58415458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103296771-T-C

http://identifiers.org/hco/1/GRCh38#58415877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103296410-C-A

58415993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103296290-C-T

58416020-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103296261-T-G

58417072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103295107-C-T

58417241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103294931-T-C

58417311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103294877-A-G

58417319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103294870-G-A

58417323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103294866-G-A

58417323-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103294866-G-C

58418140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103294301-T-C

58418232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103294211-C-T

58418624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103293866-G-A

58419132-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103293065-C-G

58419169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103293100-G-A

58420126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103293694-A-G

58420155-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103293679-T-A

58420155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103293679-T-C

58420248-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103293605-C-G

58421061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103292828-C-T

58421561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103292324-G-A

58421675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103292217-A-G

58421749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103292142-G-T

58421961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103291957-A-G

58421992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103291926-A-G

58422125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103291820-G-A

58422139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103291808-G-A

58422199-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103291751-A-T

58422281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103291678-T-C

58422281-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103291678-T-G

58422282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103291677-A-G

58422432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103291525-G-A

58422876-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103291010-G-C

58423120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103290872-A-G

58423171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103290808-T-C

58423171-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103290808-T-G

58423318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103290661-A-G

58423351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103290628-T-C

58423639-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103290356-G-C

58423640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103290355-G-A

58423812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103290173-C-T

http://identifiers.org/hco/1/GRCh38#58423931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103290056-C-A

58424110-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103289867-C-G

58425696-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103287668-G-C

58426123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103287258-G-A

http://identifiers.org/hco/1/GRCh38#58426453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103286941-C-A

58426707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103286852-T-C

58426757-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103286820-A-T

58426929-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103286663-G-C

58427832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103285152-T-C

58427848-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103285136-T-A

58427857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103285127-G-A

58427997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103284993-G-A

58428152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103284788-G-A

58428299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103284658-C-T

http://identifiers.org/hco/1/GRCh38#58428936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103283937-C-A

58429004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103283871-C-T

58429045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103283833-T-C

58429307-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103283744-G-C

58429308-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103283743-T-G

58429705-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103283475-T-A

58429705-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103283475-T-G

58429761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103283420-C-T

58429801-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103283382-A-T

58430510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103280932-G-A

58430518-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103280924-T-G

58430945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103280461-C-T

58431317-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103280134-T-A

58431472-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103280038-C-G

58431472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103280038-C-T

58431545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103280003-G-A

58431545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103280003-G-T

58431560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103279988-A-G

58431722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103279842-C-T

58431988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103279535-T-C

58432024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103279506-A-G

58432157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103279409-T-C

58432243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103279345-C-T

58432262-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103279327-T-G

58432342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103279228-T-C

58432398-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103279182-G-C

http://identifiers.org/hco/1/GRCh38#58432406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103279174-C-A

58432407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103279173-C-T

58432409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103279171-C-T

58432430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103279164-C-T

58432438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103279156-T-C

58432532-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103279057-T-A

58432620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103278973-A-G

58432880-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103278773-C-G

58432880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103278773-C-T

58433041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103278658-G-A

58435676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103278332-G-A

58435676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103278332-G-T

http://identifiers.org/hco/1/GRCh38#58435677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103278331-C-A

58435677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103278331-C-T

58435725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103278293-G-A

58435865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103278162-G-A

58436002-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103278036-A-T

58436063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103277976-C-T

58436076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103277969-A-G

58436232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103277817-G-T

58436247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103277802-A-G

58436281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103277771-C-T

58436297-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103277755-T-G

http://identifiers.org/hco/1/GRCh38#58436332-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103277715-A-C

58436397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103277647-G-A

58436490-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103277570-T-A

58441190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103268331-G-A

58441350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103268174-A-G

58441634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103267911-T-C

58441941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103267617-G-A

58442105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103267452-C-T

58442218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103267396-G-A

58442238-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103267376-A-T

58442304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103267312-T-C

58442425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103267215-T-C

58442607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103267030-G-A

58443225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103266180-A-G

58443292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103266131-A-G

58443541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103265922-T-C

58443687-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103265713-A-T

58444191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103264679-A-G

58444224-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103264647-T-A

58444344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103264550-A-G

58444956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103263818-G-T

58445032-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103263755-T-A

http://identifiers.org/hco/1/GRCh38#58445371-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103263477-A-C

58445398-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103263454-C-G

http://identifiers.org/hco/1/GRCh38#58446250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103263357-C-A

58446282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103263325-T-C

58446881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103262737-C-T

58447163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103262503-T-C

58447270-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103262393-A-T

58447441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103262222-T-C

58447467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103262191-T-C

http://identifiers.org/hco/1/GRCh38#58448377-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103261223-A-C

58448423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103261146-G-T

58448524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103261047-G-A

58448564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103261010-G-A

58448564-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103261010-G-C

58448613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103260962-G-A

58448649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103260926-A-G

58448761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103260805-G-A

http://identifiers.org/hco/1/GRCh38#58448786-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103260777-A-C

58448789-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103260774-G-C

58448885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103260689-G-A

58449313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103259839-C-T

58454484-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103257943-C-G

58454484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103257943-C-T

58454496-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103257932-C-G

58454521-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103257907-T-G

58454826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103257662-C-T

58455098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103257382-G-A

58455177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103257312-A-G

http://identifiers.org/hco/1/GRCh38#58455258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103257238-C-A

58455365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103257135-G-A

58455378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103257121-C-T

58455599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103256912-T-C

58455623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103256891-A-G

58455631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103256877-G-A

58456343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103254917-T-C

http://identifiers.org/hco/1/GRCh38#58456644-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103254624-A-C

58457151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103253361-G-A

58457370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103253172-G-A

58457419-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103253110-T-G

58457949-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103252589-T-A

58458119-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103252413-T-G

58458750-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103251855-A-T

58458798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103251827-G-A

http://identifiers.org/hco/1/GRCh38#58459069-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103251744-A-C

58459395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103251435-T-C

58460699-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103250088-C-G

http://identifiers.org/hco/1/GRCh38#58460884-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103249746-A-C

58460895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103249736-C-T

58461021-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103249451-G-C

http://identifiers.org/hco/1/GRCh38#58462079-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103248472-C-A

58462079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103248472-C-T

58462518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103248346-G-T

58462530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103248334-T-C

http://identifiers.org/hco/1/GRCh38#58462561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103248303-C-A

58462756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103247438-A-G

http://identifiers.org/hco/1/GRCh38#58462759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103247435-C-A

58462801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 103247393-A-G

58462943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103247275-C-T

58463380-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103246839-A-T

58463623-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103246612-T-A

58463726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103246499-C-T

58463821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103246419-C-T

58463991-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103246277-T-A

58464377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103245910-A-G

58464560-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103245335-T-G

58464955-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103244979-T-G

58464983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103244952-C-T

http://identifiers.org/hco/1/GRCh38#58465172-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103244770-C-A

58465172-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103244770-C-G

58465569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103244433-T-C

58465591-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103244411-T-A

58466828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103239325-T-C

58467039-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103239153-T-A

58467113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103239101-C-T

58467602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103238637-C-T

58467772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103238469-G-A

http://identifiers.org/hco/1/GRCh38#58468512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103238102-C-A

58468610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103238012-A-G

58468644-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103237985-T-A

58468644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103237985-T-C

58468644-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103237985-T-G

58468653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103237976-A-G

58468663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103237966-A-G

http://identifiers.org/hco/1/GRCh38#58468743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103237886-C-A

58468743-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103237886-C-G

58468743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103237886-C-T

58468772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103237856-G-A

58468772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103237856-G-T

58468842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103237784-G-A

58468842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103237784-G-T

58468869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103237761-A-G

58468874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103237756-T-C

http://identifiers.org/hco/1/GRCh38#58468947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103237690-C-A

http://identifiers.org/hco/1/GRCh38#58469105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103237531-C-A

58469154-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103237490-T-G

http://identifiers.org/hco/1/GRCh38#58469160-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103237484-C-A

58469316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103237404-G-A

58469635-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103230753-A-T

58469819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103230568-A-G

58469826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103230561-G-T

58469892-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103230478-A-T

58470707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103229670-C-T

58470968-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103229393-T-A

58471069-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103229287-G-C

58471199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103229181-A-G

http://identifiers.org/hco/1/GRCh38#58471312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103229095-C-A

58471312-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103229095-C-G

58471395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103229021-A-G

58471439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103228980-C-T

58472552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103227904-G-T

58476287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103227450-C-T

58476308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103227429-T-C

58476683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103227243-G-T

58476721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103227205-G-A

58476871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103227058-A-G

http://identifiers.org/hco/1/GRCh38#58476958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103226973-C-A

58476958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103226973-C-T

58477400-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103226540-G-C

58477493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103226441-C-T

58477494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103226440-A-G

58477502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103226432-C-T

58477566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103226364-G-T

58477733-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103226216-G-C

58477850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103226125-T-C

58478399-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103225762-T-A

58479309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103224916-T-C

58479338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103224888-A-G

58479457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103224795-G-T

58479786-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103224575-C-G

58479790-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103224571-G-C

58480087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103224088-T-C

58480151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103224023-C-T

58480543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103223749-C-T

58480710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103223638-A-G

http://identifiers.org/hco/1/GRCh38#58480711-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103223637-A-C

http://identifiers.org/hco/1/GRCh38#58480729-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103223619-A-C

58480780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103223568-A-G

58480904-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103223442-T-A

58480904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103223442-T-C

58480921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103223424-G-T

58480931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103223414-T-C

http://identifiers.org/hco/1/GRCh38#58480937-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103223408-A-C

58480937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103223408-A-G

58480948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103223397-G-A

58480948-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103223397-G-C

58480948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103223397-G-T

58480960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103223385-T-C

58480984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103223361-T-C

58480990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103223355-A-G

58480993-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103223352-T-A

58481074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103223268-T-C

http://identifiers.org/hco/1/GRCh38#58481104-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103223238-A-C

58481112-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 103223230-T-A

58481112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 103223230-T-C

58481115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 103223227-T-C

http://identifiers.org/hco/1/GRCh38#58481163-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103223179-A-C

58481163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 103223179-A-G

58481178-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 103223164-T-A

58481178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 103223164-T-C

58481217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103223150-T-C

58481243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103223144-T-C

58481250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103223137-T-C

58481250-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103223137-T-G

58481259-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103223128-T-A

58481259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103223128-T-C

58481490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103222926-C-T

58481616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103222770-T-C

58485553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103220416-A-G

58485653-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103220344-T-G

58486155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103219890-T-C

58487144-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103218631-G-C

58498928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103216590-T-C

58499712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103216039-C-T

http://identifiers.org/hco/1/GRCh38#58499776-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103215982-A-C

58499992-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103215782-C-G

58499994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103215780-G-A

58500159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103215619-C-T

58500748-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103215108-C-G

http://identifiers.org/hco/1/GRCh38#58501266-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103214607-A-C

58501448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103214267-A-G

58502071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103213592-G-A

58502071-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103213592-G-C

58502507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103213228-C-T

58502790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103212943-C-T

58502876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103212857-A-G

58503070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103212658-A-G

58503423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103212378-C-T

58503571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103212239-G-A

58505969-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103210899-G-C

58506112-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103210794-G-C

58506533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103210391-T-C

58506599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103210268-T-C

58506675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103210194-T-C

58506675-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103210194-T-G

58506797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103210092-G-A

58507031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103209925-C-T

58507130-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103209837-T-G

58507381-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103209612-T-A

http://identifiers.org/hco/1/GRCh38#58513561-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103206217-A-C

58513623-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103206169-C-G

58513919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103205954-A-G

58513946-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103205930-C-G

http://identifiers.org/hco/1/GRCh38#58514061-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103205836-A-C

58514311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103205589-T-C

58514498-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103205465-T-A

58514513-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103205451-C-G

58514568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103205402-A-G

58514738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103205243-A-G

58514809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103205192-G-A

58514821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103205183-T-C

58514925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103205081-T-C

58515238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103204698-A-G

58515378-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103204559-T-A

58515543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103204403-C-T

58515703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103204243-C-T

58515763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103204186-G-T

58516037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103203469-A-G

58516404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103203101-G-T

58516716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103202829-T-C

58517040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103202476-A-G

58517152-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103202365-G-C

58517377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103202144-T-C

58525615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103192639-A-G

58525710-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103192574-T-G

58525730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103192554-G-A

http://identifiers.org/hco/1/GRCh38#58525784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103192503-C-A

58526106-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103192111-T-A

http://identifiers.org/hco/1/GRCh38#58526216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103192014-C-A

58526508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103191745-G-A

58526598-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103191659-T-A

58526598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103191659-T-C

http://identifiers.org/hco/1/GRCh38#58526630-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103191643-C-A

http://identifiers.org/hco/1/GRCh38#58526681-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103191602-A-C

58526739-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103191546-G-C

58526739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103191546-G-T

58526761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103191524-C-T

58526897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103191417-A-G

58526945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103191367-A-G

http://identifiers.org/hco/1/GRCh38#58526978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103191334-C-A

58527157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103188678-T-C

58527206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103188625-T-C

58527580-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103188279-T-A

58527897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103187977-T-C

58527920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103187954-T-C

58528011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103187863-T-C

58528030-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103187844-T-A

58528030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103187844-T-C

http://identifiers.org/hco/1/GRCh38#58528131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103187745-C-A

58528213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103187665-G-A

58528231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103187653-A-G

58528318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103187593-T-C

http://identifiers.org/hco/1/GRCh38#58528463-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103187442-A-C

58528587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103186935-G-A

58528758-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103186774-T-G

58528975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103186545-C-T

58530407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103186320-G-A

58530435-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103186296-A-T

58530458-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103186273-A-T

58530469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103186262-T-C

58530503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103186224-T-C

58530503-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103186224-T-G

http://identifiers.org/hco/1/GRCh38#58530538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103186205-C-A

58530538-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103186205-C-G

58530540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103186203-G-T

58530650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103186112-C-T

58530752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103186010-A-G

58530776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103185986-A-G

http://identifiers.org/hco/1/GRCh38#58530800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103185955-C-A

http://identifiers.org/hco/1/GRCh38#58530812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103185943-C-A

58530812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103185943-C-T

58530838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103185907-A-G

http://identifiers.org/hco/1/GRCh38#58530839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103185906-C-A

http://identifiers.org/hco/1/GRCh38#58530913-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103185663-A-C

58530913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103185663-A-G

58530960-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103185602-A-T

58530961-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103185601-G-T

58530993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103185564-T-C

http://identifiers.org/hco/1/GRCh38#58531335-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103185180-A-C

58531340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103185175-G-A

58531392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103185125-T-C

58532346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103184404-A-G

58532944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103183452-T-C

58532979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103183413-A-G

58532981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103183411-T-C

58533054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103183333-G-A

58533182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103183235-C-T

58533832-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103182715-T-A

58533954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 103182594-G-A

http://identifiers.org/hco/1/GRCh38#58534230-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103182315-A-C

58534235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103182310-C-T

58534312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103182233-T-C

58534340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103182200-T-C

58534400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103182142-G-T

58534518-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103182029-C-G

58534788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103181626-T-C

58534807-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103181462-G-C

58534816-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103181453-T-A

58534816-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103181453-T-G

58534866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103181413-G-A

58534960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103181321-G-A

58535256-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103180954-T-A

58535256-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103180954-T-G

58536057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103179443-T-C

58536105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103179419-A-G

58536107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103179417-T-C

58536139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103179388-C-T

58536163-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103179365-C-G

58536285-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103179273-T-A

http://identifiers.org/hco/1/GRCh38#58536774-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103178804-A-C

http://identifiers.org/hco/1/GRCh38#58536781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103178796-C-A

58536860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103178758-G-A

58536860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103178758-G-T

58536863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103178755-G-A

58536863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103178755-G-T

58536972-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103178658-T-G

58537015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103178614-T-C

58537229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103178482-C-T

58537233-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103178478-G-C

58537283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103178437-C-T

58537362-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103178393-G-C

58537429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103178325-T-C

58537442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103178312-G-A

58537681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103178097-T-C

58537718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103178031-G-A

58537955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103177495-G-A

58537955-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103177495-G-C

58537958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103177492-G-A

58538337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103177148-G-A

58538337-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103177148-G-C

58538663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103176865-G-A

58538663-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103176865-G-C

58538777-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103176742-T-G

58538905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 103176613-T-C

58538936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 103176582-G-A

http://identifiers.org/hco/1/GRCh38#58538985-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103176536-A-C

58538985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 103176536-A-G

58538995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 103176526-C-T

58539058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 103176463-T-C

58539067-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 103176454-G-C

58539067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 103176454-G-T

58539233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 103176297-G-A

58542483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 103174556-T-C

58542661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103174415-A-G

58542886-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103174234-T-A

58542956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103174170-T-C

58543258-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103173868-T-A

58543377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103173768-A-G

58543456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103173695-T-C

58543607-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103173546-T-A

58543607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103173546-T-C

58543681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103173373-G-T

58543683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103173371-C-T

58543809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103173213-C-T

58544400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103172672-G-A

58545215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103172336-A-G

58545390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103172168-A-G

http://identifiers.org/hco/1/GRCh38#58545830-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103171728-A-C

58545967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103171579-T-C

58546345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103171256-G-A

58546515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103171176-T-C

http://identifiers.org/hco/1/GRCh38#58546708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#103171060-C-A

http://identifiers.org/hco/1/GRCh38#58546775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#103170979-C-A

58546775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103170979-C-T

http://identifiers.org/hco/1/GRCh38#58546785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#103170970-C-A

58546785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103170970-C-T

58546786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103170969-G-A

58546786-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103170969-G-C

58546786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29661
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103170969-G-T