41748742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67256416-G-T

41748747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67256421-G-T

41749191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67256860-C-T

41749603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67257266-C-T

41749738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67257408-C-T

41750276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67257932-C-T

http://identifiers.org/hco/4/GRCh38#41750440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#67258078-C-A

41750440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67258078-C-T

41750519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67258155-A-G

41750628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67258265-A-G

http://identifiers.org/hco/4/GRCh38#41752911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#67260413-C-A

41752911-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67260413-C-G

41752911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67260413-C-T

41752912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67260414-G-T

41753145-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67260661-C-G

41753159-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67260675-T-G

41753305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67260831-T-C

41753369-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67260894-C-G

41753398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67260920-G-A

41753456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67260983-C-T

41753462-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67260989-T-A

http://identifiers.org/hco/4/GRCh38#41753949-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#67261530-A-C

41754058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67261637-G-A

http://identifiers.org/hco/4/GRCh38#41755968-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#67265349-A-C

41755968-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67265349-A-T

41756039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67265371-G-A

41756329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67265535-T-C

41756638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67265816-A-G

41756638-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67265816-A-T

41756831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67266005-G-A

41756931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67266087-T-C

41757002-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67266154-T-G

41757007-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67266159-G-T

41757085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67266223-T-C

41757086-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67266224-G-T

41757172-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67266264-T-G

41757851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67266831-G-T

41757863-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67266843-G-C

http://identifiers.org/hco/4/GRCh38#41758214-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#67267151-A-C

41758339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67267308-G-A

41758373-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67267337-G-C

41759061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67267638-A-G

41759121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67267694-G-T

41762019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67272346-A-G

41762119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67272444-T-C

41762120-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67272445-G-C

41762228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67272531-G-A

41762268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67272566-G-A

41762271-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67272569-A-T

41762925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67273307-G-T

41764541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67276730-G-A

http://identifiers.org/hco/4/GRCh38#41764646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#67276841-C-A

http://identifiers.org/hco/4/GRCh38#41764725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#67276901-C-A

41764725-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67276901-C-G

41764863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67277030-C-T

41765121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67277707-T-C

41765121-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67277707-T-G

41765207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67277782-T-C

41765207-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67277782-T-G

41765244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67277820-A-G

41765271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67277849-G-A

41765291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67277869-C-T

41765629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67278336-T-C

41765724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67278453-G-A

http://identifiers.org/hco/4/GRCh38#41765866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#67278805-C-A

41765866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67278805-C-T

41765876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67278815-A-G

41766081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67279007-C-T

41766438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67279352-T-C

41767213-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67280748-T-G

41767258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67280793-A-G

41767418-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67280929-C-G

41769635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67284462-A-G

41769730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67284544-G-A

41769792-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67284600-T-G

41769845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67284653-C-T

41769932-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67284742-C-G

41770023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67284844-C-T

http://identifiers.org/hco/4/GRCh38#41770062-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#67284883-A-C

41770077-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67284893-G-C

41771143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67287274-T-C

41771185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67287322-A-G

http://identifiers.org/hco/4/GRCh38#41771209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#67287349-C-A

41773514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67289419-A-G

http://identifiers.org/hco/4/GRCh38#41773985-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#67289770-A-C

41773985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67289770-A-G

41774110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67289898-G-A

41774272-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67290064-T-G

41774436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67290236-C-T

41774473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67290283-G-T

41774632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67290431-C-T

http://identifiers.org/hco/4/GRCh38#41774649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#67290448-C-A

41774972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67290738-C-T

41775101-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67291183-T-G

41775342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67291719-C-T

41780169-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67294709-T-A

41784053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67295981-C-T

41784148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67296067-G-A

41785380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67297228-T-C

41785498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67297354-A-G

41785608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67297455-G-A

41786421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67298289-G-T

41786445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67298313-G-A

41786584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67298449-T-C

41786613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67298476-T-C

41786643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67298499-C-T

41786657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67298513-T-C

41787175-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67298998-G-T

41787217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67299191-C-T

41787269-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67299243-C-G

41787269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67299243-C-T

41787412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67299483-C-T

41787413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67299484-G-A

41787413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67299484-G-T

41787573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67299674-C-T

41787730-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67299812-T-G

41787984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67300056-G-A

41788092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67300162-G-T

41788120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67300180-G-A

41788120-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67300180-G-C

41788120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67300180-G-T

41788196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67300243-G-A

41788570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67300605-T-C

41788635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67300665-C-T

http://identifiers.org/hco/4/GRCh38#41788776-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#67300778-A-C

41788907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67300897-C-T

41788954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67300945-T-C

41788984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67300975-C-T

41789124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67301113-T-C

41789362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67301587-C-T

41789417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67301643-T-C

41789684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67301877-G-T

41789740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67301940-T-C

41793564-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67303192-C-G

41793585-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67303213-A-T

http://identifiers.org/hco/4/GRCh38#41793652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#67303298-C-A

41793652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67303298-C-T

41793710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67303381-C-T

41793775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67303470-A-G

41793949-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67303657-C-G

41793952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67303660-G-A

41794283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: non coding transcript exon variant
orthologous variants: 67304075-T-C

41794295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: non coding transcript exon variant
orthologous variants: 67304087-A-G

http://identifiers.org/hco/4/GRCh38#41794374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#67304147-C-A

41794912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67304606-A-G

41795099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: non coding transcript exon variant
orthologous variants: 67304750-T-C

41795124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: non coding transcript exon variant
orthologous variants: 67304772-G-A

41795134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: non coding transcript exon variant
orthologous variants: 67304782-A-G

41795165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: non coding transcript exon variant
orthologous variants: 67304813-A-G

41795342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67305762-G-T

41795629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67306488-A-G

http://identifiers.org/hco/4/GRCh38#41795870-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#67306731-A-C

41796025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67306878-A-G

41796270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67307120-G-A

41797235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67308133-A-G

41797308-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67308213-T-G

41797341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67308246-T-C

http://identifiers.org/hco/4/GRCh38#41798153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#67308712-C-A

http://identifiers.org/hco/4/GRCh38#41798496-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#67308873-A-C

41798544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67308915-A-G

41798572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67308946-T-C

41799206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67309575-G-T

41799248-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67309617-C-G

41799248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67309617-C-T

41799264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67309633-C-T

41799279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67309648-T-C

41802672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67314285-G-T

41802826-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67314404-T-G

41803599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67315555-C-T

41803622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67315582-G-A

41803693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67315638-G-T

41803704-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67315657-A-T

41803826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67315749-G-T

41803827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67315750-C-T

http://identifiers.org/hco/4/GRCh38#41804276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#67316156-C-A

http://identifiers.org/hco/4/GRCh38#41804284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#67316171-C-A

41804284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67316171-C-T

41804983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67316543-G-T

41805044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67316595-C-T

http://identifiers.org/hco/4/GRCh38#41805101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#67316638-C-A

41805101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67316638-C-T

41805139-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67316674-G-T

41805199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67316720-G-A

41805225-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67316746-T-A

41805653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67317238-A-G

41805705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67317263-G-A

41805967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67317536-G-T

41806030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67317600-C-T

41806040-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67317614-T-G

41806058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67317632-A-G

http://identifiers.org/hco/4/GRCh38#41806087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#67317658-C-A

41806192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67317754-G-A

41806368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67317909-G-T

41806603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67318128-T-C

41806932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67318416-G-A

41807427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67318734-C-T

41807428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67318735-C-T

41807456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67318763-G-A

41807604-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67318906-A-T

41808468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67319160-T-C

41809069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67319717-G-A

41809136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67319788-A-G

41809290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67319928-C-T

41809318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67319942-T-C

41809349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67319967-A-G

41809636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67320228-G-A

41809768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67320366-C-T

41809816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67320423-A-G

41809847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67320454-A-G

41809858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67320465-A-G

41810037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67320616-G-A

41810092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67320647-A-G

41816000-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67326672-T-A

http://identifiers.org/hco/4/GRCh38#41816152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#67326836-C-A

41816192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67328231-C-T

41816222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67328275-C-T

http://identifiers.org/hco/4/GRCh38#41816825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#67328551-C-A

41816825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67328551-C-T

41816880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67328600-A-G

41817077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67328770-G-T

41817211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67328896-G-T

41817403-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67329075-T-G

41817454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67329124-A-G

41817665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67329326-G-A

41817814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67329445-G-A

41817836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67329468-G-A

41817836-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67329468-G-C

41817836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67329468-G-T

http://identifiers.org/hco/4/GRCh38#41819817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#67334046-C-A

41819937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67334155-G-T

41820024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67334242-C-T

41820152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67334369-A-G

41820344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67334558-G-A

41820482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67334696-G-A

41820519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67334730-T-C

41820519-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67334730-T-G

41820639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67334834-C-T

41820686-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67334878-A-T

41820724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67334917-T-C

41820816-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67334999-G-C

41820852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67335023-T-C

41821055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67335331-G-A

41821404-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67335702-G-C

41821518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67335802-T-C

41821591-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67335862-C-G

41821604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67335868-A-G

41821607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67335871-A-G

41821622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67335884-C-T

41821780-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67336044-T-A

41821780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67336044-T-C

41821900-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67336152-G-C

41822330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67336596-T-C

41822367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67336634-G-T

41822420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67336688-C-T

41822428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67336701-C-T

41822674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67336947-A-G

41822700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67336974-A-G

41823081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67337459-G-A

41823222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67337597-G-T

41823362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67337720-T-C

41823372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67337730-G-T

41823391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67337748-A-G

41823404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67337761-C-T

http://identifiers.org/hco/4/GRCh38#41823817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#67338275-C-A

41823871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67338329-T-C

41823887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67338354-G-A

41823920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67338388-T-C

41823928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67338396-A-G

http://identifiers.org/hco/4/GRCh38#41823933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#67338401-C-A

41823933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67338401-C-T

41823969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67338435-G-A

41824006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67338472-G-T

http://identifiers.org/hco/4/GRCh38#41824022-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#67338487-A-C

41824085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67338560-C-T

http://identifiers.org/hco/4/GRCh38#41824115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#67338590-C-A

http://identifiers.org/hco/4/GRCh38#41824204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#67338670-C-A

http://identifiers.org/hco/4/GRCh38#41824268-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#67338732-C-A

41824290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67338755-G-A

http://identifiers.org/hco/4/GRCh38#41824332-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#67338797-A-C

41824412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67338878-G-A

41824616-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67339095-G-C

41824621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67339100-A-G

http://identifiers.org/hco/4/GRCh38#41824734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#67339268-C-A

41824759-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67339292-T-G

41825008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67339509-C-T

41825585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67341214-A-G

41825763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40457
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67341413-T-C