org/hco/5/GRCh38#38258970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7427354-C-A

38258970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7427354-C-T

38258982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7427342-G-A

38258982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7427342-G-T

38259113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7427218-G-A

38259113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7427218-G-T

38259283-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7427030-C-G

38259517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7426795-C-T

38259976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7426324-G-A

38260010-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7426290-G-C

38260023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7426276-G-T

38260228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7426082-T-C

38260434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7425904-A-G

38260576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7425752-A-G

38261067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7425266-C-T

38261351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7425024-A-G

38261641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7424747-G-A

38261641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7424747-G-T

38261783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7424627-C-T

38261834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7424579-A-G

38261864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7424549-T-C

38262077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7424427-A-G

38262392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7424149-T-C

38262425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7424116-T-C

38262495-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7423965-G-C

38262575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7423885-T-C

http://identifiers.org/hco/5/GRCh38#38262686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7423767-C-A

38262686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7423767-C-T

38262722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7423729-A-G

38262841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7423619-A-G

38262873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7423590-G-A

38264548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7421800-G-T

38264586-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7421774-T-G

38264698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7421669-T-C

38264935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7421389-G-A

38265285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7421049-G-A

38265322-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7421014-C-G

38265353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7420977-T-C

38265376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7420951-C-T

http://identifiers.org/hco/5/GRCh38#38265427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7420891-C-A

38265427-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7420891-C-G

38265445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7420873-G-A

38265541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 7420683-G-A

38265683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 7420526-A-G

38265780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 7420434-G-T

38266201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7419817-T-C

38266267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7419766-G-A

38266318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7419703-A-G

38266321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7419700-C-T

38266325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7419696-A-G

38266586-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7419462-A-T

38266926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7419081-T-C

http://identifiers.org/hco/5/GRCh38#38267091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7418258-C-A

38267609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7417716-A-G

38267848-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7417311-T-G

38267957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7417216-G-A

38268208-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7416824-T-A

38268280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7416754-C-T

38268290-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7416745-T-G

38268355-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7416688-A-T

38268370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7416673-G-T

38268431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7416611-A-G

38268476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7416566-A-G

38268497-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7416545-C-G

38268578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7416464-C-T

38268665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7416392-T-C

38269824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7414711-G-A

38270836-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7413754-G-C

38270885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7413705-G-T

38270941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7413647-T-C

38271041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7413548-G-A

38271162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7413425-G-T

38271313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7413293-C-T

38271414-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7412800-T-A

38271720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7412496-C-T

38271922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7412281-A-G

38272359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7411841-C-T

38272387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7411813-A-G

38272574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7411635-A-G

http://identifiers.org/hco/5/GRCh38#38272665-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7411544-A-C

38272665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7411544-A-G

38280220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7411032-G-A

38280266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7410976-C-T

38280286-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7410927-T-G

38280386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7410755-C-T

38280635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7410577-G-A

38280996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7410223-G-A

38281043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7410177-G-A

38281059-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7410161-T-G

38281129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7410092-C-T

http://identifiers.org/hco/5/GRCh38#38281556-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7409677-A-C

38281556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7409677-A-G

38281595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7409638-T-C

38281682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7409401-A-G

38281710-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7409373-G-C

38281748-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7409344-C-G

38281748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7409344-C-T

38281832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7409268-T-C

38281921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7409187-G-A

38282086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7409039-T-C

http://identifiers.org/hco/5/GRCh38#38282114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7408984-C-A

38282127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7408970-G-T

38282216-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7408896-T-A

38282392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7408721-G-T

38282408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7408706-A-G

38282441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7408687-T-C

38282449-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7408677-G-T

http://identifiers.org/hco/5/GRCh38#38282453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7408673-C-A

38282453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7408673-C-T

38282507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7408629-A-G

38282525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7408611-A-G

38282575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7408553-C-T

http://identifiers.org/hco/5/GRCh38#38282590-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7408539-A-C

38282590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7408539-A-G

38282635-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7408474-G-C

38282672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7408436-A-G

38282730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7408388-C-T

38282739-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7408379-T-G

38282811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7408338-C-T

38283244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7407753-T-C

38283460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7407557-G-A

http://identifiers.org/hco/5/GRCh38#38283539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7407478-C-A

38283553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7407464-T-C

38283644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7407401-G-A

38283644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7407401-G-T

http://identifiers.org/hco/5/GRCh38#38283723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7407319-C-A

38283860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7407198-G-T

http://identifiers.org/hco/5/GRCh38#38283903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7407160-C-A

38283925-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 7407140-T-A

38284009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7407054-G-A

38284010-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7407053-G-C

38284010-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7407053-G-T

38284178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7406935-T-C

38284515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7406584-C-T

http://identifiers.org/hco/5/GRCh38#38284628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7406464-C-A

38284675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7406419-C-T

38284980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7405635-A-G

http://identifiers.org/hco/5/GRCh38#38285067-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7405550-A-C

38285570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7404987-G-T

38285628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7404924-T-C

38285689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 7404839-A-G

38285776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7404767-A-G

38285881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7404645-T-C

38286038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7404300-G-A

38286059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7404277-A-G

38286132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7404201-T-C

38286160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7404173-A-G

38286196-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7404136-A-T

38286340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7404002-G-A

38286421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7403926-C-T

http://identifiers.org/hco/5/GRCh38#38286449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7403899-C-A

38286499-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7403849-T-A

38286709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7403650-G-A

http://identifiers.org/hco/5/GRCh38#38286712-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7403647-A-C

38286718-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7403641-C-G

38286759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7403609-C-T

38286839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7403533-G-A

38286938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7403453-C-T

38287022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7403370-C-T

38287206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7403187-C-T

38287771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7402871-G-T

38287973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7402676-C-T

http://identifiers.org/hco/5/GRCh38#38291123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7401484-C-A

38291277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7401345-T-C

http://identifiers.org/hco/5/GRCh38#38291373-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7401259-A-C

38291526-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 7401108-G-C

38291527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 7401107-C-T

38291947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7400681-C-T

38291968-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7400660-T-A

38292005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7400624-G-A

38292351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7399997-G-T

38292366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7399982-G-T

38292510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7399838-G-A

38292602-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7399743-T-G

http://identifiers.org/hco/5/GRCh38#38292929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7398937-C-A

38293005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7398871-G-A

38293057-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7398818-T-G

38293219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7398645-A-G

38293249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7398615-A-G

38293256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7398608-G-T

38293626-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7398274-A-T

38294265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7397720-C-T

38294494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7397444-C-T

38294505-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7397433-G-C

38294605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7397368-A-G

38294620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7397353-C-T

38295442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7389639-A-G

38295442-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7389639-A-T

38295445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7389636-A-G

http://identifiers.org/hco/5/GRCh38#38295484-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7389597-A-C

38295581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7389508-A-G

38295685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7389408-A-G

38295962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7389147-A-G

38296159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7388992-G-A

38296222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7388925-G-A

38296235-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7388906-C-G

38296235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7388906-C-T

38298143-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7382334-A-T

38298225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7382252-C-T

38298361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7382124-C-T

38298403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7382082-T-C

38301194-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7378641-A-T

38301724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7378147-G-A

38301733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7378138-G-A

38301836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7378034-G-A

http://identifiers.org/hco/5/GRCh38#38301880-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7377991-A-C

38302635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7377607-C-T

38302681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7377562-G-A

38302757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7377498-G-T

38302777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7377478-G-A

38302913-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7377345-A-T

38303130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7377147-C-T

38303316-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7375868-A-T

38304197-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7375052-A-T

38304383-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7374859-A-T

38304446-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7374796-G-T

38304511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7374733-A-G

http://identifiers.org/hco/5/GRCh38#38304579-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7374664-A-C

38306279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7373946-C-T

38306714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7373542-A-G

38307756-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7373055-A-T

38307786-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7373022-T-G

38308408-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7372878-G-C

http://identifiers.org/hco/5/GRCh38#38308532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7372785-C-A

38311306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7371265-C-T

http://identifiers.org/hco/5/GRCh38#38311594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7370983-C-A

38311736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7370852-T-C

38312006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7370589-T-C

38313740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7368529-A-G

38313902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7368384-G-A

38313902-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7368384-G-C

38314055-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7368239-T-G

38314407-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7367894-G-C

38314616-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7367683-G-C

38314616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7367683-G-T

38314919-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7367421-C-G

38315445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7366904-C-T

38315544-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7366772-G-C

38317288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7365887-A-G

38317522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7365710-A-G

38317524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7365708-G-T

38322856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7361798-C-T

38323023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7361632-T-C

38323662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7360979-T-C

38323697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7360941-A-G

38324019-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7360858-G-C

38324165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7360790-T-C

38324165-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7360790-T-G

38324271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7360688-C-T

38324429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7360549-C-T

38324635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7360364-T-C

38324668-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7360332-A-T

38324711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7360303-A-G

38324749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7360284-G-T

38325028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7360054-G-A

38325029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7360053-C-T

38325102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7359984-A-G

38325178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7359910-C-T

38325731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7359113-A-G

38325776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7359052-C-T

http://identifiers.org/hco/5/GRCh38#38327022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7358192-C-A

38327157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7358077-T-C

38327293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7357951-A-G

38327450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7357781-G-A

38327489-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7357740-C-G

38327614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7357590-T-C

http://identifiers.org/hco/5/GRCh38#38327929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7357298-C-A

38327976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7357250-T-C

38328800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7356853-C-T

http://identifiers.org/hco/5/GRCh38#38328801-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7356852-A-C

38328801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7356852-A-G

38328925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7356728-G-A

38328958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7356697-T-C

38328958-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7356697-T-G

38329296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7356662-A-G

38329300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7356658-A-G

38329567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7356384-T-C

38329652-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7356233-G-C

38329665-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7356223-T-G

38329895-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7355984-G-T

38329934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7355938-G-A

38330505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7355223-T-C

http://identifiers.org/hco/5/GRCh38#38330535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7355167-C-A

38330535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7355167-C-T

38330590-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7355114-G-C

38330871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7354841-C-T

38334602-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7350950-C-G

38334781-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7350793-T-A

38334970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7350614-C-T

38335028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7350554-G-A

38335035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7350547-C-T

38335049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7350517-G-A

38335211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7350411-A-G

38335347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7350279-G-A

http://identifiers.org/hco/5/GRCh38#38335348-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7350278-A-C

38335397-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7350228-C-G

38335424-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7350203-T-A

38335552-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7350075-T-A

38335886-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7349558-A-T

38335908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7349536-T-C

38336236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7349114-T-C

38336236-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7349114-T-G

38336901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7348983-C-T

38337145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7348194-A-G

38337145-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7348194-A-T

38337237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7348109-A-G

38337293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7348047-G-A

38337303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7348034-T-C

38337376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7347959-G-A

38337376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7347959-G-T

38337481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7347866-T-C

38337553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 7347796-G-A

38337553-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 7347796-G-C

38337599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 7347750-G-A

38338457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7346179-T-C

38338649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7346010-T-C

38338739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 7345920-G-A

38338750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 7345909-G-A

38338850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7345809-G-T

38338884-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7345775-T-G

38338892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7345769-G-A

38338892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7345769-G-T

38338905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7345764-A-G

38338944-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7345725-C-G

38339832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7344893-C-T

38339865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7344854-G-A

38339978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7344628-G-T

38339988-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7344617-G-T

38340371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7344255-A-G

38340397-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7344230-T-A

38340397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7344230-T-C

38340408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7344217-C-T

38340794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7343585-T-C

38341022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7343419-G-A

http://identifiers.org/hco/5/GRCh38#38341031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7343374-C-A

38341355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7343134-A-G

http://identifiers.org/hco/5/GRCh38#38341478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7343045-C-A

38341771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7342750-A-G

38341956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7342599-C-T

38342101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7342465-C-T

38342512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7342106-A-G

38342588-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7342011-T-A

38342588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7342011-T-C

http://identifiers.org/hco/5/GRCh38#38342671-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7341928-A-C

38343022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7341556-C-T

38344797-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7341051-A-T

38345004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7340844-G-A

38345027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7340824-A-G

38345125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7340716-C-T

38345317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7340539-A-G

38345397-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7340461-G-T

38345403-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7340437-C-G

38345403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7340437-C-T

38345702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7340121-A-G

38345703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7340120-G-T

38345821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7340007-G-T

38345889-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7339935-T-A

http://identifiers.org/hco/5/GRCh38#38345972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7339851-C-A

http://identifiers.org/hco/5/GRCh38#38346032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7339789-C-A

38346032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7339789-C-T

38346177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7339672-A-G

38346209-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7339637-T-G

38346231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7339613-A-G

38346321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7339508-A-G

38346330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7339500-A-G

38346353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7339477-C-T

38346996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7338619-C-T

38347009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7338606-C-T

38349331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7335938-G-A

38349439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7335834-C-T

38349443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7335830-G-T

http://identifiers.org/hco/5/GRCh38#38349726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7335570-C-A

38349726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7335570-C-T

38349936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7335397-G-A

38349936-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7335397-G-C

38349954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7335388-C-T

38349988-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7335377-G-C

38350036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7335330-T-C

38350139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7335231-C-T

38350170-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7335205-C-G

38350264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7335141-T-C

38350376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7335030-A-G

http://identifiers.org/hco/5/GRCh38#38350405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7335001-C-A

38350405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7335001-C-T

38350638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7334560-A-G

38350639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7334559-T-C

38350642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7334556-A-G

38350763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7334448-C-T

38351525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7334129-A-G

38351605-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7334067-G-C

38351920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7333767-G-A

38352095-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7333610-T-A

38352095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7333610-T-C

38352095-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7333610-T-G

38352101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7333604-G-A

38352101-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7333604-G-T

38352143-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7333592-T-G

38352246-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 7333489-T-G

38352910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7333171-T-C

38353083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7333002-A-G

38353391-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7332738-G-C

38353620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7332550-A-G

38353882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7332309-G-A

38353956-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7332236-G-C

38353962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7332230-G-A

38354400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7331700-G-A

38361779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7331122-G-A

38361787-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7331114-C-G

38362351-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7330382-T-A

38362401-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7330324-G-C

38362910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7329750-T-C

38362973-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7329681-T-G

38363199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7329469-A-G

38363860-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7328815-T-G

38364149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7328587-G-A

38364151-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7328585-A-T

38364193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7328544-G-A

38364527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7328186-G-A

38364591-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7328122-G-C

http://identifiers.org/hco/5/GRCh38#38364697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7328016-C-A

38364924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7327800-G-A

http://identifiers.org/hco/5/GRCh38#38365100-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7327622-A-C

http://identifiers.org/hco/5/GRCh38#38365249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7327436-C-A

38365249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7327436-C-T

38365281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7327383-C-T

http://identifiers.org/hco/5/GRCh38#38366387-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7323188-A-C

38366531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7323096-G-T

38366560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7323068-T-C

38367122-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7322574-C-G

38367124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7322572-C-T

38367693-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7322445-A-T

38367714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7322423-G-T

38368021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7322115-G-T

38368072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7322064-A-G

http://identifiers.org/hco/5/GRCh38#38368160-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7321983-A-C

38368162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7321981-G-T

38368250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7321893-G-A

38368250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7321893-G-T

http://identifiers.org/hco/5/GRCh38#38368255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7321888-C-A

38368700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7321460-A-G

38368717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7321443-G-A

38368920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7321232-A-G

http://identifiers.org/hco/5/GRCh38#38369048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7321046-C-A

38369098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7321000-C-T

http://identifiers.org/hco/5/GRCh38#38369441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7320314-C-A

38369488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7320265-G-A

38369744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7319978-T-C

38370019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7319705-T-C

38370055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7319669-A-G

38370147-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7319576-T-A

http://identifiers.org/hco/5/GRCh38#38370200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7319523-C-A

http://identifiers.org/hco/5/GRCh38#38370258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7319465-C-A

http://identifiers.org/hco/5/GRCh38#38370263-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7319460-C-A

38370263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7319460-C-T

38370290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 7319435-A-G

38370332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: synonymous variant
orthologous variants: 7319393-G-A

http://identifiers.org/hco/5/GRCh38#38370491-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7319234-A-C

38370491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7319234-A-G

http://identifiers.org/hco/5/GRCh38#38370516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7319209-C-A

38370517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7319208-T-C

38370705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7319016-G-T

38370876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7318698-A-G

38370904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7318674-G-A

38370950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7318622-G-A

http://identifiers.org/hco/5/GRCh38#38371263-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7318301-A-C

38371520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7318057-A-G

38371520-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7318057-A-T

38371550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7318025-C-T

38371660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7317953-G-A

38371660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7317953-G-T

38371830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7317773-T-C

38371845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7317758-G-A

38372513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7317431-A-G

38372614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7317323-T-C

38372752-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7316447-T-A

38373218-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7316068-A-T

38373302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7315981-C-T

38375793-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7315530-G-C

38375793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7315530-G-T

http://identifiers.org/hco/5/GRCh38#38375804-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7315519-A-C

http://identifiers.org/hco/5/GRCh38#38375857-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7315468-A-C

38375877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7315444-A-G

38375955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7315365-C-T

38375990-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7315332-G-C

38376098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7315215-T-C

38376161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7315155-T-C

38376350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7314968-G-A

38376372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7314946-A-G

38376384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7314942-A-G

38376408-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7314924-C-G

http://identifiers.org/hco/5/GRCh38#38376463-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7314869-A-C

38377881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7314141-T-C

38377903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7314119-A-G

38377903-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7314119-A-T

38378009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7314014-A-G

38378266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7313829-T-C

38378455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7313344-C-T

38378468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7313332-G-A

38378487-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7313312-G-C

38378530-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7313275-G-C

38378582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7313231-G-A

38378742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7313094-C-T

38378894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7312970-G-A

38378909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7312951-C-T

38379070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7312787-A-G

38379298-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7312560-C-G

38379298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7312560-C-T

http://identifiers.org/hco/5/GRCh38#38380131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7311616-C-A

38382056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7301349-T-C

38382287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7301144-T-C

38382964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, undefined
orthologous variants: 7293572-G-A

38383085-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, undefined
orthologous variants: 7293434-T-A

38383183-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, undefined
orthologous variants: 7293332-T-A

38383183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, undefined
orthologous variants: 7293332-T-C

38383183-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, undefined
orthologous variants: 7293332-T-G

38383280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7293263-T-C

38383338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7293225-C-T

http://identifiers.org/hco/5/GRCh38#38384434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7292060-C-A

38384559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7291919-A-G

38384584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7291895-C-T

38387041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7291063-G-A

http://identifiers.org/hco/5/GRCh38#38387207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7290899-C-A

http://identifiers.org/hco/5/GRCh38#38387353-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7290786-C-A

http://identifiers.org/hco/5/GRCh38#38387774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7290398-C-A

38387774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7290398-C-T

38387801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7290371-G-A

38388963-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7288552-A-T

38389137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7288389-T-C

38389307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7288246-A-G

38389333-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7288221-C-G

38395721-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7286626-T-G

38395749-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7286594-C-G

http://identifiers.org/hco/5/GRCh38#38399696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7285676-C-A

38399701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7285671-A-G

38399702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7285670-G-A

38399745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7285624-A-G

38399811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7285550-T-C

38399821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7285536-G-T

38400184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7284868-A-G

38400253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7284804-T-C

38400507-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7284532-T-G

38400522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7284517-A-G

http://identifiers.org/hco/5/GRCh38#38400787-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7284275-A-C

38406066-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7284083-T-G

38406072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7284077-A-G

38406148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 7284001-C-T

38406150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, missense_variant
orthologous variants: 7283999-G-A

38406150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, missense_variant
orthologous variants: 7283999-G-T

38406225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, missense_variant
orthologous variants: 7283924-A-G

38406225-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, missense_variant
orthologous variants: 7283924-A-T

http://identifiers.org/hco/5/GRCh38#38406246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7283904-C-A

38406246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7283904-C-T

http://identifiers.org/hco/5/GRCh38#38406255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7283895-C-A

38406255-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7283895-C-G

38406313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7283840-G-A

38406313-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7283840-G-C

http://identifiers.org/hco/5/GRCh38#38406378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7283775-C-A

38406378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7283775-C-T

38406530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7283539-A-G

http://identifiers.org/hco/5/GRCh38#38406686-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7283365-A-C

38406699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7283353-T-C

38406855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, missense_variant
orthologous variants: 7283198-G-A

38406893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 7283160-T-C

http://identifiers.org/hco/5/GRCh38#38406910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7283143-C-A

38406910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, missense_variant
orthologous variants: 7283143-C-T

http://identifiers.org/hco/5/GRCh38#38406933-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7283120-A-C

38407172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7282884-G-A

38407172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7282884-G-T

38407208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7282857-A-G

38407229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7282836-T-C

http://identifiers.org/hco/5/GRCh38#38407242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7282823-C-A

38407394-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7282671-A-T

http://identifiers.org/hco/5/GRCh38#38407468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7282585-C-A

38407468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7282585-C-T

38407488-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7282565-A-T

38407600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7282194-C-T

38407675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7282114-A-G

38407772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7282017-G-A

38407772-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7282017-G-C

38407780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7282009-T-C

38407968-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7281849-T-A

38407968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7281849-T-C

38407968-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7281849-T-G

38408012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7281820-G-A

38408012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7281820-G-T

38408017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7281815-G-T

38408051-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7281781-T-A

38408051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7281781-T-C

38408093-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7281754-G-C

38408195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7281680-C-T

38408630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7281140-A-G

38408731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7281029-A-G

http://identifiers.org/hco/5/GRCh38#38408869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7280894-C-A

38408869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7280894-C-T

http://identifiers.org/hco/5/GRCh38#38408925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7280840-C-A

38408925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7280840-C-T

38408942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7280827-G-A

38408965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7280812-T-C

38408989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7280788-T-C

38409010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, missense_variant
orthologous variants: 7280767-G-A

38409010-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, missense_variant
orthologous variants: 7280767-G-T

http://identifiers.org/hco/5/GRCh38#38409049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7280728-C-A

38409049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, missense_variant
orthologous variants: 7280728-C-T

38409064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, missense_variant
orthologous variants: 7280713-T-C

http://identifiers.org/hco/5/GRCh38#38409116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7280661-C-A

38409208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7280590-G-T

38409217-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7280581-A-T

38409252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7280545-A-G

38409299-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7280498-T-G

38409680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7280374-T-C

38409693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7280359-G-A

38409811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7280226-G-A

38409817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7280220-C-T

http://identifiers.org/hco/5/GRCh38#38409825-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7280212-A-C

38409825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7280212-A-G

38410093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7279982-C-T

38410120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7279959-C-T

38410133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7279947-C-T

38412463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7279698-G-T

38412464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7279697-G-A

38412464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7279697-G-T

38412486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7279675-C-T

38412494-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7279663-T-G

38412661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7279497-C-T

http://identifiers.org/hco/5/GRCh38#38412688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7279470-C-A

38412688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7279470-C-T

38412760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7279433-T-C

38412760-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7279433-T-G

38412796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7279400-T-C

38412796-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7279400-T-G

38412797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7279399-G-A

38412797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7279399-G-T

38412840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7279364-G-A

38412866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7279341-G-A

38412870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7279337-A-G

38412952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7279280-A-G

38412952-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7279280-A-T

http://identifiers.org/hco/5/GRCh38#38413359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7279209-C-A

38413362-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7279206-G-C

38413387-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7279190-C-G

38413387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7279190-C-T

38413524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7279059-A-G

38416113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7278095-G-A

38416292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7277927-G-A

38416324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7277892-G-A

38416391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7277826-C-T

38416642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7277679-G-A

38416689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7277658-A-G

38416753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7277601-A-G

38416768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7277586-C-T

38417404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7277319-C-T

http://identifiers.org/hco/5/GRCh38#38417479-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7277249-A-C

38417681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7277050-G-A

38417752-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7276980-C-G

38417752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7276980-C-T

38417759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7276973-G-A

38417823-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7276925-C-G

38417848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7276900-C-T

38417878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7276872-A-G

38417883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7276867-G-A

http://identifiers.org/hco/5/GRCh38#38417922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7276821-C-A

38417922-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7276821-C-G

38417922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7276821-C-T

38418013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7276731-G-A

http://identifiers.org/hco/5/GRCh38#38418120-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7276614-A-C

38418120-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, missense_variant
orthologous variants: 7276614-A-T

38418274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7276460-G-A

38418274-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7276460-G-C

http://identifiers.org/hco/5/GRCh38#38418314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7276444-C-A

38418314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7276444-C-T

38418395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7276400-A-G

http://identifiers.org/hco/5/GRCh38#38418402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7276399-C-A

38418402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7276399-C-T

38419018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7275833-C-T

38424360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7273913-T-C

38424373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7273900-T-C

38424431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7273850-C-T

38424736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7273580-T-C

http://identifiers.org/hco/5/GRCh38#38424848-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7273484-A-C

38424848-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7273484-A-T

38424850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7273482-A-G

38424865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7273466-A-G

38425162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7273207-A-G

38425730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7273071-C-T

38425772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7273029-T-C

http://identifiers.org/hco/5/GRCh38#38426261-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7272836-A-C

38426261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7272836-A-G

38426552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7272540-G-A

38426637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7272467-T-C

38426685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7272425-A-G

38426685-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7272425-A-T

38426700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7272409-T-C

38426746-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7272385-A-T

http://identifiers.org/hco/5/GRCh38#38426859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7272271-C-A

38426871-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7272259-A-T

38426991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7272142-C-T

38427004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 7272129-T-C

38427042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 7272091-C-T

38427131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 7272002-T-C

38427182-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 7271951-C-G

38427376-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7271769-T-A

38427376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7271769-T-C

38427394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7271760-G-A

38427394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7271760-G-T

38427489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7271493-G-A

38427489-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7271493-G-C

38427489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7271493-G-T

38427505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7271476-G-A

38427505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7271476-G-T

38427928-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7270975-T-G

38427934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7270969-A-G

38427940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7270957-T-C

38427986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7270850-G-A

38428001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7270824-T-C

38428222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7270628-G-A

38428267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7270579-T-C

38428736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7270119-A-G

38428800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7270050-T-C

38429163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7269653-C-T

38429426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7269382-C-T

38429535-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7269273-T-G

38429675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7269131-A-G

38430907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7267594-G-A

38431027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7267470-A-G

38431031-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7267466-T-G

38431118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7267384-G-A

38431217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: missense variant
orthologous variants: 7267287-C-T

38431328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7267175-G-A

38431328-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7267175-G-C

38431698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7266240-A-G

38431741-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7266197-T-G

38431778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7266156-T-C

38431886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7266050-G-A

38431945-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7266006-T-G

38431947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7266004-T-C

38432037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7265935-T-C

38432038-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7265934-A-T

38433812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7265643-G-A

38433860-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7265595-C-G

38433988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7265452-G-A

http://identifiers.org/hco/5/GRCh38#38434026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7265418-C-A

http://identifiers.org/hco/5/GRCh38#38434636-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7264207-A-C

38434843-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7264019-T-A

38434961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7263911-G-A

38434961-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7263911-G-C

http://identifiers.org/hco/5/GRCh38#38435015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7263857-C-A

38435015-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7263857-C-G

38435015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7263857-C-T

38435280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7263638-C-T

38435331-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7263599-T-A

http://identifiers.org/hco/5/GRCh38#38435335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7263595-C-A

38435335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7263595-C-T

38435371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7263559-A-G

38435376-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7263554-T-A

38435377-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7263553-A-T

http://identifiers.org/hco/5/GRCh38#38435403-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7263526-C-A

38435403-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7263526-C-G

38435454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7263490-C-T

38435542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7263404-T-C

38435587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7263359-G-T

38435732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7263217-A-G

38436271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7263004-G-T

38436337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7262940-G-A

38436396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7262859-C-T

38436551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7262698-G-A

38436583-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7262685-T-A

38436726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7262542-C-T

38436827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7262440-A-G

38436864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7262410-C-T

38437216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7262051-T-C

38437291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7261985-A-G

38437731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7261713-C-T

38437812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7261657-T-C

http://identifiers.org/hco/5/GRCh38#38438189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7261315-C-A

38438189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7261315-C-T

38438268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 7261254-T-C

38438308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: missense variant
orthologous variants: 7261214-C-T

http://identifiers.org/hco/5/GRCh38#38438338-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7261184-A-C

38438360-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: missense variant
orthologous variants: 7261162-G-C

http://identifiers.org/hco/5/GRCh38#38438402-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7261120-A-C

38438480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7261044-G-A

38438480-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7261044-G-C

38438480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7261044-G-T

38438516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7260762-T-C

http://identifiers.org/hco/5/GRCh38#38438550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7260726-C-A

38438564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7260712-T-C

38438564-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7260712-T-G

38438566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7260710-G-A

38438566-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7260710-G-C

38438591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7260675-A-G

38438597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7260660-T-C

38439055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7260252-A-G

38439228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7260106-A-G

38439333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7259986-C-T

http://identifiers.org/hco/5/GRCh38#38439423-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7259913-A-C

38439640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7259704-G-T

38439667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7259666-C-T

38439721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7259630-A-G

38440334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7258664-A-G

38440335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7258663-T-C

38440483-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7258519-T-G

38440551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7258454-G-A

38440551-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7258454-G-C

38440580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7258420-A-G

38440610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7258389-G-A

38440610-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7258389-G-C

38441969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7255878-T-C

38441974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7255873-C-T

38442008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7255838-C-T

38442024-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, undefined
orthologous variants: 7255823-C-G

38442062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, undefined
orthologous variants: 7255785-G-A

38442093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, undefined
orthologous variants: 7255753-C-T

http://identifiers.org/hco/5/GRCh38#38445016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7254681-C-A

http://identifiers.org/hco/5/GRCh38#38445332-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7254427-A-C

38445332-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7254427-A-T

http://identifiers.org/hco/5/GRCh38#38445477-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7254323-A-C

38445477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7254323-A-G

38445477-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7254323-A-T

http://identifiers.org/hco/5/GRCh38#38445509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7254291-C-A

38445511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7254289-G-A

38445511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7254289-G-T

38445748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7254047-T-C

38445786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7254008-G-A

38445786-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7254008-G-C

38445786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7254008-G-T

38445894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7253884-C-T

38446023-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7253740-G-C

38447289-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7252949-G-C

38448114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7252499-G-A

38448114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7252499-G-T

http://identifiers.org/hco/5/GRCh38#38448315-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7252291-A-C

38448315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 7252291-A-G

38448430-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7252177-C-G

38448502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7252113-G-A

38448502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7252113-G-T

38448503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7252112-G-A

38448503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7252112-G-T

38448510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7252105-G-A

38448510-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7252105-G-C

http://identifiers.org/hco/5/GRCh38#38448531-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7252089-A-C

38448605-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7252021-C-G

38448671-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7251958-A-T

38448675-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7251954-T-A

38448750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7251865-C-T

38448844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7251747-A-G

38448853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7251738-C-T

38448903-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7251700-C-G

38448903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7251700-C-T

38448971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7251604-G-A

38449361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7251160-T-C

38449387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7251134-T-C

http://identifiers.org/hco/5/GRCh38#38449433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7251094-C-A

38449433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7251094-C-T

38449434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7251093-C-T

38449463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7251064-A-G

http://identifiers.org/hco/5/GRCh38#38449626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7250889-C-A

38449694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7250849-A-G

38449745-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7250809-G-C

38450374-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7250276-A-T

38450496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7250146-C-T

38450508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7250134-T-C

38451404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 7249158-G-A

38451404-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 7249158-G-C

38451561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7248984-G-A

http://identifiers.org/hco/5/GRCh38#38451617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7248929-C-A

38452947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7247400-C-T

38453005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7247367-G-A

38453184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7247262-C-T

38453210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7247223-G-T

38453439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7246972-G-A

38453439-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7246972-G-C

38453476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7246935-C-T

38453497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, undefined
orthologous variants: 7246934-A-G

38453769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, undefined
orthologous variants: 7246644-C-T

http://identifiers.org/hco/5/GRCh38#38453955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#7246462-C-A

38453955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, undefined
orthologous variants: 7246462-C-T

38454191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7246259-C-T

38454393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7245979-G-T

38454423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7245949-T-C

38454699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7245636-G-A

38454960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7245373-G-A

38454982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7245351-G-A

38454993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7245339-G-A

38455556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7244903-G-A

38455671-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7244787-T-G

38455862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7244606-A-G

38455862-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7244606-A-T

38456103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7244412-A-G

38456237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7244299-C-T

38456689-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7243484-C-G

38456831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7243396-G-A

38456929-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7243304-C-G

38457366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7242533-G-A

38457857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7242111-A-G

38457866-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7242102-C-G

38458138-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7241861-T-A

http://identifiers.org/hco/5/GRCh38#38458203-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7241794-A-C

38458203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7241794-A-G

38458203-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7241794-A-T

http://identifiers.org/hco/5/GRCh38#38458240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7241753-C-A

http://identifiers.org/hco/5/GRCh38#38458256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7241739-C-A

38458267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7241728-G-A

38458366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: missense variant
orthologous variants: 7241638-G-A

38458366-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: missense variant
orthologous variants: 7241638-G-C

38458453-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7241556-T-A

http://identifiers.org/hco/5/GRCh38#38458455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7241554-C-A

38459784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7240095-G-A

http://identifiers.org/hco/5/GRCh38#38459966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7239907-C-A

38460212-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7239675-C-G

38460212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7239675-C-T

38460234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7239653-G-A

38460269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7239621-T-C

38460424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7239482-A-G

38460486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7239423-G-T

38460501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7239408-G-A

38460561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7239354-G-T

38460674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7239244-G-A

38460778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7239153-T-C

http://identifiers.org/hco/5/GRCh38#38460797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7239136-C-A

38460807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7239126-G-A

38460858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7239069-G-A

38460869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron variant
orthologous variants: 7239058-G-T

38461057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7238855-A-G

38461525-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7238476-T-A

38461525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7238476-T-C

http://identifiers.org/hco/5/GRCh38#38461532-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7238469-A-C

38462759-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7238210-T-G

38462810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7238177-G-A

38462810-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7238177-G-C

38462814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7238173-G-A

38462933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7238059-G-A

38462970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7238022-G-A

38462970-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7238022-G-C

38463697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7237390-A-G

38463697-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7237390-A-T

38463746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7237362-T-C

http://identifiers.org/hco/5/GRCh38#38464115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7236997-C-A

http://identifiers.org/hco/5/GRCh38#38464184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#7236936-C-A

38464184-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 7236936-C-G

38464235-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 7236885-T-A

http://identifiers.org/hco/5/GRCh38#38464258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#7236862-C-A

38464258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 7236862-C-T

38464437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 7236637-T-C

38464487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 7236587-C-T

38464590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7236483-T-C

38464636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7236433-A-G

38464694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7236374-A-G

38464884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7236180-G-T

38465082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7235999-A-G

38465087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7235994-C-T

38465114-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7235967-T-A

38465122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7235960-G-T

http://identifiers.org/hco/5/GRCh38#38465149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#7235933-C-A

38465152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7235930-A-G

38465418-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26810
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7235669-G-T