65169882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 120814959-G-A

65170041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120814797-A-G

http://identifiers.org/hco/12/GRCh38#65170113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#120814722-C-A

65170113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120814722-C-T

65170218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 120814617-C-T

65170313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 120814519-G-A

65170321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120814511-G-A

65170321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120814511-G-T

65170386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120814443-G-A

65170504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 120814310-G-A

65170671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 120814134-G-A

65170698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 120814107-C-T

http://identifiers.org/hco/12/GRCh38#65170704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#120814101-C-A

http://identifiers.org/hco/12/GRCh38#65171132-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#120813644-C-A

65171132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120813644-C-T

65171145-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120813631-T-G

65171149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120813627-A-G

http://identifiers.org/hco/12/GRCh38#65171323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#120813471-C-A

65171323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120813471-C-T

65171447-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 120813361-C-G

65171447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 120813361-C-T

65171585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120813243-G-A

http://identifiers.org/hco/12/GRCh38#65171649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#120813195-C-A

65171649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120813195-C-T

65171715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120813141-T-C

65171733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120813123-G-T

http://identifiers.org/hco/12/GRCh38#65172258-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#120812784-A-C

65172418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120812399-A-G

http://identifiers.org/hco/12/GRCh38#65172488-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#120812324-A-C

65172601-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120812221-A-T

65173190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120810676-C-T

http://identifiers.org/hco/12/GRCh38#65173299-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#120810576-A-C

65173299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120810576-A-G

65173507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120810311-G-A

65173775-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120809990-T-G

65173787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120809978-A-G

65173970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120809838-C-T

65174133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120809697-A-G

65174482-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120809266-T-G

65174531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120809217-A-G

65174713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120809041-G-A

65174713-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120809041-G-C

65174892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120808929-A-G

65174990-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120808847-G-C

http://identifiers.org/hco/12/GRCh38#65175182-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#120808769-A-C

65175234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120808711-G-A

65175407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120808526-C-T

65175421-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120808493-T-G

http://identifiers.org/hco/12/GRCh38#65175463-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#120808450-A-C

65175501-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120808410-C-G

65175540-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120808372-T-G

65175555-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120808360-C-G

http://identifiers.org/hco/12/GRCh38#65175655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#120808273-C-A

65175934-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120808025-T-G

65175974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120807990-C-T

65176164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120807644-A-G

65176568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120807316-A-G

65176568-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120807316-A-T

65176846-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120807043-C-G

65176846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120807043-C-T

65176856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120807033-C-T

65176867-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120807022-T-G

65176935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120806880-A-G

http://identifiers.org/hco/12/GRCh38#65177231-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#120806510-A-C

65177231-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120806510-A-T

65177264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120806475-G-A

65177457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120806283-A-G

65177576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120806172-T-C

65177763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120806029-A-G

65178510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120805544-A-G

65178593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120805467-C-T

65178694-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120805377-A-T

65178706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120805372-A-G

65178890-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120805181-G-C

65179018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120804874-G-A

65182164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120803337-A-G

65182184-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120803321-A-T

65182286-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120803232-A-T

65182517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120803014-T-C

65182531-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120802995-A-T

65182609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120802916-A-G

http://identifiers.org/hco/12/GRCh38#65182874-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#120802070-A-C

65182885-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120802062-T-G

65187132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120799339-A-G

65187132-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120799339-A-T

65187135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120799336-A-G

65187240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120799252-T-C

65205682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120793983-G-A

65205682-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120793983-G-C

65205748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120793927-C-T

65205756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120793921-G-A

65205824-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120793853-G-C

65206032-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120793707-T-A

65206121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120793491-G-A

65206231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120793393-A-G

http://identifiers.org/hco/12/GRCh38#65206405-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#120793020-A-C

65206405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120793020-A-G

65206563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120792885-T-C

65207007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120792502-T-C

65207027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120792475-A-G

65207261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120792275-G-A

65207402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120792181-A-G

65207457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120792128-A-G

65208314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120790347-G-A

65208530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120790041-A-G

65209247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120789429-G-A

65209838-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120789104-G-C

65210058-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120788919-T-G

65210723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120788351-A-G

65210787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120788293-A-G

65210819-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120788265-T-G

65210847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120788237-T-C

65210858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120788226-A-G

65210866-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120788218-T-G

65211324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: 120787867-T-C

65211423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: 120787774-A-G

http://identifiers.org/hco/12/GRCh38#65214354-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#120787029-A-C

65214659-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: 120786742-T-G

65214705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: 120786692-G-A

65214708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: 120786689-C-T

65214726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: 120786671-T-C

65215580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: 120785978-G-A

65215580-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: 120785978-G-T

65215611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: 120785910-C-T

65215694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: 120785669-G-A

http://identifiers.org/hco/12/GRCh38#65215833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#120785391-C-A

65215833-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: 120785391-C-G

http://identifiers.org/hco/12/GRCh38#65215936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#120785306-C-A

65215936-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: 120785306-C-G

65215936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: 120785306-C-T

http://identifiers.org/hco/12/GRCh38#65216016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#120785227-C-A

65216016-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: missense variant
orthologous variants: 120785227-C-G

65216060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: 120785184-T-C

65216405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: 120784922-G-A

65216648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: 120784692-A-G

65216648-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: 120784692-A-T

65216668-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: 120784671-T-G

65216906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: 120784422-G-A

65217044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: 120784297-C-T

http://identifiers.org/hco/12/GRCh38#65217100-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#120784246-A-C

65217148-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: 120784199-G-C

65218095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: 120783503-T-C

65218428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: 120783284-T-C

65218519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: 120783204-G-A

65218519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: 120783204-G-T

65218554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 120783172-G-A

65218647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: 120783079-G-A

65218647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: 120783079-G-T

65226625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: 120776352-T-C

65226625-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: 120776352-T-G

65226670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: 120776306-A-G

65232566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: 120774564-A-G

65232913-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: 120774295-A-T

65233017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: 120774029-G-A

65233169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: 120773828-A-G

65233171-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: 120773826-C-G

65233227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: 120773776-T-C

65235966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: 120772765-T-C

http://identifiers.org/hco/12/GRCh38#65236082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#120772645-C-A

65236082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: 120772645-C-T

65236084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: 120772643-A-G

65236112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: 120772620-G-A

65237643-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: 120770147-C-G

65237870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: 120769937-A-G

65238313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: 120769776-A-G

http://identifiers.org/hco/12/GRCh38#65238362-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#120769727-C-A

65238362-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: 120769727-C-G

65238362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: 120769727-C-T

65238439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: 120769661-G-A

65238439-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: 120769661-G-C

65238439-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: 120769661-G-T

65238447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: 120769653-A-G

65238447-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: 120769653-A-T

65238847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: 120769265-G-A

65238904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: 120769214-T-C

65238908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: 120769210-G-A

65238908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: 120769210-G-T

65238909-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: 120769209-G-C

http://identifiers.org/hco/12/GRCh38#65238941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#120769177-C-A

65238941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: 120769177-C-T

65239985-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: missense variant
orthologous variants: 120767876-G-C

65240036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: 120767825-A-G

65240046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: 120767815-G-A

65240046-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: 120767815-G-C

65240319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: 120767553-G-T

65240441-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: 120767465-T-A

65240444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: 120767462-T-C

65240518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: 120767397-G-T

65240538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: 120767378-C-T

65240560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron variant
orthologous variants: 120767359-T-C

65240587-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120767336-A-T

http://identifiers.org/hco/12/GRCh38#65240731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#120767246-C-A

65240731-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120767246-C-G

65240843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120767184-T-C

65241192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120766839-C-T

http://identifiers.org/hco/12/GRCh38#65241202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#120766826-C-A

65241202-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120766826-C-G

65241202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120766826-C-T

http://identifiers.org/hco/12/GRCh38#65241208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#120766820-C-A

65241208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120766820-C-T

65241620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120766418-G-A

65241620-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120766418-G-C

65241676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120766362-C-T

65241707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120766315-A-G

65241709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120766313-A-G

65242052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120766049-A-G

65242165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120765940-T-C

65242295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120765796-A-G

65242427-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120765718-T-A

65242557-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120765577-C-G

65242681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120765519-T-C

65242829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120765392-C-T

65242878-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120765341-G-C

65243111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120765086-T-C

65243512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120763805-T-C

http://identifiers.org/hco/12/GRCh38#65243519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#120763798-C-A

65243600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120763740-A-G

http://identifiers.org/hco/12/GRCh38#65245656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#120761955-C-A

65245779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120761833-A-G

65245788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120761824-T-C

65246410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120761214-T-C

65246497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120761125-G-A

http://identifiers.org/hco/12/GRCh38#65246498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#120761124-C-A

65246516-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120761105-T-G

65246604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: 3 prime UTR variant
orthologous variants: 120761026-T-C

65246615-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: 3 prime UTR variant
orthologous variants: 120761015-T-G

http://identifiers.org/hco/12/GRCh38#65247099-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#120760517-A-C

65247466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28887
most severe consequence: 3 prime UTR variant
orthologous variants: 120760159-A-G