41961004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 3 prime UTR variant
orthologous variants: 15904539-T-C

41961107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 3 prime UTR variant
orthologous variants: 15904444-G-A

41961232-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 3 prime UTR variant
orthologous variants: 15904319-A-T

http://identifiers.org/hco/7/GRCh38#41961333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15904220-C-A

41961333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 3 prime UTR variant
orthologous variants: 15904220-C-T

41961715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 3 prime UTR variant
orthologous variants: 15903819-G-A

41961763-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 3 prime UTR variant
orthologous variants: 15903778-T-A

41961763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 3 prime UTR variant
orthologous variants: 15903778-T-C

41961776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 3 prime UTR variant
orthologous variants: 15903765-C-T

41962081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 3 prime UTR variant
orthologous variants: 15903475-C-T

http://identifiers.org/hco/7/GRCh38#41962098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15903460-C-A

41962127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 3 prime UTR variant
orthologous variants: 15903433-G-A

41962127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 3 prime UTR variant
orthologous variants: 15903433-G-T

41962709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 3 prime UTR variant
orthologous variants: 15902879-A-G

41962976-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 3 prime UTR variant
orthologous variants: 15902652-T-A

41962976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 3 prime UTR variant
orthologous variants: 15902652-T-C

http://identifiers.org/hco/7/GRCh38#41963508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15902161-C-A

http://identifiers.org/hco/7/GRCh38#41963570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15902107-C-A

41963742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 3 prime UTR variant
orthologous variants: 15901935-A-G

41963742-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 3 prime UTR variant
orthologous variants: 15901935-A-T

41963767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 3 prime UTR variant
orthologous variants: 15901907-A-G

41963801-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 3 prime UTR variant
orthologous variants: 15901873-T-A

41963801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 3 prime UTR variant
orthologous variants: 15901873-T-C

41963921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 3 prime UTR variant
orthologous variants: 15901761-G-A

41963921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 3 prime UTR variant
orthologous variants: 15901761-G-T

http://identifiers.org/hco/7/GRCh38#41963935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15901747-C-A

41963935-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 3 prime UTR variant
orthologous variants: 15901747-C-G

41963935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 3 prime UTR variant
orthologous variants: 15901747-C-T

41963952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 3 prime UTR variant
orthologous variants: 15901731-G-T

41963984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 3 prime UTR variant
orthologous variants: 15901699-T-C

41964138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 3 prime UTR variant
orthologous variants: 15901540-T-C

41964227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 3 prime UTR variant
orthologous variants: 15901450-T-C

41964303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 3 prime UTR variant
orthologous variants: 15901391-T-C

41964325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 3 prime UTR variant
orthologous variants: 15901369-A-G

41964370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: missense variant
orthologous variants: 15901324-G-A

41964370-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: missense variant
orthologous variants: 15901324-G-C

41964370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: missense variant
orthologous variants: 15901324-G-T

41964390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: synonymous variant
orthologous variants: 15901304-G-A

41964390-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: missense variant
orthologous variants: 15901304-G-C

41964448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: missense variant
orthologous variants: 15901246-C-T

41964484-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: missense variant
orthologous variants: 15901210-T-A

41964792-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: synonymous variant
orthologous variants: 15900902-C-G

http://identifiers.org/hco/7/GRCh38#41964961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15900733-C-A

41964999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: synonymous variant
orthologous variants: 15900695-T-C

41965024-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: missense variant
orthologous variants: 15900670-G-C

41965081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: missense variant
orthologous variants: 15900613-C-T

41965152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: synonymous variant
orthologous variants: 15900542-G-A

41965198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: missense variant
orthologous variants: 15900496-T-C

41965251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: synonymous variant
orthologous variants: 15900443-G-A

41965251-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: synonymous variant
orthologous variants: 15900443-G-C

41965264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: missense variant
orthologous variants: 15900430-C-T

41965452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: synonymous variant
orthologous variants: 15900242-G-A

41965452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: missense variant
orthologous variants: 15900242-G-T

41965517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: missense variant
orthologous variants: 15900171-G-A

http://identifiers.org/hco/7/GRCh38#41965565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15900120-C-A

41965565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: missense variant
orthologous variants: 15900120-C-T

41965677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: synonymous variant
orthologous variants: 15900008-G-A

41965677-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: synonymous variant
orthologous variants: 15900008-G-C

41965900-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: missense variant
orthologous variants: 15899785-C-G

41965900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: missense variant
orthologous variants: 15899785-C-T

41965957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: missense variant
orthologous variants: 15899728-G-A

41965957-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: missense variant
orthologous variants: 15899728-G-C

41965957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: missense variant
orthologous variants: 15899728-G-T

41965978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: missense variant
orthologous variants: 15899707-G-A

41965978-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: missense variant
orthologous variants: 15899707-G-C

41965978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: missense variant
orthologous variants: 15899707-G-T

41966113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: missense variant
orthologous variants: 15899572-T-C

http://identifiers.org/hco/7/GRCh38#41966173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15899512-C-A

41966428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: missense variant
orthologous variants: 15899257-G-A

41966428-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: missense variant
orthologous variants: 15899257-G-C

41966563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: missense variant
orthologous variants: 15899122-T-C

41966620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: missense variant
orthologous variants: 15899065-C-T

41967447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15898527-G-A

41967453-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15898521-T-A

41967453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15898521-T-C

41967482-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15898494-A-T

41967535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15898411-T-C

41967535-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15898411-T-G

41967613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: missense variant
orthologous variants: 15898333-G-A

41967631-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: missense variant
orthologous variants: 15898315-G-C

41967951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15897995-A-G

http://identifiers.org/hco/7/GRCh38#41968024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15897924-C-A

41968109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15897847-G-A

41968267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15897690-G-A

41968449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15897523-T-C

41968820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15897319-C-T

http://identifiers.org/hco/7/GRCh38#41968940-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15897220-A-C

41968940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15897220-A-G

41968963-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15897201-C-G

41968977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15897186-A-G

41969035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15897144-A-G

41969141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15897041-C-T

41969170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15897029-G-T

41969373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15896873-T-C

http://identifiers.org/hco/7/GRCh38#41969382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15896864-C-A

41969978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15896270-A-G

41970261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15896001-G-A

41970356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15895909-A-G

41970379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15895894-A-G

http://identifiers.org/hco/7/GRCh38#41972207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15895056-C-A

41972249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15895017-G-A

41972298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15894969-G-T

41972374-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: missense variant
orthologous variants: 15894891-C-G

http://identifiers.org/hco/7/GRCh38#41972602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15894663-C-A

41972710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15894568-T-C

41972711-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15894567-T-G

41973234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15894092-G-A

41973311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15894028-A-G

41973425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15893914-A-G

41973521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15893836-C-T

http://identifiers.org/hco/7/GRCh38#41973812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15893189-C-A

41974161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15892844-T-C

41974599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15892185-T-C

41974931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15891909-T-C

41974948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15891892-G-T

41975439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15891539-G-A

41975439-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15891539-G-C

41975961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15891055-A-G

41975979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15891044-T-C

41976016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15891019-G-A

41976108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15890962-C-T

41976155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15890918-T-C

41976232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15890866-G-A

41976312-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15890793-A-T

41976326-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15890772-T-A

41976343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15890759-G-A

http://identifiers.org/hco/7/GRCh38#41976750-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15890415-A-C

41976840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15890330-G-A

41976858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15890312-A-G

41977123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15890082-G-A

41977197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15890006-G-A

41977245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15889954-C-T

41977425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15889797-A-G

41977427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15889795-G-A

41977427-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15889795-G-C

41977432-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15889780-G-C

41977432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15889780-G-T

41977850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 15889405-A-G

41977899-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 15889356-A-T

41977940-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15889315-A-T

41978482-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15888366-A-T

41978542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15888317-G-T

http://identifiers.org/hco/7/GRCh38#41978583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15888271-C-A

41978583-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15888271-C-G

41978583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15888271-C-T

41979298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15887713-G-A

41979298-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15887713-G-C

41979482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15887138-T-C

41979808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15886665-T-C

http://identifiers.org/hco/7/GRCh38#41979820-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15886654-A-C

41980054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15886446-A-G

41980739-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15885837-A-T

41981059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15885305-A-G

41981658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15884735-C-T

41981703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15884694-G-A

41981758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15884667-G-A

41981830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15884615-C-T

41982377-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15884136-C-G

41983086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15883588-A-G

41983148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15883479-T-C

41983249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15883396-C-T

41983330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15883323-G-A

41983444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15883217-G-A

41983696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15882963-G-A

41983779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15882896-T-C

41983847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15882855-G-A

41984194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15882506-G-T

41984426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15882265-T-C

41984426-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15882265-T-G

41984701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15882000-C-T

41984939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15881724-C-T

41984957-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15881706-G-C

41985075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15881635-G-T

41985965-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15881090-G-T

41986122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15880951-T-C

http://identifiers.org/hco/7/GRCh38#41986136-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15880942-A-C

41986158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15880918-T-C

41986180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15880896-G-A

41986180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15880896-G-T

http://identifiers.org/hco/7/GRCh38#41986409-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15880695-A-C

http://identifiers.org/hco/7/GRCh38#41986430-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15880660-A-C

http://identifiers.org/hco/7/GRCh38#41986432-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15880658-A-C

41986647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15880443-T-C

41986704-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15880373-C-G

http://identifiers.org/hco/7/GRCh38#41986848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15880293-C-A

41987039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15880106-T-C

http://identifiers.org/hco/7/GRCh38#41989260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15878611-C-A

http://identifiers.org/hco/7/GRCh38#41989302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15878567-C-A

41989506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15878373-G-T

http://identifiers.org/hco/7/GRCh38#41989565-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15878308-A-C

41989685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15878196-A-G

41990215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15877991-C-T

41990284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15877924-C-T

41990429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15877803-G-A

41990876-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron_variant, undefined
orthologous variants: 15877161-G-C

41991069-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron_variant, undefined
orthologous variants: 15877006-T-G

41991079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron_variant, undefined
orthologous variants: 15876996-A-G

41991111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron_variant, undefined
orthologous variants: 15876965-T-C

41991357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15876765-C-T

41991379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15876744-A-G

41991884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15875612-G-A

41991931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15875565-A-G

41993662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15874750-G-T

41994212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15874246-G-A

41994290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15874180-A-G

41994359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15874111-G-A

41994831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15873638-T-C

41994884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15873573-T-C

41994886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15873571-C-T

41994887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15873570-G-A

http://identifiers.org/hco/7/GRCh38#41995037-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15873450-A-C

41995135-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15873365-T-A

41995277-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15873230-C-G

41995277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15873230-C-T

41996295-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15871511-T-A

41996618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron_variant, undefined
orthologous variants: 15871190-G-A

41997311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15870534-T-C

41997685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15870183-G-A

41997823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15870046-T-C

41997823-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15870046-T-G

41997840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15870029-C-T

http://identifiers.org/hco/7/GRCh38#41998672-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15869543-A-C

41998672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15869543-A-G

http://identifiers.org/hco/7/GRCh38#41998742-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15869462-A-C

41998966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15869259-G-A

42002416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15862143-T-C

42002467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15862094-T-C

42002800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15861743-C-T

42003036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15861555-G-A

42003256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15861339-G-A

42003511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15857410-A-G

42003656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15857279-C-T

http://identifiers.org/hco/7/GRCh38#42004132-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15856817-A-C

42004137-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15856812-T-A

42004836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15856156-G-A

42005302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15854755-G-A

42005355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15854515-A-G

42005366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15854512-C-T

http://identifiers.org/hco/7/GRCh38#42005373-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15854505-A-C

42005542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15853066-C-T

42005556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15853052-C-T

42005627-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15852983-G-C

42005635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15852975-A-G

42006775-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15851217-A-T

http://identifiers.org/hco/7/GRCh38#42006843-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15851153-A-C

42007023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15850893-G-A

42007023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15850893-G-T

42007089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15850836-C-T

http://identifiers.org/hco/7/GRCh38#42007248-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15850660-A-C

42007471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15849746-A-G

42007565-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15849698-G-C

42007763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15849526-C-T

42008781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15849137-C-T

42008802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15849116-A-G

42010902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15847634-A-G

http://identifiers.org/hco/7/GRCh38#42011014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15847533-C-A

http://identifiers.org/hco/7/GRCh38#42011216-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15847331-A-C

http://identifiers.org/hco/7/GRCh38#42011314-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15847237-A-C

42011321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15847230-G-A

42011549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15847039-G-T

http://identifiers.org/hco/7/GRCh38#42011802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15846769-C-A

42012017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15845700-C-T

http://identifiers.org/hco/7/GRCh38#42012381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15845339-C-A

42012381-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15845339-C-G

42012650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15845070-G-A

42012895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15844821-G-A

42013710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15844578-A-G

42013736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15844549-A-G

http://identifiers.org/hco/7/GRCh38#42013820-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15844464-A-C

42013842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15844440-T-C

42013990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15844324-A-G

42014575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15843886-C-T

42014672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15843794-T-C

http://identifiers.org/hco/7/GRCh38#42014696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15843770-C-A

42014874-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15843610-G-C

42014995-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15843487-C-G

42015766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15842768-T-C

42015766-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15842768-T-G

42015856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15842677-G-A

http://identifiers.org/hco/7/GRCh38#42015875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15842651-C-A

42015875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15842651-C-T

42015902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15842635-G-A

42015902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15842635-G-T

42015956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15842592-G-A

http://identifiers.org/hco/7/GRCh38#42016068-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15842502-A-C

http://identifiers.org/hco/7/GRCh38#42016249-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15842370-A-C

42016249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15842370-A-G

42016253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15842368-A-G

42016311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15842325-C-T

42016312-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15842324-T-G

42017821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15841887-G-A

42018053-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15841667-T-A

42018053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15841667-T-C

42018063-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15841656-G-C

http://identifiers.org/hco/7/GRCh38#42018137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15841590-C-A

http://identifiers.org/hco/7/GRCh38#42018190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15841536-C-A

42018190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15841536-C-T

42018398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15841327-C-T

42018786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15840990-C-T

42018938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15840847-A-G

42019160-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15840597-T-A

http://identifiers.org/hco/7/GRCh38#42019342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15840466-C-A

42019342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15840466-C-T

42019584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15840278-G-A

http://identifiers.org/hco/7/GRCh38#42019657-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15840213-A-C

42019796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15840068-G-A

42019993-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15839874-T-A

42020022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15839845-C-T

42020161-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15839704-T-G

42020174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15839691-A-G

42020583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15839278-C-T

42020935-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15839173-T-A

42021191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15838950-T-C

42021213-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15838928-C-G

42021213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15838928-C-T

42021479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15838666-G-A

42022227-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15838182-A-T

42022267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15838144-T-C

42022287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15838123-G-A

42022287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15838123-G-T

42022321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15838083-G-A

42022322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15838082-A-G

42022355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15838050-G-A

42022408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15838008-G-A

42022603-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15837881-T-A

42022604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15837880-G-T

42022667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15837814-C-T

42022734-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15837748-G-C

42022817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15837703-T-C

42023009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15837569-A-G

42023196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15837388-G-A

42023481-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: missense variant
orthologous variants: 15837100-T-G

42023695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15836904-C-T

42023708-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15836891-T-G

42023969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15836788-T-C

42024162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15836614-G-A

42024404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15836357-A-G

42024475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15836282-G-A

42024544-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15836213-A-T

http://identifiers.org/hco/7/GRCh38#42024553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15836204-C-A

42024604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15836156-G-A

42024607-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15836153-T-G

42024664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15836096-G-T

42025057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15835761-T-C

42025203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15835632-G-A

42025203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15835632-G-T

http://identifiers.org/hco/7/GRCh38#42025215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15835620-C-A

42025215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15835620-C-T

42025283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: missense variant
orthologous variants: 15835558-G-A

42025283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: missense variant
orthologous variants: 15835558-G-T

42025396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15835445-G-A

42025396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15835445-G-T

42025445-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15835396-A-T

42025462-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15835385-G-C

42025462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15835385-G-T

42025946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15834969-G-A

42026048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15834887-T-C

42026056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15834881-A-G

42026085-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15834856-A-T

http://identifiers.org/hco/7/GRCh38#42026142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15834802-C-A

42026142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15834802-C-T

42026170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15834773-G-A

42026170-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15834773-G-C

42026170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15834773-G-T

42026248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: missense variant
orthologous variants: 15834709-G-A

42026248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: missense variant
orthologous variants: 15834709-G-T

42026260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: missense variant
orthologous variants: 15834697-G-A

42026260-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: missense variant
orthologous variants: 15834697-G-C

42026317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: missense variant
orthologous variants: 15834640-C-T

42026426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15834532-A-G

42027278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15833675-C-T

http://identifiers.org/hco/7/GRCh38#42028230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15832735-C-A

http://identifiers.org/hco/7/GRCh38#42028276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15832690-C-A

http://identifiers.org/hco/7/GRCh38#42028362-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15832601-A-C

http://identifiers.org/hco/7/GRCh38#42028384-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15832579-A-C

42030248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15832362-C-T

42030264-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15832346-T-A

42030358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15832277-C-T

42030481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15832077-G-A

http://identifiers.org/hco/7/GRCh38#42030592-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15831972-A-C

42030603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15831961-A-G

42032052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15830956-A-G

42032477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15830527-T-C

42032749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15830287-G-T

http://identifiers.org/hco/7/GRCh38#42032911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15830124-C-A

42032911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15830124-C-T

42032928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15830106-G-A

42032928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15830106-G-T

42033269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15829718-C-T

42033805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15829146-T-C

http://identifiers.org/hco/7/GRCh38#42034041-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15828899-A-C

42034198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15828758-T-C

42034201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15828755-A-G

42034535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15828495-G-A

42034562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15828468-C-T

42034663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15828357-G-A

42034721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15828307-C-T

42034722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15828306-C-T

42034730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15828301-C-T

42035270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15827486-G-T

42035457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15827305-A-G

42035480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15827283-T-C

42035493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15827269-G-A

42035493-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15827269-G-C

42035587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15827173-T-C

42035587-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15827173-T-G

42035600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15827162-T-C

http://identifiers.org/hco/7/GRCh38#42036695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15826973-C-A

42036807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15826857-T-C

42038753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15826243-T-C

42038783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15826199-T-C

42039144-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15823971-T-G

42039481-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15823708-T-A

42040059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: missense variant
orthologous variants: 15823284-T-C

42040122-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: missense variant
orthologous variants: 15823221-T-A

42040122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: missense variant
orthologous variants: 15823221-T-C

42040173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: missense variant
orthologous variants: 15823170-G-A

http://identifiers.org/hco/7/GRCh38#42040320-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15823027-A-C

42040597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15822750-G-A

42040685-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15822638-T-A

42040807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15822516-G-A

42041059-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15822315-G-C

42041059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15822315-G-T

42041136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15822236-C-T

42041271-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15822154-G-C

42041410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15822019-C-T

42042609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15821151-A-G

42042777-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15821005-C-G

http://identifiers.org/hco/7/GRCh38#42043507-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15820681-A-C

http://identifiers.org/hco/7/GRCh38#42044017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15820155-C-A

http://identifiers.org/hco/7/GRCh38#42044032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15820141-C-A

42044123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15820052-C-T

42044139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15820032-C-T

42044271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15819910-C-T

http://identifiers.org/hco/7/GRCh38#42044380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15819827-C-A

http://identifiers.org/hco/7/GRCh38#42045305-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15819103-A-C

42045305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15819103-A-G

42045361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15819046-T-C

42045464-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: missense variant
orthologous variants: 15818943-C-G

42045464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: missense variant
orthologous variants: 15818943-C-T

42045584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15818827-T-C

42045763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15818661-G-A

42045984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15818260-C-T

42046037-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15818204-A-T

42046239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15818006-G-A

42046431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15817826-T-C

42047312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15816918-G-T

42047585-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15816656-G-C

42047660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15816581-A-G

42047763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15816520-T-C

42047865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15816429-T-C

42047877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15816417-T-C

42047907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15816384-A-G

http://identifiers.org/hco/7/GRCh38#42047921-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15816367-A-C

42048275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15816042-G-A

http://identifiers.org/hco/7/GRCh38#42048347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15815976-C-A

42048347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15815976-C-T

http://identifiers.org/hco/7/GRCh38#42048364-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15815959-C-A

42048364-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15815959-C-G

42048364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15815959-C-T

42048372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15815947-A-G

42048375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15815944-G-A

42048375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15815944-G-T

42048397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15815922-T-C

http://identifiers.org/hco/7/GRCh38#42048398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15815921-C-A

42048398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15815921-C-T

http://identifiers.org/hco/7/GRCh38#42048405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15815914-C-A

42048619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: missense variant
orthologous variants: 15815729-G-T

42048744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15815607-T-C

42048917-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15815403-T-A

http://identifiers.org/hco/7/GRCh38#42048962-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15815338-A-C

42048962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15815338-A-G

42049438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15814797-T-C

42049535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15814698-G-A

42049812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15814444-C-T

42049839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15814426-G-A

42049839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15814426-G-T

42049943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15814346-A-G

42049943-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15814346-A-T

42050003-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15814278-G-C

http://identifiers.org/hco/7/GRCh38#42050640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15813700-C-A

42050722-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15813618-G-C

http://identifiers.org/hco/7/GRCh38#42050769-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15813571-A-C

42050788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15813546-C-T

http://identifiers.org/hco/7/GRCh38#42050790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15813544-C-A

42051074-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15813279-C-G

42051074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15813279-C-T

42051120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15813237-G-A

42051173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15813186-G-A

42051557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15812758-A-G

42051663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15812643-A-G

42051904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15812374-G-A

42051976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15812294-C-T

42052195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15812054-A-G

http://identifiers.org/hco/7/GRCh38#42052371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15811915-C-A

42052372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15811914-C-T

42052523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15811761-T-C

42052534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15811742-T-C

http://identifiers.org/hco/7/GRCh38#42052646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15811657-C-A

42052646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15811657-C-T

42053349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15810920-C-T

http://identifiers.org/hco/7/GRCh38#42053682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15810598-C-A

http://identifiers.org/hco/7/GRCh38#42053804-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15810495-A-C

42053854-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15810443-C-G

42053879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15810418-G-A

42054048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15810249-C-T

42054054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15810243-C-T

http://identifiers.org/hco/7/GRCh38#42054079-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15810203-C-A

42054282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15809965-A-G

http://identifiers.org/hco/7/GRCh38#42054291-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15809956-A-C

42058445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15809275-C-T

42058569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15809157-A-G

42058726-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15809005-A-T

42058938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15808816-G-A

http://identifiers.org/hco/7/GRCh38#42059003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15808749-C-A

42059221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15808306-T-C

42059221-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15808306-T-G

42060152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15807493-T-C

42060344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15807314-T-C

42060590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15806903-C-T

http://identifiers.org/hco/7/GRCh38#42060679-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15806813-A-C

42062608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15803028-T-C

42062712-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15802923-G-C

http://identifiers.org/hco/7/GRCh38#42062720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15802915-C-A

42063080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15802561-G-A

42063629-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15802064-A-T

42064404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15801658-G-T

42064838-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15801223-G-C

42064988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15801094-G-A

42064988-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15801094-G-C

42065425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15800185-C-T

42066476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15799138-A-G

42066583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15799030-C-T

42066705-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15798919-C-G

42066744-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15798883-C-G

42066825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15798807-C-T

42067676-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15798299-G-C

42067712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15798295-C-T

42068327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15796577-C-T

http://identifiers.org/hco/7/GRCh38#42068521-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15796408-A-C

42068561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15796368-A-G

42068623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15796304-A-G

42069012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15795933-T-C

42069073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15795872-T-C

42069242-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15795701-T-G

42069440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15795506-T-C

42069448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15795498-T-C

http://identifiers.org/hco/7/GRCh38#42069552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15795411-C-A

42069592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15795372-A-G

42069803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15795218-A-G

42069894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15795137-T-C

42070065-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron_variant, undefined
orthologous variants: 15794966-A-T

42070112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron_variant, undefined
orthologous variants: 15794919-G-A

42070283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron_variant, undefined
orthologous variants: 15794819-C-T

42070481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron_variant, undefined
orthologous variants: 15794663-G-A

42070481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron_variant, undefined
orthologous variants: 15794663-G-T

42070705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15794449-A-G

42071225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15793707-G-A

42071225-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15793707-G-C

42071225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15793707-G-T

42071446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15793510-T-C

42071456-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15793500-A-T

http://identifiers.org/hco/7/GRCh38#42071498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15793456-C-A

42071531-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15793437-G-C

42071577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15793390-A-G

42071611-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15793358-G-C

42071650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15793316-A-G

42071676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15793290-A-G

42071880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15793092-G-A

42072019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15792984-T-C

42072086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15792914-C-T

42072430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15792550-G-T

http://identifiers.org/hco/7/GRCh38#42072541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15792380-C-A

42072691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15792240-G-A

http://identifiers.org/hco/7/GRCh38#42072758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15792183-C-A

42072814-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15792128-T-G

42072913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15792044-G-A

42073021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15791954-A-G

42073128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15791854-A-G

42073226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15791757-G-A

http://identifiers.org/hco/7/GRCh38#42073349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15791635-C-A

42073349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15791635-C-T

42073698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15791287-A-G

42073859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15791124-A-G

42073963-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15791043-T-A

42074053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15790959-A-G

42074110-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15790919-C-G

42074110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15790919-C-T

42074341-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15790726-C-G

42074467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15790615-C-T

http://identifiers.org/hco/7/GRCh38#42074479-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15790603-A-C

42074669-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15790517-C-G

42074669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15790517-C-T

42074731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15790461-A-G

42074797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15790397-T-C

42074924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15790272-A-G

42074977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15790221-C-T

42074980-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15790215-C-G

42074983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15790212-A-G

42075071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15790146-A-G

42075599-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15789635-T-G

42075623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15789611-G-A

42076403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15788832-G-A

42076521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15788695-T-C

42076553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15788663-G-A

42076601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15788618-G-A

42076601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15788618-G-T

42076614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15788603-T-C

42076615-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15788602-G-T

42076914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15788305-G-A

42076914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15788305-G-T

http://identifiers.org/hco/7/GRCh38#42077705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15787980-C-A

42078408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15787273-G-A

42078578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15787105-T-C

42079262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15786819-G-A

42079271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15786810-A-G

42079354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15786698-C-T

42079363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15786689-A-G

42079377-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15786675-C-G

http://identifiers.org/hco/7/GRCh38#42079475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15786570-C-A

42079527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15786540-C-T

42079616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15786459-C-T

42079646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15786429-C-T

42080346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15786193-T-C

42080380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15786160-G-A

42080463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15786076-T-C

42080580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15785981-G-A

42080673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15785892-G-T

42081172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15785432-G-A

42081172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15785432-G-T

42081371-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15785233-C-G

42081376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15785228-A-G

42081844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15784760-G-A

42081986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15784630-T-C

42082151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15784506-G-A

42082151-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15784506-G-C

42082333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15784350-T-C

42082333-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15784350-T-G

42082587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15784118-C-T

42082718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15783920-G-T

42083858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15783447-A-G

42084097-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15783199-T-A

42084153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15783140-T-C

42084528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15781616-G-A

42084770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15781377-G-A

42084847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15781297-G-T

42085178-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15781199-C-G

http://identifiers.org/hco/7/GRCh38#42085459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15780987-C-A

42085459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15780987-C-T

http://identifiers.org/hco/7/GRCh38#42085708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15780791-C-A

42086055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15780381-A-G

42086232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15780211-C-T

42087620-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15779275-T-A

42088698-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15778295-T-G

42091411-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15777967-A-T

42091494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15777899-G-A

42091528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15777867-A-G

42091664-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15777752-C-G

42091664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15777752-C-T

42092020-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15777412-C-G

http://identifiers.org/hco/7/GRCh38#42092096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15777326-C-A

42092138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15777283-G-A

42092164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15777257-C-T

42092338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15777007-G-A

42093504-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15775257-G-C

http://identifiers.org/hco/7/GRCh38#42093710-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15775087-A-C

42093710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15775087-A-G

42093759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15775040-C-T

42093794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15775009-C-T

42093797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15775006-T-C

42094255-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15773722-G-C

42095237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15773183-G-A

42095351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15773063-C-T

42095359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15773055-T-C

42095550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15772865-T-C

42095988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15772518-A-G

42096028-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15772479-C-G

42096233-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15772295-T-A

42096316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15772194-C-T

http://identifiers.org/hco/7/GRCh38#42096345-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15772164-A-C

42096372-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15772118-G-C

42096580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15771911-C-T

42096740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15771812-G-A

42097463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15771343-G-A

42097542-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15771285-C-G

42097554-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15771273-C-G

42097830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15771068-C-T

http://identifiers.org/hco/7/GRCh38#42098037-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#15770967-A-C

42099233-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15769436-C-G

42099233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15769436-C-T

42103542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15768216-G-A

42104065-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15767240-T-G

42104139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15767172-G-A

42104165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15767146-A-G

42104165-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15767146-A-T

42104219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15767092-T-C

42104327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15766990-G-A

http://identifiers.org/hco/7/GRCh38#42104421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15766896-C-A

42104421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15766896-C-T

42104755-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15766135-G-C

42105291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15765631-C-T

42105479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15765501-G-T

42105585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15765433-G-A

42105603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15765408-G-A

42105744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15765283-C-T

42105897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15765127-A-G

42106276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15764702-T-C

42106464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15764518-G-A

42106464-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15764518-G-C

42106483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15764502-T-C

42106526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15764458-C-T

42106527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15764457-T-C

42106543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15764441-C-T

42106568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15764412-G-T

42106659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15764321-A-G

42107952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15763315-G-A

42107952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15763315-G-T

42108208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15763083-C-T

42108288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15763049-A-G

42109684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15761149-C-T

42109735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15761098-A-G

42110378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15760595-G-A

42110563-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15760417-G-C

42110563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15760417-G-T

42110749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15759962-G-A

42110811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15759900-G-A

42111060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15759509-T-C

42111172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15759435-C-T

42111253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15759348-G-A

42111396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15759118-G-T

42111436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15759077-G-A

42111436-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15759077-G-C

42111644-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15758885-A-T

42111650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15758879-A-G

42111839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15758689-T-C

http://identifiers.org/hco/7/GRCh38#42116027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15756900-C-A

42116074-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15756875-T-A

42116074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15756875-T-C

42116129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15756822-G-A

http://identifiers.org/hco/7/GRCh38#42116452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15756499-C-A

42116536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15756428-G-A

42116539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15756425-G-A

42116558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15756406-T-C

http://identifiers.org/hco/7/GRCh38#42116643-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15756321-A-C

42116734-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15756244-T-G

42117456-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15755592-T-G

42117653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15755387-C-T

42117865-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15755175-C-G

42117865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15755175-C-T

42119294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15752999-G-A

42119294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15752999-G-T

42119349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15752945-T-C

42119574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15752710-A-G

42119867-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15752394-T-G

42120387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15751863-G-A

42120387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15751863-G-T

http://identifiers.org/hco/7/GRCh38#42120766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15751494-C-A

42121209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15751083-T-C

42121349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15750972-G-A

42121575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15750720-C-T

42121577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15750718-C-T

42121588-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15750704-T-A

42121702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15750608-A-G

42121721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15750591-C-T

42121933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15750294-T-C

42122034-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15750205-T-G

42122236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15750042-T-C

42122335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15749953-A-G

42122524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15749783-C-T

42122659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15749657-T-C

42122890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15749463-C-T

42122953-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15749387-T-A

42123102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15749256-T-C

42123378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15749018-A-G

42123501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15748072-A-G

42123693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15747900-A-G

42123736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15747880-G-A

42123836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15747848-C-T

42123897-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15747835-A-T

42123963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15747782-T-C

42124018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15747733-C-T

42124064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15747691-A-G

42124394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15747397-T-C

42124536-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15746933-G-C

42124571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15746899-C-T

42124830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15746668-T-C

42124907-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15746573-T-G

http://identifiers.org/hco/7/GRCh38#42125116-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15746288-A-C

42125168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15746219-T-C

42125300-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15746090-C-G

42125840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15745561-A-G

42126203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15745203-T-C

42126268-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15745142-C-G

42126376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15745038-T-C

42126403-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15745012-T-A

42126403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15745012-T-C

42126468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15744966-A-G

42126500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15744934-A-G

42126644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15744830-A-G

http://identifiers.org/hco/7/GRCh38#42126858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15744480-C-A

42126858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15744480-C-T

42127554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15744287-T-C

42128604-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15742724-A-T

42129115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15739662-A-G

42129236-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15739564-T-A

42129448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15739384-T-C

42129824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15739327-A-G

http://identifiers.org/hco/7/GRCh38#42129898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15739254-C-A

42129939-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15739214-T-G

42129974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15739179-C-T

42130008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15739146-G-A

42130130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15739026-G-A

42130152-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15739003-C-G

42130172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15738983-A-G

42130182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15738974-G-A

42130182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15738974-G-T

42131827-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15738617-A-T

42131911-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15738532-G-C

42132160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15738299-G-A

42132186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15738269-C-T

42132226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15738235-G-A

42132241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15738220-C-T

42132243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15738218-G-A

42132480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15738094-A-G

42132610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15737951-G-A

42133271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15737203-A-G

42133410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15737067-T-C

42133628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15736876-G-A

42134227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15735889-C-T

42134501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15735637-C-T

42134507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15735631-A-G

42135022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15735012-G-A

42135241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15734819-A-G

42135241-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15734819-A-T

42135455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15734610-C-T

42135478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15734587-T-C

42135661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15734438-C-T

42135963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15734191-C-T

42135973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15734182-G-A

42135999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15734155-T-C

42136018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15734136-A-G

42136028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15734125-G-A

42136206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15733959-C-T

http://identifiers.org/hco/7/GRCh38#42136225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15733937-C-A

42136225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15733937-C-T

42136747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15733247-G-T

42136948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15733051-C-T

42137122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15732910-G-A

42137242-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15732796-C-G

42137242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15732796-C-T

42139251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15730895-C-T

42140067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15730443-G-T

42140472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15729931-C-T

42140476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15729927-A-G

42140499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15729905-A-G

42140765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15729661-T-C

42140997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15729474-G-A

http://identifiers.org/hco/7/GRCh38#42141151-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15729316-A-C

42141335-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15729158-T-A

42142339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15728616-A-G

42142352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15728603-A-G

42142383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15728578-A-G

42143180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15728103-C-T

42143314-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15727976-G-C

42143875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15727380-A-G

42144021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15727235-T-C

42144214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15727041-A-G

42144319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15726929-T-C

42144321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15726927-C-T

http://identifiers.org/hco/7/GRCh38#42144336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15726912-C-A

42144336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15726912-C-T

42144337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15726911-G-A

42144370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15726878-C-T

42144446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15726802-C-T

42144471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15726774-C-T

42144699-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15726531-C-G

42144699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15726531-C-T

42144888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15726362-G-A

42144965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15726286-C-T

42145194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15726075-G-T

42145251-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15726021-T-A

42145333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 15725947-C-T

42145455-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 15725870-T-A

42145455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 15725870-T-C

42145455-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 15725870-T-G

42145521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 15725811-G-A

42145521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 15725811-G-T

42145535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 15725797-A-G

42145604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant, synonymous_variant
orthologous variants: 15725745-G-A

42145604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, splice_region_variant
orthologous variants: 15725745-G-T

http://identifiers.org/hco/7/GRCh38#42145695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15725689-C-A

42145897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15725524-T-C

http://identifiers.org/hco/7/GRCh38#42146168-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15725284-A-C

42146256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15725196-A-G

42146370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15725087-G-A

42147157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15724327-G-A

http://identifiers.org/hco/7/GRCh38#42147564-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15723920-A-C

42147866-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15723606-C-G

http://identifiers.org/hco/7/GRCh38#42147883-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15723589-A-C

42147988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15723485-G-A

42148005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15723466-T-C

http://identifiers.org/hco/7/GRCh38#42148010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15723461-C-A

42148085-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15723390-G-C

42148119-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15723348-A-T

42148135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15723323-G-A

42148135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15723323-G-T

42148136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15723322-C-T

42148151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15723307-A-G

42148156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15723302-C-T

42148170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15723285-C-T

42148199-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15723253-C-G

42148199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15723253-C-T

42148243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 15723208-T-C

42148570-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15722885-A-T

42148572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15722883-G-T

42148600-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15722855-T-A

42148705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15722764-A-G

42148811-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15722684-C-G

42148855-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15722638-C-G

42148886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15722607-G-T

42149075-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15722387-T-A

42149119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15722345-G-A

42149119-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15722345-G-C

42149262-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15722203-T-A

42149290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15722186-A-G

42149347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15722130-A-G

http://identifiers.org/hco/7/GRCh38#42149449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15722047-C-A

42149566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15721938-C-T

42149576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15721928-T-C

42150119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 15721442-T-C

42150237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15721322-T-C

42150730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15720853-A-G

42150758-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15720828-C-G

42150776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15720810-C-T

42150795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15720787-T-C

42151042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 15720591-T-C

http://identifiers.org/hco/7/GRCh38#42151329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15720321-C-A

42151344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 15720306-G-T

42151390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 15720261-A-G

http://identifiers.org/hco/7/GRCh38#42151442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15720209-C-A

42151539-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 15720112-G-T

42151773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 15719883-G-A

http://identifiers.org/hco/7/GRCh38#42151813-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15719841-A-C

42151864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 15719791-G-T

http://identifiers.org/hco/7/GRCh38#42151882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15719776-C-A

42151882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 15719776-C-T

42152103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 15719615-G-T

http://identifiers.org/hco/7/GRCh38#42152299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15719420-C-A

42152299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 15719420-C-T

42152465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15719185-C-T

42152485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15719151-T-C

42153546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15718084-G-T

42153970-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15717671-T-A

http://identifiers.org/hco/7/GRCh38#42154260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15717419-C-A

42154260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15717419-C-T

42154283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15717395-C-T

42154741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15716983-A-G

42155091-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15716641-C-G

42155728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15716365-G-A

42156002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15716106-A-G

42156745-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15715424-C-G

42156745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15715424-C-T

42156746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15715423-G-A

42156746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15715423-G-T

42156925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15713416-T-C

42157247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15713103-T-C

42157247-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15713103-T-G

42157615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15711556-G-A

42158288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15711064-C-T

42159304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15709816-T-C

42159432-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15709711-T-A

42159482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15709670-A-G

42159498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15709655-G-A

42159721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15709458-A-G

42159948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15709237-T-C

42160026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15709160-G-A

42160026-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15709160-G-C

42160026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15709160-G-T

42161728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron_variant, undefined
orthologous variants: 15707702-T-C

42161943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15707510-T-C

42161968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15707485-A-G

42162287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15706803-G-A

http://identifiers.org/hco/7/GRCh38#42162300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15706790-C-A

42162376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15706729-T-C

42162391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15706714-A-G

42162391-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15706714-A-T

42165452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15702863-T-C

42165917-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15702447-T-A

42165917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15702447-T-C

42165990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15702373-T-C

42166033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15702349-A-G

42166065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15702319-A-G

http://identifiers.org/hco/7/GRCh38#42166441-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15702017-A-C

42166597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15701880-G-A

http://identifiers.org/hco/7/GRCh38#42167407-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15701492-A-C

42167560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15701355-A-G

42167590-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15701325-T-G

42167675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15701222-T-C

42168001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15700909-G-A

42168003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15700907-T-C

42168033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15700878-C-T

42168336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15700595-G-A

42170878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15699019-C-T

42170959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15698938-T-C

42171024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15698875-G-A

http://identifiers.org/hco/7/GRCh38#42171151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15698806-C-A

42171160-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15698797-A-T

http://identifiers.org/hco/7/GRCh38#42171298-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15698658-A-C

42171328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15698626-A-G

42171335-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15698619-G-C

42171347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15698604-T-C

42171502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15698453-T-C

42171660-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15698350-G-C

42171669-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15698335-C-G

42171980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15698062-G-A

42171981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15698061-G-A

42172007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15698032-G-A

42172019-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15698020-C-G

http://identifiers.org/hco/7/GRCh38#42172357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15697647-C-A

42172357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15697647-C-T

42172385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15697602-T-C

42172601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron_variant, missense_variant, synonymous_variant
orthologous variants: 15697357-G-A

42172684-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, splice_region_variant
orthologous variants: 15697254-T-G

http://identifiers.org/hco/7/GRCh38#42172755-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15697183-A-C

42173086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15696862-G-A

42173273-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15696677-A-T

42173631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15696340-T-C

42173752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15696231-A-G

42173760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15696223-T-C

http://identifiers.org/hco/7/GRCh38#42173762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15696221-C-A

42174349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15695568-C-T

42174449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15695486-C-T

42174557-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15695379-T-G

42174689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15695252-G-A

42174896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15695056-G-A

http://identifiers.org/hco/7/GRCh38#42175197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15694804-C-A

42175197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15694804-C-T

42176079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15694255-T-C

42176320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15694039-C-T

42176457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15693929-C-T

http://identifiers.org/hco/7/GRCh38#42176523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15693854-C-A

42176972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15693512-A-G

42177257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15693278-C-T

42177440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15693021-A-G

42178228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15691746-G-A

42178243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15691731-T-C

42178244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15691730-G-A

42178300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15691666-A-G

42178371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15691594-G-A

42178436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15691533-T-C

42178581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15691393-G-A

42181686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15688887-T-C

42181848-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15688735-A-T

42181956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15688634-T-C

42183316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15687942-G-T

42183341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15687917-G-A

42183448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15687816-C-T

42183520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15687745-G-A

42183689-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15687512-T-A

42183708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15687493-C-T

42183760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15687431-G-A

http://identifiers.org/hco/7/GRCh38#42183802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15687396-C-A

42183858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15687346-C-T

42183928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15687290-A-G

42184033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15687171-G-A

42184033-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15687171-G-C

42184084-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15687126-C-G

42184497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15686733-C-T

42184933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15686516-T-C

42185093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15686361-G-A

42185093-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15686361-G-C

42185297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15686089-T-C

42185825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15685806-A-G

42186691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15684823-A-G

42186696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15684818-T-C

42186731-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15684803-G-C

42187505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15684279-C-T

42187718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15684073-A-G

42187880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15684014-G-A

42187987-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15683921-A-T

42188030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15683863-A-G

42188578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15683333-A-G

42188590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15683321-A-G

42188644-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15683256-A-T

http://identifiers.org/hco/7/GRCh38#42188645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15683255-C-A

42188645-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15683255-C-G

42188645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15683255-C-T

42188653-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15683247-T-G

42188695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15683207-G-T

42188721-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15683175-G-C

42189629-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15682329-C-G

42189734-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15682218-T-A

42190021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15681921-G-A

http://identifiers.org/hco/7/GRCh38#42190056-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15681893-A-C

42190125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15681825-A-G

42190320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15681644-G-A

42190347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15681630-C-T

42190481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15681517-T-C

42190575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15681424-T-C

42191019-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15681108-A-T

42191045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15681081-C-T

42191075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15681052-T-C

42191086-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15681041-G-T

42191278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15680857-T-C

42191842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15680702-T-C

42191901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15680650-G-A

42192097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15680470-C-T

42192268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15680298-A-G

42192803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15679866-A-G

42193424-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15679291-T-A

42193424-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15679291-T-G

42193617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15679084-G-A

42193617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15679084-G-T

42195916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15676869-T-C

http://identifiers.org/hco/7/GRCh38#42196200-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15676587-A-C

42196499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15676287-C-T

42196717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15676083-G-A

42196947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15675860-G-A

42196987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15675820-T-C

42197028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15675782-T-C

42197111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15675725-G-A

42197241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15675598-C-T

42197501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15675334-T-C

http://identifiers.org/hco/7/GRCh38#42197740-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15675120-A-C

42197872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15675016-C-T

42198504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15673787-G-A

42198691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15673559-T-C

42198771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15673483-T-C

42198935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15673298-T-C

42198956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15673279-A-G

42199042-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15673194-C-G

42199087-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15673150-T-A

42199155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15673085-C-T

42204075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15670033-G-A

42204305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15669832-C-T

http://identifiers.org/hco/7/GRCh38#42204340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15669796-C-A

42204426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15669689-T-C

42204468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15669643-T-C

42204483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15669629-G-A

42204848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15669280-C-T

42205433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15668806-C-T

42205548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15668728-G-A

42205592-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15668682-T-G

42205701-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15668587-T-A

42205701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15668587-T-C

42205730-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15668558-G-C

http://identifiers.org/hco/7/GRCh38#42205758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15668531-C-A

42205758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15668531-C-T

42205900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15668382-C-T

42205901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15668381-G-A

42206337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15668291-G-A

42206370-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15668261-T-A

42206450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15668184-T-C

42206594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15668057-A-G

42206932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15667704-G-A

42207003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15667633-C-T

http://identifiers.org/hco/7/GRCh38#42207060-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15667586-A-C

42207060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15667586-A-G

42207063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15667583-C-T

42207310-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15667344-G-C

42207322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15667332-T-C

42207467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15667236-T-C

42207543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15667167-T-C

http://identifiers.org/hco/7/GRCh38#42207717-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15666994-A-C

42208319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15666483-C-T

42208426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15666402-G-A

42208463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15666363-C-T

42208517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15666309-C-T

http://identifiers.org/hco/7/GRCh38#42208652-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15666172-A-C

42208951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15665905-T-C

42209436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15665732-A-G

42209741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15665440-C-T

42209849-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15665373-T-A

42209849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15665373-T-C

42210141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15665161-A-G

42210156-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15665148-T-G

http://identifiers.org/hco/7/GRCh38#42211558-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15663374-A-C

42211603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15663338-T-C

42211701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15663240-G-A

42211729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15663214-T-C

42211848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15663070-G-A

42211874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15663043-A-G

42212009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15662914-A-G

42212027-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15662902-C-G

42212076-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15662848-G-C

42212302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15662659-A-G

42212467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15662514-A-G

42212484-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15662500-T-G

42212542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15662445-G-A

42212678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15662306-C-T

42212817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron_variant, undefined
orthologous variants: 15662167-C-T

42212966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron_variant, undefined
orthologous variants: 15662024-C-T

42213107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron_variant, undefined
orthologous variants: 15661898-C-T

42213271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15661713-T-C

42213294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15661690-A-G

42213354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15661635-G-A

42213372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15661620-T-C

42213382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15661610-T-C

42213915-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15661080-G-C

http://identifiers.org/hco/7/GRCh38#42214468-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15660539-A-C

42214468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15660539-A-G

42214845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15660147-G-A

42214845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15660147-G-T

42214896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15660096-G-A

http://identifiers.org/hco/7/GRCh38#42214897-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15660095-A-C

42214916-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15660078-T-A

42215015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15659986-C-T

42215025-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15659978-A-T

42215055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15659961-G-A

42215066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15659954-A-G

42215391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15659652-G-A

42215510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15659535-G-A

42215513-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15659532-T-A

42215513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15659532-T-C

42215636-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15659410-T-A

42215636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15659410-T-C

42216015-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15658925-C-G

42216112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15658841-G-A

42216112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15658841-G-T

http://identifiers.org/hco/7/GRCh38#42216225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15658710-C-A

42216290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15658638-G-A

42216290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15658638-G-T

42216372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15658563-G-A

42216407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15658529-C-T

42216473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15658413-C-T

42216475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15658411-T-C

42216582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15658310-G-A

42216582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15658310-G-T

42216730-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15658183-A-T

42216840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15658067-T-C

42216908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15658045-C-T

42216992-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15657955-G-C

42217037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15657912-C-T

42217041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15657908-T-C

42217173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15657790-G-A

42217188-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15657781-G-C

42217204-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15657763-A-T

42217252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15657738-A-G

42217273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15657716-G-A

http://identifiers.org/hco/7/GRCh38#42217554-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15657435-A-C

42217646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15657329-G-T

42217800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15657183-T-C

http://identifiers.org/hco/7/GRCh38#42217806-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15657177-A-C

42217813-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15657170-T-G

http://identifiers.org/hco/7/GRCh38#42217848-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15657129-A-C

42217848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15657129-A-G

42217858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15657115-T-C

42218108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15656907-G-A

42218340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15656704-A-G

http://identifiers.org/hco/7/GRCh38#42218466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15656595-C-A

42218466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15656595-C-T

42218650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15656460-T-C

42219164-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15655941-T-A

http://identifiers.org/hco/7/GRCh38#42220185-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15655249-A-C

42220190-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 15655243-A-T

42220362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 15655093-G-A

42220520-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 15654952-T-G

42220778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15654581-G-A

42220961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15654403-G-A

42220982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15654382-T-C

42221080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15654285-C-T

42221171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15654197-G-A

42221225-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15654144-C-G

42221377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15653993-T-C

42221377-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15653993-T-G

42221826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 15653691-C-T

42221890-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 15653628-A-T

42221916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 15653594-C-T

42222228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 15653444-T-C

42222286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 15653437-G-A

42222440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 15653350-T-C

42222469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 15653323-C-T

42222665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 15653155-A-G

42222694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 15653128-A-G

42222763-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 15653078-G-C

42222763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 15653078-G-T

42223068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 15652808-G-T

http://identifiers.org/hco/7/GRCh38#42223083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15652793-C-A

42223083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 15652793-C-T

42223222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: missense variant
orthologous variants: 15652655-G-A

42223222-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: missense variant
orthologous variants: 15652655-G-C

42223323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15652555-T-C

42223323-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15652555-T-G

42223894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15651792-T-C

42224130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15651556-G-A

42224204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15651489-G-A

42224244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15651449-A-G

42224266-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15651427-A-T

42224318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15651376-G-A

42224402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15651293-A-G

42224455-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15651261-C-G

42224593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15651137-C-T

42224828-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron_variant, undefined
orthologous variants: 15650960-A-T

42224944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15650894-A-G

42225033-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15650827-G-C

42225039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15650821-G-A

42225043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15650817-C-T

42225076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15650786-G-A

42225229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15650588-T-C

http://identifiers.org/hco/7/GRCh38#42225705-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15650067-A-C

42225887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15649889-C-T

42226228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15649603-G-A

42226248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15649580-G-A

http://identifiers.org/hco/7/GRCh38#42226339-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15649533-A-C

42226339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15649533-A-G

42226339-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15649533-A-T

42226565-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15649330-T-A

42226788-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15649095-G-C

42226972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15648970-G-A

42227091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15648868-T-C

42227140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15648819-T-C

http://identifiers.org/hco/7/GRCh38#42227589-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15648343-A-C

42227728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15648225-A-G

http://identifiers.org/hco/7/GRCh38#42227767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15648181-C-A

42228812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15647471-C-T

42228901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15647397-G-A

42228965-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15646647-G-C

42228988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15646627-C-T

42229028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15646587-T-C

42229085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15646530-A-G

http://identifiers.org/hco/7/GRCh38#42229115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15646492-C-A

42229170-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15646440-G-C

42229523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15646038-A-G

42229598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15645950-G-A

42230058-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15645496-C-G

42230119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15645454-G-A

42230119-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15645454-G-C

42230119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15645454-G-T

42230554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15645043-T-C

42230709-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15644907-T-G

42230739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15644877-T-C

42231833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15643718-G-A

42232023-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15643576-T-A

42232090-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15643518-A-T

42232481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15643154-T-C

42232999-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15642566-C-G

42233220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15642348-G-A

42233442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15642124-C-T

42233448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15642118-C-T

http://identifiers.org/hco/7/GRCh38#42233705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15641859-C-A

42234036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15641541-T-C

42234161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15641416-G-T

42234639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15640969-G-A

42235706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 15639798-G-A

http://identifiers.org/hco/7/GRCh38#42236091-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15639439-A-C

42236285-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 15639211-T-A

42236285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 15639211-T-C

42236479-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15639011-C-G

42237087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 15638612-G-A

42237087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 15638612-G-T

42237098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 15638601-G-A

42237142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 15638556-G-A

42237142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 15638556-G-T

http://identifiers.org/hco/7/GRCh38#42237623-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15638182-A-C

42237638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15638167-T-C

http://identifiers.org/hco/7/GRCh38#42237697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15638105-C-A

42237697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15638105-C-T

42237715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15638084-G-A

42237715-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15638084-G-T

42237807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15637968-G-A

42237807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15637968-G-T

42238940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15637048-A-G

http://identifiers.org/hco/7/GRCh38#42239641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15636397-C-A

42239706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15636332-A-G

42239809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15636201-T-C

42239973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15636048-A-G

42239973-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15636048-A-T

42240239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15635809-A-G

42240893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15634213-C-T

42240980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15634126-A-G

42241016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15634091-A-G

42241237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15633910-G-A

http://identifiers.org/hco/7/GRCh38#42241268-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15633877-A-C

42241274-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15633871-A-T

42241945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15632374-T-C

42241968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15632350-T-C

42241980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15632338-A-G

42242079-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15632263-T-A

42242079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15632263-T-C

42242085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15632261-A-G

42242151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15632188-T-C

42242252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15632108-T-C

42242283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15632096-G-A

42242293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15632086-G-A

42242484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15631908-C-T

42242572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15631808-G-A

42242635-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15631744-T-G

42242848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15631565-C-T

http://identifiers.org/hco/7/GRCh38#42242897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15631515-C-A

42243370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15631079-C-T

http://identifiers.org/hco/7/GRCh38#42244704-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15627577-A-C

42244734-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15627548-T-A

http://identifiers.org/hco/7/GRCh38#42244821-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15626817-A-C

42244829-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15626809-G-C

42245043-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15626610-A-T

http://identifiers.org/hco/7/GRCh38#42245073-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15626580-A-C

http://identifiers.org/hco/7/GRCh38#42247308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15623934-C-A

42247308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15623934-C-T

42247315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15623927-T-C

42247342-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15623900-T-A

42247542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15623721-A-G

42247568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15623696-G-A

42247774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron_variant, undefined
orthologous variants: 15623519-G-A

42247803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15623483-C-T

42247813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15623473-G-A

http://identifiers.org/hco/7/GRCh38#42247918-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15623389-A-C

42247969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15623337-A-G

42248023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15623288-G-A

http://identifiers.org/hco/7/GRCh38#42248033-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15623278-C-A

42248033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15623278-C-T

http://identifiers.org/hco/7/GRCh38#42248053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15623259-C-A

42248082-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15623229-T-A

42248234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15623051-C-T

42248237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15623048-G-A

42248252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15623033-A-G

42248310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15622976-A-G

http://identifiers.org/hco/7/GRCh38#42248460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#15622826-C-A

42249236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15621959-A-G

42250109-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15621443-A-T

42250118-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15621434-C-G

42251545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15621097-A-G

42251814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15620831-A-G

42251855-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15620788-A-T

42251887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15620756-T-C

42253546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15618973-C-T

42253586-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4319
most severe consequence: intron variant
orthologous variants: 15618933-G-C