90963793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: 3 prime UTR variant
orthologous variants: 97517466-T-C

http://identifiers.org/hco/12/GRCh38#90963927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97517352-C-A

90963927-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: 3 prime UTR variant
orthologous variants: 97517352-C-G

90963993-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: 3 prime UTR variant
orthologous variants: 97517300-T-A

90963993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: 3 prime UTR variant
orthologous variants: 97517300-T-C

90963993-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: 3 prime UTR variant
orthologous variants: 97517300-T-G

90964005-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: 3 prime UTR variant
orthologous variants: 97517288-T-A

90964005-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: 3 prime UTR variant
orthologous variants: 97517288-T-G

90964019-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: 3 prime UTR variant
orthologous variants: 97517269-T-A

90964041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: 3 prime UTR variant
orthologous variants: 97517246-T-C

90964103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: 3 prime UTR variant
orthologous variants: 97517191-A-G

90964148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: 3 prime UTR variant
orthologous variants: 97517146-A-G

90964148-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: 3 prime UTR variant
orthologous variants: 97517146-A-T

90964196-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: missense variant
orthologous variants: 97517090-T-A

90964258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: synonymous variant
orthologous variants: 97517028-C-T

90964286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: missense variant
orthologous variants: 97517000-T-C

90964386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: 97516898-G-T

90964423-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: 97516863-T-A

90964423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: 97516863-T-C

90964423-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: 97516863-T-G

http://identifiers.org/hco/12/GRCh38#90964477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97516800-C-A

90965160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: 97516281-C-T

90965295-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: 97516142-T-G

90965300-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: 97516137-T-G

90965423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: 97516014-G-A

90965429-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: 97516008-T-A

90965499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: 97515946-T-C

90965514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: 97515931-A-G

90965638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: 97515775-T-C

90965652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: 97515761-T-C

90965654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: 97515759-A-G

90965654-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: 97515759-A-T

90965705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: 97515709-G-A

90965726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: 97515688-A-G

http://identifiers.org/hco/12/GRCh38#90965806-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97515605-A-C

90965806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: 97515605-A-G

90965917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: 97515440-T-C

90966294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: 97514905-G-T

90969118-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: 97513813-C-G

90969379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: 97513601-T-C

90969551-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: 97513402-A-T

90969955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: 97513031-C-T

90969957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: 97513029-A-G

90969974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: 97513012-G-T

90970024-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: 97512963-C-G

http://identifiers.org/hco/12/GRCh38#90970087-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97512900-A-C

90970087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: missense variant
orthologous variants: 97512900-A-G

90970087-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: missense variant
orthologous variants: 97512900-A-T

90970238-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: 97512804-A-T

90970250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: 97512793-T-C

http://identifiers.org/hco/12/GRCh38#90970253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97512790-C-A

90970253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: 97512790-C-T

90970254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: 97512789-A-G

90970376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: 97512694-G-T

90970402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: 97512667-A-G

90970920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: 97512212-A-G

90970920-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: 97512212-A-T

90970960-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: 97512171-A-T

90971049-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: 97512083-T-A

http://identifiers.org/hco/12/GRCh38#90971095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97512052-C-A

90971231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: 97511941-A-G

90971731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: 97511783-A-G

90971737-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: 97511777-G-T

90971742-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: 97511770-T-A

http://identifiers.org/hco/12/GRCh38#90971743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97511769-C-A

http://identifiers.org/hco/12/GRCh38#90971784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97511724-C-A

90971784-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: 97511724-C-G

90971960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: missense variant
orthologous variants: 97511548-T-C

90972039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: 97511463-T-C

90972176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: 97511334-A-G

90972402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: 97511100-G-T

90972414-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: 97511088-A-T

90972425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: 97511078-T-C

90972508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: 97510993-A-G

90972535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: 97510968-A-G

http://identifiers.org/hco/12/GRCh38#90972611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97510895-C-A

90972611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97510895-C-T

90972612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97510894-A-G

90972631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97510875-G-A

90972631-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97510875-G-C

90972631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97510875-G-T

90972757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97510753-T-C

90972775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97510735-A-G

90972778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97510732-G-A

90972778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97510732-G-T

90972782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97510728-T-C

90972782-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97510728-T-G

90972784-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97510726-T-A

90972882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 97510635-A-G

90973006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97510511-A-G

90973008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97510509-A-G

90973008-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97510509-A-T

90973052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97510471-G-T

http://identifiers.org/hco/12/GRCh38#90973074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97510445-C-A

90973122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97510397-G-T

90973172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97510330-T-C

90973178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97510324-G-A

90973239-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97510282-T-G

90973528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97510029-T-C

90973558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97509998-C-T

90973562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97509994-G-A

90973587-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97509969-C-G

90973606-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97509949-G-C

90975157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97509813-G-T

90975228-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97509746-T-A

90975257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97509720-T-C

http://identifiers.org/hco/12/GRCh38#90975335-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97509645-A-C

90975340-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97509640-T-G

90977508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97507798-T-C

90977510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97507796-G-A

90977510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97507796-G-T

90977775-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97507565-C-G

90977928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97507406-A-G

http://identifiers.org/hco/12/GRCh38#90977961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97507371-C-A

90977961-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97507371-C-G

http://identifiers.org/hco/12/GRCh38#90978027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97506594-C-A

90978061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97506559-T-C

90978213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 97506407-G-A

90978218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97506402-G-A

90978218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97506402-G-T

90978264-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 97506356-T-A

90978264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 97506356-T-C

90978264-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 97506356-T-G

90978387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97506246-T-C

90978402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97506223-G-A

90978402-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97506223-G-C

90978402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97506223-G-T

90978730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97505925-T-C

90978849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97505813-G-A

90978869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97505792-A-G

90979062-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97505608-G-C

90979647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97505139-A-G

90979673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97505115-G-T

http://identifiers.org/hco/12/GRCh38#90979877-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97504916-A-C

90980313-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97504504-G-C

90980368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97504463-A-G

90980426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97504415-C-T

90980495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97504340-A-G

http://identifiers.org/hco/12/GRCh38#90980527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97504304-C-A

90980648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97504190-T-C

90980738-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97504114-T-G

90980979-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97503898-A-T

90981292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97503575-G-A

90981302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97503567-G-A

90981386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97503487-T-C

90981398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97503475-G-T

90981506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97503366-A-G

90981506-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97503366-A-T

90981683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97503191-G-A

90992404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97494535-A-G

90992441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97494498-G-T

90992529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97494402-T-C

90992545-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97494386-T-G

90992599-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97494332-T-G

90992629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97494302-T-C

http://identifiers.org/hco/12/GRCh38#90993855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97493922-C-A

90993855-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97493922-C-G

90993855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97493922-C-T

http://identifiers.org/hco/12/GRCh38#90994231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97493658-C-A

90994231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97493658-C-T

90994242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97493648-C-T

90994458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97493448-A-G

90994519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97493394-A-G

http://identifiers.org/hco/12/GRCh38#90994760-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97493188-A-C

90994760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97493188-A-G

90994974-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97492984-A-T

90995065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97492895-A-G

http://identifiers.org/hco/12/GRCh38#90995278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97492695-C-A

90995333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97492637-T-C

90995726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97492267-C-T

90996001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97491993-T-C

90996246-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97491428-A-T

http://identifiers.org/hco/12/GRCh38#90996296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97491385-C-A

90996296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97491385-C-T

91000437-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97487193-G-C

91000476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97487154-C-T

http://identifiers.org/hco/12/GRCh38#91000534-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97487097-C-A

91000679-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97486954-G-C

91000683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97486950-T-C

91000724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97486894-G-T

91001088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97486815-G-A

91001118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97486785-G-A

91001118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97486785-G-T

91001246-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97486692-T-G

91001250-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97486688-A-T

91001797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97486192-T-C

91001797-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97486192-T-G

91001814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97486176-T-C

91001822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97486168-C-T

http://identifiers.org/hco/12/GRCh38#91002321-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97485802-A-C

91002341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97485782-G-T

91002366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97485757-C-T

91002444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 97485681-T-C

91002540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: missense variant
orthologous variants: 97485585-A-G

91002540-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: missense variant
orthologous variants: 97485585-A-T

http://identifiers.org/hco/12/GRCh38#91002590-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97485535-A-C

91002590-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: 97485535-A-T

91002650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: 97485481-G-T

91002719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: 97485415-A-G

http://identifiers.org/hco/12/GRCh38#91002724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97485410-C-A

91002724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: 97485410-C-T

http://identifiers.org/hco/12/GRCh38#91002726-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97485408-A-C

http://identifiers.org/hco/12/GRCh38#91002727-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97485407-A-C

91002877-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: 97485250-T-A

91003065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: 97485118-C-T

91003070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: 97485113-A-G

91003300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: 97484932-A-G

91003378-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: 97484860-C-G

91003688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: 97484529-A-G

91003766-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: 97484463-C-G

91003908-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: 97484347-G-C

http://identifiers.org/hco/12/GRCh38#91004023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97484232-C-A

91004032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: 97484224-A-G

91004044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: 97484212-G-T

91004115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: 97484142-A-G

91004557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: 97483707-T-C

http://identifiers.org/hco/12/GRCh38#91004843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97483422-C-A

91004843-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: 97483422-C-G

http://identifiers.org/hco/12/GRCh38#91004850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97483412-C-A

91004850-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: 97483412-C-G

http://identifiers.org/hco/12/GRCh38#91004853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97483409-C-A

91004904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3053
most severe consequence: intron variant
orthologous variants: 97483355-G-T