52218904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: non coding transcript exon variant
orthologous variants: 22862191-G-A

52219482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: non coding transcript exon variant
orthologous variants: 22861273-G-A

52219635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 22861148-G-A

52219635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 22861148-G-T

52219742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22861057-C-T

http://identifiers.org/hco/13/GRCh38#52219755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#22861043-C-A

52219756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22861042-T-C

52219777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22861005-G-A

52219777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22861005-G-T

52219796-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22860986-T-A

52220248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22860738-T-C

52220313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22860675-G-A

http://identifiers.org/hco/13/GRCh38#52221195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#22860298-C-A

52221203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22860290-A-G

http://identifiers.org/hco/13/GRCh38#52221231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#22860252-C-A

52221231-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22860252-C-G

52221297-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22860189-A-T

52221618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22859698-A-G

http://identifiers.org/hco/13/GRCh38#52221645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#22859674-C-A

52221645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22859674-C-T

52221824-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22859495-T-A

52221876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22859443-G-A

http://identifiers.org/hco/13/GRCh38#52221924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#22859400-C-A

52221958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22859366-C-T

52223201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22856050-A-G

http://identifiers.org/hco/13/GRCh38#52223202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#22856049-C-A

52223202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22856049-C-T

52223206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22856045-A-G

52223252-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: non coding transcript exon variant
orthologous variants: 22856007-T-A

52223252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: non coding transcript exon variant
orthologous variants: 22856007-T-C

52223252-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: non coding transcript exon variant
orthologous variants: 22856007-T-G

52223276-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: non coding transcript exon variant
orthologous variants: 22855983-G-C

52223276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: non coding transcript exon variant
orthologous variants: 22855983-G-T

http://identifiers.org/hco/13/GRCh38#52223282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#22855977-C-A

52223282-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: non coding transcript exon variant
orthologous variants: 22855977-C-G

52223282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: non coding transcript exon variant
orthologous variants: 22855977-C-T

http://identifiers.org/hco/13/GRCh38#52223389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#22855865-C-A

52223389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22855865-C-T

52225659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22851236-G-A

52225679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22851216-T-C

http://identifiers.org/hco/13/GRCh38#52225703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#22851192-C-A

52225744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22851153-T-C

52225746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22851151-T-C

52225816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22851096-G-A

52225838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22851084-C-T

52225949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22850985-T-C

52225993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22850948-C-T

52226028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22850922-T-C

52226102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22850844-T-C

52226102-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22850844-T-G

52226173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22850756-G-A

52226394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22850407-A-G

52226511-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22850296-C-G

52226511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22850296-C-T

52226662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22850147-A-G

52226824-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22849995-G-C

http://identifiers.org/hco/13/GRCh38#52226973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#22849531-C-A

52226973-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22849531-C-G

52227013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: non coding transcript exon variant
orthologous variants: 22849492-T-C

52227024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: non coding transcript exon variant
orthologous variants: 22849484-G-A

52227024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: non coding transcript exon variant
orthologous variants: 22849484-G-T

52227025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: non coding transcript exon variant
orthologous variants: 22849483-T-C

52227066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: non coding transcript exon variant
orthologous variants: 22849439-T-C

52227141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22849368-A-G

http://identifiers.org/hco/13/GRCh38#52227149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#22849360-C-A

52227149-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22849360-C-G

52227149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22849360-C-T

52227454-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22849197-T-G

52227465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22849186-G-A

52227465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22849186-G-T

52227784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22848971-T-C

52227830-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22848928-C-G

52227830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22848928-C-T

52227868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22848892-A-G

52227880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22848880-G-A

52229468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22845443-G-A

52229468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22845443-G-T

http://identifiers.org/hco/13/GRCh38#52229492-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#22845419-A-C

52229492-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22845419-A-T

52232434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22842529-G-A

52232434-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22842529-G-C

52232954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22841619-T-C

52232984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22841585-T-C

52233046-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22841556-C-G

52233116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22841485-C-T

52234602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22840116-T-C

52234661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22840048-C-T

52234811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22839782-T-C

52234848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22839744-C-T

52234914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22839683-T-C

52234927-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22839669-A-T

52234972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22839623-T-C

http://identifiers.org/hco/13/GRCh38#52234986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#22839609-C-A

52234986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22839609-C-T

52235299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22839318-G-A

52235299-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22839318-G-C

52253254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22838164-A-G

52253283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22838150-T-C

52253315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22838118-G-A

http://identifiers.org/hco/13/GRCh38#52253475-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#22837975-A-C

52253523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22837927-T-C

http://identifiers.org/hco/13/GRCh38#52254041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#22835810-C-A

52254068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22835783-A-G

52254069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22835782-A-G

52254131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22835724-A-G

52258144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22835429-G-A

52258144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22835429-G-T

52258340-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22835234-G-C

52258357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22835217-G-A

52258397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22835178-G-A

52258472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22835109-T-C

52258491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22835097-T-C

52258515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22835073-A-G

52258660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22834926-A-G

http://identifiers.org/hco/13/GRCh38#52258683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#22834906-C-A

52258706-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22834882-T-A

52258706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22834882-T-C

http://identifiers.org/hco/13/GRCh38#52258715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#22834873-C-A

52261565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22829576-C-T

52261613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22829538-T-C

52261639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22829511-T-C

52261672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22829478-T-C

52261749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22829402-T-C

52261790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22829361-T-C

52261806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22828990-T-C

52261912-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22827896-G-C

52261958-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22827850-T-A

52261960-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22827848-G-C

http://identifiers.org/hco/13/GRCh38#52261972-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#22827835-A-C

52261972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22827835-A-G

52262079-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22827758-C-G

52262368-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22827560-G-C

http://identifiers.org/hco/13/GRCh38#52279711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#22826693-C-A

52279867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: non coding transcript exon variant
orthologous variants: 22826547-G-A

52279867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: non coding transcript exon variant
orthologous variants: 22826547-G-T

52279911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 22826503-A-G

52279937-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22826477-T-A

52280080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22826332-A-G

52280129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22826284-A-G

52280157-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22826256-C-G

52280255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22826076-C-T

52280428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22825897-T-C

52280592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22825751-A-G

52280593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22825750-T-C

52280633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22825709-A-G

52280646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22825696-A-G

52280672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: non coding transcript exon variant
orthologous variants: 22825670-A-G

52280675-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: non coding transcript exon variant
orthologous variants: 22825667-T-A

52280675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: non coding transcript exon variant
orthologous variants: 22825667-T-C

52280693-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: non coding transcript exon variant
orthologous variants: 22825649-T-A

http://identifiers.org/hco/13/GRCh38#52280699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#22825643-C-A

52280699-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: non coding transcript exon variant
orthologous variants: 22825643-C-G

52280711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: non coding transcript exon variant
orthologous variants: 22825631-G-T

http://identifiers.org/hco/13/GRCh38#52280944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#22825390-C-A

52280944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: non coding transcript exon variant
orthologous variants: 22825390-C-T

52281294-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22824746-T-G

52281512-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22824546-C-G

52281578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22824480-A-G

52281578-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22824480-A-T

http://identifiers.org/hco/13/GRCh38#52281797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#22824111-C-A

52281806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22824102-T-C

52281844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22824064-G-A

52281844-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22824064-G-C

52281917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22823998-C-T

52282786-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22823712-G-C

52282987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22823602-C-T

52283059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22823535-G-A

http://identifiers.org/hco/13/GRCh38#52283101-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#22823483-A-C

52283101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22823483-A-G

52283133-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22823451-T-A

52283226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22823310-T-C

52283346-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: non coding transcript exon variant
orthologous variants: 22823190-T-A

52283346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: non coding transcript exon variant
orthologous variants: 22823190-T-C

52289777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22817867-A-G

52289836-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: non coding transcript exon variant
orthologous variants: 22817805-T-A

52289836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: non coding transcript exon variant
orthologous variants: 22817805-T-C

52289845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: non coding transcript exon variant
orthologous variants: 22817796-A-G

52289845-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: non coding transcript exon variant
orthologous variants: 22817796-A-T

52289870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: non coding transcript exon variant
orthologous variants: 22817771-A-G

52289870-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: non coding transcript exon variant
orthologous variants: 22817771-A-T

52290075-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22817598-A-T

http://identifiers.org/hco/13/GRCh38#52290355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#22817318-C-A

http://identifiers.org/hco/13/GRCh38#52290418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#22817257-C-A

http://identifiers.org/hco/13/GRCh38#52290421-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#22817254-A-C

52290484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22816980-G-A

52290484-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22816980-G-C

52290517-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22816932-T-A

52290517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22816932-T-C

52290564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22816885-T-C

52290679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22816763-G-A

http://identifiers.org/hco/13/GRCh38#52290960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#22815798-C-A

52291033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22815723-T-C

52291050-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22815705-G-C

52291050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22815705-G-T

52291080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22815672-G-A

52291465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22815602-T-C

52291516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: non coding transcript exon variant
orthologous variants: 22815551-A-G

52291516-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: non coding transcript exon variant
orthologous variants: 22815551-A-T

http://identifiers.org/hco/13/GRCh38#52291587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#22815481-C-A

52291617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22815448-A-G

52291754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22815327-G-A

52291803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22815278-A-G

52291867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22815219-T-C

http://identifiers.org/hco/13/GRCh38#52291918-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#22815169-C-A

52296812-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22812606-A-T

http://identifiers.org/hco/13/GRCh38#52297028-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#22812378-C-A

52297141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22812268-G-A

http://identifiers.org/hco/13/GRCh38#52297203-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#22812226-A-C

52297511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22811971-C-T

http://identifiers.org/hco/13/GRCh38#52297689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#22811845-C-A

52297711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22811823-T-C

http://identifiers.org/hco/13/GRCh38#52308225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#22795929-C-A