58608716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14138203-T-C

58608738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14138181-A-G

58608738-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14138181-A-T

58608744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14138175-G-T

58608759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14138160-G-T

58608781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14138138-G-A

58608781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14138138-G-T

58608796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14138123-G-A

58608796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14138123-G-T

58608813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14138106-G-A

58608813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14138106-G-T

http://identifiers.org/hco/3/GRCh38#58609058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#14137863-C-A

58609058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14137863-C-T

58609067-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14137854-G-C

58609144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14137794-T-C

58609178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14137768-T-C

58609201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14137756-T-C

58609229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14137728-G-A

58609325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14137629-A-G

58609576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14137217-A-G

http://identifiers.org/hco/3/GRCh38#58609668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#14137140-C-A

58609939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14136917-T-C

58610004-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14136873-A-T

58610199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14136707-G-A

58610300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14136649-C-T

58610322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14136616-G-T

58610335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14136604-C-T

58610341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14136598-C-T

58610379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14136559-C-T

58610380-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14136558-G-C

58610566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14136369-G-A

58610593-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14136344-G-C

58617242-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14134044-T-G

58617396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14133888-C-T

58617525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14133764-G-A

58617525-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14133764-G-C

58617525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14133764-G-T

58617757-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14133547-T-A

58617762-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14133541-G-C

58617799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14133514-G-T

58617929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14133434-G-A

58618002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14133372-G-A

58618061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14133320-G-A

58618063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14133319-G-A

58618063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14133319-G-T

58620051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14131520-G-T

58620195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14131371-G-T

58620406-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14131240-C-G

58620667-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14130908-C-G

58620667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14130908-C-T

58620700-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14130876-G-C

58620776-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14130794-C-G

58620776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14130794-C-T

58621024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14130592-G-T

58621056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14130559-G-A

58621174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14130442-G-A

58621354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14130298-G-T

http://identifiers.org/hco/3/GRCh38#58621438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#14130218-C-A

http://identifiers.org/hco/3/GRCh38#58621439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#14130217-C-A

58624129-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14128427-T-A

http://identifiers.org/hco/3/GRCh38#58624179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#14128392-C-A

58624247-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14128322-G-C

58624251-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14128318-G-C

58624273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14128296-A-G

58624284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14128276-A-G

58624290-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14128270-C-G

58624298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14128262-G-A

58624456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14128131-G-A

58624522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14128070-A-G

58624563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14128029-C-T

58626379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14127936-T-C

58626632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14127683-C-T

58626789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14127599-C-T

58626791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14127597-G-A

58626791-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14127597-G-C

http://identifiers.org/hco/3/GRCh38#58626811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#14127577-C-A

58626854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14127538-G-A

58626854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14127538-G-T

http://identifiers.org/hco/3/GRCh38#58626865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#14127527-C-A

58626865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14127527-C-T

58626891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14127503-G-A

58626900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14127494-G-A

58626900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14127494-G-T

58626905-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14127489-C-G

58626905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14127489-C-T

58626921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14127474-G-T

http://identifiers.org/hco/3/GRCh38#58626930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#14127466-C-A

http://identifiers.org/hco/3/GRCh38#58626943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#14127453-C-A

58626943-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14127453-C-G

58626943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14127453-C-T

http://identifiers.org/hco/3/GRCh38#58626990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#14127409-C-A

58626990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 14127409-C-T

58627020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 14127379-G-A

58627024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 14127375-G-A

58627024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 14127375-G-T

http://identifiers.org/hco/3/GRCh38#58627058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#14127342-C-A

58627058-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 14127342-C-G

58627058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 14127342-C-T

58627060-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 14127340-T-A

58627117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 14127328-G-A

58627117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 14127328-G-T

http://identifiers.org/hco/3/GRCh38#58627131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#14127314-C-A

58627131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 14127314-C-T

58627222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 14127242-C-T

58627311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 14127152-G-A

58627311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 14127152-G-T

58627320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 14127139-G-T

58627356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 14127117-T-C

58627356-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 14127117-T-G

58627357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 14127116-A-G

58627373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 14127100-G-A

58627373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 14127100-G-T

http://identifiers.org/hco/3/GRCh38#58627436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#14127064-C-A

58627436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 14127064-C-T

58627450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 14127053-G-A

58627450-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 14127053-G-T

58627463-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 14127040-G-C

58627464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 14127039-G-A

58627464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 14127039-G-T

58627468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 14127035-G-A

58627488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 14127021-G-A

58627488-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 14127021-G-C

58627503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 14127006-A-G

58627506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 14127003-T-C

58627545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 14126963-G-T

58627647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14126869-G-A

58627647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14126869-G-T

http://identifiers.org/hco/3/GRCh38#58627715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#14126802-C-A

58627715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14126802-C-T

58628266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14126072-G-A

58628564-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14125801-T-G

58628693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14125668-G-A

58628700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14125661-C-T

58628857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14125524-C-T

58629306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14123814-G-A

http://identifiers.org/hco/3/GRCh38#58629596-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#14123614-A-C

58629779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14123457-C-T

58629960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14123308-T-C

58629991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14123277-C-T

http://identifiers.org/hco/3/GRCh38#58630013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#14123255-C-A

58630108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14123174-C-T

58630314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 14122986-G-A

58630457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14122851-G-A

58630514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14122794-T-C

58630636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14122699-C-T

58630891-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14122461-G-C

58630897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14122455-C-T

58632222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14122155-G-A

58632222-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14122155-G-C

58632433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14121998-A-G

58632491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14121952-G-T

58632598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14121909-A-G

58633411-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14121253-G-C

http://identifiers.org/hco/3/GRCh38#58633862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#14120914-C-A

58633877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14120900-G-A

58633877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14120900-G-T

58633911-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14120862-G-C

58633911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14120862-G-T

58633927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14120846-G-T

http://identifiers.org/hco/3/GRCh38#58633948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#14120828-C-A

58634011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 14120763-C-T

58634072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 14120709-G-A

58634072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 14120709-G-T

58634073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 14120708-G-T

58634083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 14120698-G-T

58634109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 14120667-G-A

58634109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 14120667-G-T

58634136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 14120640-G-A

58634136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 14120640-G-T

58634156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 14120620-A-G

http://identifiers.org/hco/3/GRCh38#58634193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#14120583-C-A

58634193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 14120583-C-T

58634212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 14120544-G-A

58634212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 14120544-G-T

58634231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 14120526-A-G

58634292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 14120481-G-A

58634401-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14120375-G-C

58634401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14120375-G-T

58634405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14120371-G-T

58634413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14120359-G-A

58634413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14120359-G-T

58634475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14120297-T-C

http://identifiers.org/hco/3/GRCh38#58634530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#14120244-C-A

58634530-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14120244-C-G

58634530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14120244-C-T

58634674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14120109-A-G

58634692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14120093-A-G

58636086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14117913-T-C

58636126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14117882-T-C

http://identifiers.org/hco/3/GRCh38#58636287-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#14117696-A-C

58636398-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 14117585-G-C

58636399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 14117584-T-C

http://identifiers.org/hco/3/GRCh38#58636431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#14117552-C-A

58636431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14117552-C-T

58636484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14117501-G-T

58636500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14117488-G-T

58636857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14116185-A-G

http://identifiers.org/hco/3/GRCh38#58637025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#14116035-C-A

58637025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14116035-C-T

58637073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14115989-G-A

58637073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14115989-G-T

58637164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 14115899-G-A

58637253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 14115811-G-T

58637275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 14115789-G-T

58637318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 14115745-C-T

http://identifiers.org/hco/3/GRCh38#58637332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#14115731-C-A

58637332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 14115731-C-T

58640016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 14114376-T-C

58640019-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 14114373-A-T

58640116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 14114318-G-A

58640119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 14114315-G-A

58640164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 14114270-A-G

58640164-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 14114270-A-T

58640170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 14114264-C-T

58640185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 14114253-T-C

58640219-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 14114219-T-A

58640219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 14114219-T-C

58640274-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 14114164-A-T

http://identifiers.org/hco/3/GRCh38#58640275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#14114163-C-A

58640348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 14114084-G-T

58640456-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 14113983-C-G

58640491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 14113948-A-G

58640585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 14113865-C-T

58640593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 14113857-T-C

58640698-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 14113760-C-G

58640708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 14113750-G-A

58640708-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 14113750-G-C

58641002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 14113508-C-T

58641029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 14113481-T-C

58642943-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 14113137-C-G

58643589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 14112701-A-G

http://identifiers.org/hco/3/GRCh38#58643608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#14112682-C-A

58643608-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 14112682-C-G

58643608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 14112682-C-T

58643696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 14112627-A-G

58643708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant, undefined
orthologous variants: 14112615-A-G

58643720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: 14112603-C-T

58643978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 14112350-T-C

58644112-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 14112235-C-G