58515406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: non coding transcript exon variant
orthologous variants: 173689962-G-A

58515406-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: non coding transcript exon variant
orthologous variants: 173689962-G-C

58515406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: non coding transcript exon variant
orthologous variants: 173689962-G-T

58515417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: non coding transcript exon variant
orthologous variants: 173689973-T-C

58515417-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: non coding transcript exon variant
orthologous variants: 173689973-T-G

http://identifiers.org/hco/20/GRCh38#58515447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173689987-C-A

58515447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: non coding transcript exon variant
orthologous variants: 173689987-C-T

58515453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: non coding transcript exon variant
orthologous variants: 173689993-T-C

http://identifiers.org/hco/20/GRCh38#58515468-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173690006-A-C

58515468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: non coding transcript exon variant
orthologous variants: 173690006-A-G

58515468-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: non coding transcript exon variant
orthologous variants: 173690006-A-T

58515482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: non coding transcript exon variant
orthologous variants: 173690020-G-A

58515482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: non coding transcript exon variant
orthologous variants: 173690020-G-T

58515489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: non coding transcript exon variant
orthologous variants: 173690027-G-A

58515489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: non coding transcript exon variant
orthologous variants: 173690027-G-T

http://identifiers.org/hco/20/GRCh38#58515504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173690041-C-A

58515504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: non coding transcript exon variant
orthologous variants: 173690041-C-T

58515512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: non coding transcript exon variant
orthologous variants: 173690049-C-T

58515543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: non coding transcript exon variant
orthologous variants: 173690072-A-G

58515546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: non coding transcript exon variant
orthologous variants: 173690075-G-A

58515546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: non coding transcript exon variant
orthologous variants: 173690075-G-T

http://identifiers.org/hco/20/GRCh38#58515560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173690083-C-A

58515560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: non coding transcript exon variant
orthologous variants: 173690083-C-T

58515561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: non coding transcript exon variant
orthologous variants: 173690084-C-T

58515659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: non coding transcript exon variant
orthologous variants: 173690162-G-A

58515659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: non coding transcript exon variant
orthologous variants: 173690162-G-T

http://identifiers.org/hco/20/GRCh38#58515689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173690181-C-A

58515782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173690273-G-A

58515782-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173690273-G-C

58515782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173690273-G-T

http://identifiers.org/hco/20/GRCh38#58515846-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173690332-A-C

58515846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173690332-A-G

58515876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173690362-A-G

58516084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173690549-G-A

58516220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173690635-T-C

58516232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173690647-G-A

58516439-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173690829-G-C

58516451-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173690841-A-T

58516572-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173690912-T-A

58517122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173691125-C-T

58518427-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173692626-T-A

58518528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173692730-G-T

58518532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173692734-T-C

58518844-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173692933-T-G

58519654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173693146-G-A

58519654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173693146-G-T

58519692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173693184-A-G

58519709-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173693202-A-T

58520054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173693534-G-A

58520054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173693534-G-T

58520186-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173693682-T-A

58520251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173693746-G-A

http://identifiers.org/hco/20/GRCh38#58520293-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173693788-A-C

58520293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173693788-A-G

58520317-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173693813-T-A

58520317-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173693813-T-G

58520336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173693833-G-A

58520336-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173693833-G-T

58520409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173693907-A-G

58522278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173694418-C-T

58522440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173694608-C-T

http://identifiers.org/hco/20/GRCh38#58522636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173695486-C-A

58522882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173695825-C-T

http://identifiers.org/hco/20/GRCh38#58522982-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173695905-A-C

58523267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173696190-C-T

http://identifiers.org/hco/20/GRCh38#58523309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173696238-C-A

58523309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173696238-C-T

58523349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173696256-G-A

58523349-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173696256-G-C

58523364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173696271-G-A

58523364-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173696271-G-C

58523379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173696286-G-A

58523379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173696286-G-T

58523387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173696294-G-A

58523387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173696294-G-T

58523625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173696508-G-T

http://identifiers.org/hco/20/GRCh38#58523685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173696584-C-A

58523685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173696584-C-T

http://identifiers.org/hco/20/GRCh38#58523785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173696697-C-A

58523785-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173696697-C-G

58523785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173696697-C-T

58523828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173696741-A-G

58523836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173696749-T-C

http://identifiers.org/hco/20/GRCh38#58523838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173696751-C-A

58523838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173696751-C-T

http://identifiers.org/hco/20/GRCh38#58523908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173696806-C-A

http://identifiers.org/hco/20/GRCh38#58523947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173696833-C-A

58523947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173696833-C-T

58524019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173696903-G-A

58524023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173696907-G-T

58524370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173697296-G-T

http://identifiers.org/hco/20/GRCh38#58524486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173697381-C-A

58524486-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173697381-C-G

58524486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173697381-C-T

http://identifiers.org/hco/20/GRCh38#58524524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173697396-C-A

58524524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173697396-C-T

http://identifiers.org/hco/20/GRCh38#58524581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173697465-C-A

58524586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173697470-A-G

58524586-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173697470-A-T

58524598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173697482-A-G

58524629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 173697514-A-G

58524629-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 173697514-A-T

58524654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173697539-G-A

58524654-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173697539-G-C

http://identifiers.org/hco/20/GRCh38#58524655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173697540-C-A

58524655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173697540-C-T

58524656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173697541-G-A

http://identifiers.org/hco/20/GRCh38#58524671-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173697604-A-C

58524671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173697604-A-G

58524681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173697614-T-C

58524698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173697632-T-C

http://identifiers.org/hco/20/GRCh38#58524746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173697681-C-A

58524796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173697712-T-C

58524808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173697724-C-T

http://identifiers.org/hco/20/GRCh38#58524817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173697735-C-A

58524817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173697735-C-T

58524833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173697751-C-T

58524868-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173697798-T-G

http://identifiers.org/hco/20/GRCh38#58524906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173697838-C-A

58524906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173697838-C-T

58524936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173697868-G-T

58524977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173697887-G-T

58525045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173697939-G-A

58525046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173697940-T-C

http://identifiers.org/hco/20/GRCh38#58525078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173697966-C-A

http://identifiers.org/hco/20/GRCh38#58525093-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173697981-C-A

58525093-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173697981-C-G

58525154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173698029-G-T

http://identifiers.org/hco/20/GRCh38#58525169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173698044-C-A

58525169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173698044-C-T

58525338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173698156-T-C

58525358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173698178-A-G

58525397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173698207-G-A

58525397-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173698207-G-C

58525397-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173698207-G-T

http://identifiers.org/hco/20/GRCh38#58525402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173698212-C-A

58525413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173698223-T-C

http://identifiers.org/hco/20/GRCh38#58525428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173698238-C-A

58525428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173698238-C-T

58525517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173698329-G-T

http://identifiers.org/hco/20/GRCh38#58525526-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173698338-A-C

58525616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173698412-G-A

58525616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173698412-G-T

58525633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173698426-G-A

58525633-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173698426-G-C

58525633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173698426-G-T

http://identifiers.org/hco/20/GRCh38#58525653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173698447-C-A

58525653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173698447-C-T

58525691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173698469-G-A

58525691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173698469-G-T

58525736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173698512-C-T

58525762-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173698540-T-A

58525762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173698540-T-C

58525929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173698662-G-A

58525936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173698669-G-A

58525938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173698671-T-C

58534469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173772968-C-T

http://identifiers.org/hco/20/GRCh38#58534509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173772994-C-A

58534541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173773018-G-A

58534541-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173773018-G-C

58534714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173773165-G-T

58540265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173776942-G-A

58540423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173777100-A-G

58540839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173777194-A-G

http://identifiers.org/hco/20/GRCh38#58540885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173777245-C-A

58540885-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173777245-C-G

http://identifiers.org/hco/20/GRCh38#58541283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173777608-C-A

58543578-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173779573-T-G

http://identifiers.org/hco/20/GRCh38#58543645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173779640-C-A

58543645-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173779640-C-G

58544200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173780098-C-T

58545935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173781528-C-T

58546531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173782043-G-A

58546774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173782235-T-C

http://identifiers.org/hco/20/GRCh38#58546906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173782354-C-A

58546906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173782354-C-T

http://identifiers.org/hco/20/GRCh38#58547105-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173782528-A-C

58547105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173782528-A-G

http://identifiers.org/hco/20/GRCh38#58547488-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173782911-A-C

58547575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173782995-T-C

58547576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173782996-G-A

58547576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173782996-G-T

58547603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173783021-C-T

58547804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 173783222-G-A

58547845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173783262-T-C

58547895-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173783311-G-T

58549424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173785098-G-A

58549630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173785310-A-G

http://identifiers.org/hco/20/GRCh38#58550378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173787171-C-A

58550456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173787254-G-A

58550583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173787375-A-G

58550643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 173787434-A-G

http://identifiers.org/hco/20/GRCh38#58550786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#173787650-C-A

58550786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 173787650-C-T

58550906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173787802-G-A

58550953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 173787827-G-A

58550981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 173787855-G-T

58551065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173787916-G-A

58551065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173787916-G-T

58552911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173789812-G-T

58552919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173789826-G-A

58553598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173790872-G-A

58553598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173790872-G-T

58553991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173791118-G-A

58554033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173791154-G-A

58554130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173791228-G-A

58554312-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173791351-A-T

58554478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173791436-G-A

58554569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173791511-C-T

58554595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173791538-C-T

58554646-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173791588-C-G

58554953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173791846-T-C

58555476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173792371-G-A

58555823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173792683-C-T

58555824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173792684-G-A

58555915-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173792777-T-A

58556429-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173808204-A-T

58556503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173808278-G-T

58557251-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173809318-G-C

58557309-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173809375-A-T

58557322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173809388-G-A

58557564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173809711-G-A

58557601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173809761-T-C

58557679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173809885-G-A

58557937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173810099-C-T

58557945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173810107-C-T

58558466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173810577-G-A

58558799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173810905-G-A

58558807-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173810914-A-T

58558822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 173810937-G-T

58559153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173811222-G-A

58567038-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173814506-T-G

58567092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173814554-T-C

http://identifiers.org/hco/20/GRCh38#58567141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173814597-C-A

58567141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173814597-C-T

58567189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173814645-C-T

58567680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173815011-T-C

58568185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173815617-C-T

58569455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173816901-G-A

58569624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 173817148-A-G

58569643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 173817166-A-G

58570154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173818026-G-A

58570297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173818148-G-A

58570396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173818249-T-C

http://identifiers.org/hco/20/GRCh38#58570525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173818373-C-A

58570525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173818373-C-T

58570744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173818608-C-T

58570991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173818813-G-A

http://identifiers.org/hco/20/GRCh38#58571255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173819182-C-A

58571298-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173819392-G-C

58571298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173819392-G-T

58571394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173819485-A-G

58571844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173819937-C-T

58571897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173819990-A-G

58571972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173820058-T-C

58571983-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173820069-C-G

58572328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173820392-G-A

58572456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173820524-T-C

58572460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173820528-C-T

58572509-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173820578-C-G

58572519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173820588-A-G

58572522-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173820591-G-C

58574080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173824274-G-A

58574080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173824274-G-T

58574149-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173824341-A-T

58574459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173824616-C-T

58575513-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173828961-A-T

58575666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173829120-C-T

58575820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173829237-G-A

58575820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173829237-G-T

58575865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173829265-G-A

58576016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173829418-G-A

58576127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173829526-T-C

58576311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173829708-T-C

58576326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173829723-G-A

58576349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173829747-G-T

58576363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173829760-T-C

58577902-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173831315-A-T

58578675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173832228-G-A

58578686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173832244-G-A

58578760-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173832326-G-C

58579181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173832703-G-A

58579349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173832850-G-T

58579358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173832869-T-C

58579425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173832920-A-G

58579523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173832998-A-G

http://identifiers.org/hco/20/GRCh38#58579613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173833065-C-A

58580279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173833626-A-G

58583672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173836246-C-T

58583673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173836247-G-A

58583842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173836361-C-T

58584075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173836552-T-C

58584084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173836560-C-T

58584255-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173836695-C-G

58585167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173838046-A-G

58585461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173838354-G-A

58585545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173838429-A-G

58585586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173838470-C-T

58586081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173838921-G-A

58586667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173838961-G-A

58586667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173838961-G-T

58586849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173839112-C-T

58586873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173839135-G-A

58587025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173839244-A-G

58587271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173839409-C-T

58587394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173839506-A-G

58587446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173839556-G-A

58587473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173839582-C-T

58588736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173843887-A-G

58588738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173843889-T-C

58588913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173844032-T-C

58588971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173844085-C-T

58588979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173844093-C-T

58589490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173844754-C-T

http://identifiers.org/hco/20/GRCh38#58592508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173846216-C-A

58592629-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173846325-C-G

58593074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173846787-C-T

58593628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173847216-A-G

58593679-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173847260-G-C

58593698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173847279-G-A

58593712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173847293-A-G

58593738-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173847320-G-C

58594117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173847805-C-T

58594262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173847948-C-T

58594424-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173848105-A-T

58594470-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173848147-G-T

58594517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173848190-G-A

58594517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173848190-G-T

58594537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173848198-T-C

http://identifiers.org/hco/20/GRCh38#58594559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173848216-C-A

58594569-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173848226-G-C

58594569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173848226-G-T

58594588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173848233-G-A

58595028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173848381-A-G

58595225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173848565-C-T

http://identifiers.org/hco/20/GRCh38#58595386-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173848708-A-C

58595386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173848708-A-G

58595476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173848799-A-G

58596148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173849382-T-C

58596283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173849479-A-G

58596289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173849485-G-A

http://identifiers.org/hco/20/GRCh38#58596383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173849554-C-A

58596515-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173849688-C-G

58596982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173850106-C-T

58597201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173850328-G-A

58597226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173850352-G-A

58597300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173850423-G-A

58597300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173850423-G-T

58597624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173850657-C-T

58597779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173850810-C-T

58598027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173851030-C-T

58598028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173851031-G-A

58600042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173851817-C-T

58600043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173851818-G-A

58600168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173851933-G-A

58600610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173852925-A-G

58600696-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173853037-T-A

58601069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173853469-T-C

58601113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173853502-C-T

58601130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173853519-C-T

58602205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173854661-T-C

58603055-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173855760-A-T

58604229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173856800-G-A

58604312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173856861-C-T

58604553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173857186-G-A

58604755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173857383-C-T

58604848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173857502-C-T

58604919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173857569-C-T

58604993-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173857643-A-T

58605101-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173857748-T-A

58605101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173857748-T-C

58605141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173857775-G-A

58605452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173858076-C-T

58607008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173859262-T-C

58607463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173859663-C-T

58607677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173859847-C-T

http://identifiers.org/hco/20/GRCh38#58607755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173859915-C-A

58607755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173859915-C-T

58608710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173860177-C-T

58609084-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173860486-T-A

58609160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173860526-C-T

58609224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173860560-C-T

58609232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173860568-T-C

58609628-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173860928-T-G

58609647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173860946-T-C

58609693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173860985-C-T

58609724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173861017-A-G

58609816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173861102-G-A

58609824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173861110-G-A

58618003-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173861822-C-G

58618014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173861833-G-A

58618084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173861904-G-A

58618250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173862078-T-C

58618359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173862166-C-T

58618597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173862450-G-T

58618947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: non coding transcript exon variant
orthologous variants: 173862776-G-A

58618947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: non coding transcript exon variant
orthologous variants: 173862776-G-T

58618976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: non coding transcript exon variant
orthologous variants: 173862804-G-A

58618976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: non coding transcript exon variant
orthologous variants: 173862804-G-T

http://identifiers.org/hco/20/GRCh38#58619029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173862870-C-A

58619065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: non coding transcript exon variant
orthologous variants: 173862906-T-C

http://identifiers.org/hco/20/GRCh38#58619096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173862939-C-A

58619097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: non coding transcript exon variant
orthologous variants: 173862940-C-T

58619117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: non coding transcript exon variant
orthologous variants: 173862958-T-C

58619130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: non coding transcript exon variant
orthologous variants: 173862970-T-C

58619143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: non coding transcript exon variant
orthologous variants: 173862983-G-T

58619278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: non coding transcript exon variant
orthologous variants: 173863105-G-A

58619278-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: non coding transcript exon variant
orthologous variants: 173863105-G-C

58619278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: non coding transcript exon variant
orthologous variants: 173863105-G-T

58619394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 173863191-G-A

58619394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 173863191-G-T

http://identifiers.org/hco/20/GRCh38#58619465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173863333-C-A

http://identifiers.org/hco/20/GRCh38#58619519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173863401-C-A

58619519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: non coding transcript exon variant
orthologous variants: 173863401-C-T

58619526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: non coding transcript exon variant
orthologous variants: 173863408-G-A

58619563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: non coding transcript exon variant
orthologous variants: 173863487-G-A

58619628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: non coding transcript exon variant
orthologous variants: 173863546-G-A

58619628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: non coding transcript exon variant
orthologous variants: 173863546-G-T

58619651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: non coding transcript exon variant
orthologous variants: 173863570-A-G

http://identifiers.org/hco/20/GRCh38#58619668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#173863585-C-A

58619668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: non coding transcript exon variant
orthologous variants: 173863585-C-T

58619840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27152
most severe consequence: non coding transcript exon variant
orthologous variants: 173863754-G-T