1172536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8833131-C-T

1172813-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8832828-C-G

1172813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8832828-C-T

1172871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8832766-T-C

1172962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8832666-G-A

1174650-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8821030-C-G

http://identifiers.org/hco/10/GRCh38#1175188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8820833-C-A

1175221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8820800-G-A

1175250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8820770-T-C

http://identifiers.org/hco/10/GRCh38#1175391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8820603-C-A

1175461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8820534-C-T

1175494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8820496-A-G

1177207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8818921-G-T

1177274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8818826-A-G

1177277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8818823-T-C

http://identifiers.org/hco/10/GRCh38#1177639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#8818453-C-A

1177639-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8818453-C-G

1177639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8818453-C-T

http://identifiers.org/hco/10/GRCh38#1177700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#8818390-C-A

1177742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8818349-G-T

1177783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8818308-G-T

1178022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8818249-G-A

1178022-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8818249-G-T

1178098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8818190-A-G

http://identifiers.org/hco/10/GRCh38#1178109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#8818185-C-A

1178109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8818185-C-T

1178112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8818182-C-T

1178140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8818161-G-A

1178140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8818161-G-T

http://identifiers.org/hco/10/GRCh38#1178148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#8818153-C-A

1178148-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8818153-C-G

1178148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8818153-C-T

1178196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8818102-G-A

1178196-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8818102-G-C

1178196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8818102-G-T

1178241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8818062-A-G

1178241-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8818062-A-T

1178292-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8818027-A-T

http://identifiers.org/hco/10/GRCh38#1178402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#8817933-C-A

1178402-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8817933-C-G

1178442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8817893-T-C

http://identifiers.org/hco/10/GRCh38#1178445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#8817890-C-A

1178445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8817890-C-T

1178486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8817856-G-A

1178486-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8817856-G-C

1178486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8817856-G-T

1178490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8817852-C-T

1178502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8817840-A-G

1178502-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8817840-A-T

1178503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8817839-G-T

http://identifiers.org/hco/10/GRCh38#1178544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#8817792-C-A

1178544-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8817792-C-G

http://identifiers.org/hco/10/GRCh38#1178561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#8817769-C-A

1178561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8817769-C-T

1178562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8817768-T-C

http://identifiers.org/hco/10/GRCh38#1178741-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#8817603-A-C

1178876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8817462-C-T

1178964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8811827-T-C

1179253-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8811536-T-A

1179285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8811503-G-A

1179416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8811370-G-A

1179476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8811311-G-T

1179525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8811261-T-C

1179533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8811253-C-T

1179750-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8811031-G-C

1179976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8810862-C-T

1179977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8810861-G-A

1180080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8810760-G-T

1180081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8810759-T-C

1180109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8810730-G-T

1180123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8810716-G-A

1181061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8809614-A-G

1181086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8809551-C-T

1181105-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8809532-C-G

1181191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8809447-G-T

1181205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8809435-G-A

1181282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8809378-G-T

1181689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8809004-C-T

http://identifiers.org/hco/10/GRCh38#1181859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#8808617-C-A

1181859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8808617-C-T

1181998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8808501-G-T

1182060-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8808436-T-G

1182179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8808290-G-T

1182248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8808219-A-G

1182691-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8807938-G-C

1182691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8807938-G-T

http://identifiers.org/hco/10/GRCh38#1182737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#8807892-C-A

1182737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8807892-C-T

1182831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8807781-G-A

1182831-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8807781-G-C

1182831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8807781-G-T

1182836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8807776-G-T

http://identifiers.org/hco/10/GRCh38#1182965-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#8807664-A-C

1182965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 8807664-A-G

1182965-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 8807664-A-T

1182982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 8807647-G-A

1182982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 8807647-G-T

1183003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 8807625-G-A

1183003-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 8807625-G-T

1183027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 8807598-G-A

1183027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 8807598-G-T

1183028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 8807597-T-C

1183028-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 8807597-T-G

1183041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 8807582-T-C

http://identifiers.org/hco/10/GRCh38#1183062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#8807561-C-A

1183062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 8807561-C-T

1183349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 8807280-G-A

1183350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 8807279-C-T

1183431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8807214-G-A

1184737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8802919-T-C

1184737-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8802919-T-G

http://identifiers.org/hco/10/GRCh38#1184787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8802863-C-A

http://identifiers.org/hco/10/GRCh38#1184836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8802810-C-A

1184966-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 8802680-C-G

1184966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 8802680-C-T

1185090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8802561-G-A

1185175-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8802465-T-G

1185408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8802232-G-A

1185468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8802194-C-T

http://identifiers.org/hco/10/GRCh38#1185755-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8801720-A-C

1185891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8801569-G-A

1186084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8801364-G-A

1186084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8801364-G-T

1186480-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8801000-C-G

1186480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8801000-C-T

1186648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8800255-G-A

1186648-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8800255-G-C

1186648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8800255-G-T

http://identifiers.org/hco/10/GRCh38#1186667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8800234-C-A

1186667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8800234-C-T

1186670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8800231-G-T

http://identifiers.org/hco/10/GRCh38#1186677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8800224-C-A

1186677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8800224-C-T

1186702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8800199-G-A

1186702-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8800199-G-C

1186702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8800199-G-T

1186720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8800181-C-T

1186852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8800091-A-G

1186948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8800005-C-T

1187376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8799564-C-T

1187552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8799380-C-T

1187688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8799217-A-G

1187718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8799187-T-C

http://identifiers.org/hco/10/GRCh38#1187733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8799175-C-A

1187733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8799175-C-T

1187759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8799158-A-G

1188033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8799084-G-A

1188033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8799084-G-T

http://identifiers.org/hco/10/GRCh38#1188039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8799081-C-A

1188039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8799081-C-T

1188137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8799014-G-A

1188137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8799014-G-T

http://identifiers.org/hco/10/GRCh38#1188140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8799011-C-A

1190462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8795296-G-A

1190590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8795187-C-T

1190694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8795080-G-A

1190969-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8794902-C-G

1191288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8794523-C-T

1191358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8794458-T-C

1191902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8793923-G-A

1191917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8793907-C-T

1192164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8793650-C-T

1192469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8793160-T-C

1192493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8793136-C-T

1197310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8791855-C-T

1197507-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8791708-C-G

1197583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8791629-C-T

1197646-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8791571-C-G

1198354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8789522-A-G

1198370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8789506-T-C

1198479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8789381-A-G

1198563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8789297-T-C

1198580-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8789288-A-T

1198602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8789266-C-T

1199836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8782121-T-C

1199910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8782051-G-A

1200013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 8781958-A-G

1200121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 8781850-G-A

1200121-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 8781850-G-C

1200121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 8781850-G-T

1200336-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 8781125-G-T

http://identifiers.org/hco/10/GRCh38#1200513-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8780946-A-C

http://identifiers.org/hco/10/GRCh38#1200726-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8780717-A-C

1200950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8780496-G-A

1200950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8780496-G-T

1200995-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8780449-C-G

1202757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8778969-C-T

1203235-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8778487-A-T

1203247-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8778474-C-G

1208214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8774117-T-C

1210198-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8771791-G-C

1210350-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8771647-C-G

1210478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8771520-C-T

1211493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8769474-G-A

1211695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8769254-A-G

1212010-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8768922-C-G

1212045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8768883-G-A

1212049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8768879-G-A

1212071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8768858-G-A

1212124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8768804-T-C

1212143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8768785-G-A

http://identifiers.org/hco/10/GRCh38#1212152-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8768776-A-C

1212152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8768776-A-G

1212315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8768603-A-G

1212316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8768602-G-A

1212367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8768551-C-T

1212596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8768331-C-T

1212612-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8768315-G-C

http://identifiers.org/hco/10/GRCh38#1212649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8768279-C-A

1212649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8768279-C-T

1213061-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8767958-C-G

1213077-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8767939-T-G

1213100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8767920-T-C

1213119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8767906-G-A

1213132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8767893-T-C

1213179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8767844-G-A

1213198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8767825-A-G

1213236-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8767763-G-C

1213300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8767691-G-A

1213300-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8767691-G-C

1213431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8767554-C-T

1213473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8767516-A-G

http://identifiers.org/hco/10/GRCh38#1213533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8767476-C-A

1213593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8767421-G-A

1213601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8767413-C-T

1213672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8767339-C-T

http://identifiers.org/hco/10/GRCh38#1214607-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8765504-A-C

1214822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8765291-C-T

1216823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8763933-G-T

http://identifiers.org/hco/10/GRCh38#1216832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8763922-C-A

1216832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8763922-C-T

http://identifiers.org/hco/10/GRCh38#1216833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8763921-C-A

1216833-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8763921-C-G

1216843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8763911-T-C

http://identifiers.org/hco/10/GRCh38#1216866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8763896-C-A

1216876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8763886-G-A

1216876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8763886-G-T

1216879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8763883-G-A

1216879-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8763883-G-T

http://identifiers.org/hco/10/GRCh38#1216995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#8763758-C-A

1216995-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 8763758-C-G

1217135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8763616-G-A

1217135-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8763616-G-C

1217143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8763608-G-A

1217143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8763608-G-T

1217193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8763563-G-A

1217193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8763563-G-T

http://identifiers.org/hco/10/GRCh38#1217211-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8763547-A-C

1217211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8763547-A-G

1217260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8763519-A-G

1220535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8761612-G-A

1220535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8761612-G-T

1220630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8761521-T-C

1220690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8761458-T-C

http://identifiers.org/hco/10/GRCh38#1220698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8761455-C-A

1220698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8761455-C-T

1220966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8761245-T-C

1228127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8760308-A-G

1228168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8760267-C-T

1229046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8759037-C-T

1229109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8758977-A-G

1229193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8758909-T-C

http://identifiers.org/hco/10/GRCh38#1229250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8758861-C-A

http://identifiers.org/hco/10/GRCh38#1229445-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8758642-A-C

1229579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8756898-C-T

1229917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8756683-G-A

1230035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8756579-T-C

1230258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8756374-G-A

1230481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8756146-C-T

http://identifiers.org/hco/10/GRCh38#1231010-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8755620-A-C

1231113-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8755526-T-G

1231426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8755338-G-A

1233285-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8752169-C-G

1233412-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8752041-G-C

1233504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8751944-C-T

1233640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8751824-A-G

1233655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8751804-G-A

http://identifiers.org/hco/10/GRCh38#1233780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#8751679-C-A

1233780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 8751679-C-T

1233825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 8751634-T-C

http://identifiers.org/hco/10/GRCh38#1233871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8751588-C-A

1233935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8751526-G-A

1233935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8751526-G-T

http://identifiers.org/hco/10/GRCh38#1233965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8751492-C-A

1233965-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8751492-C-G

1233965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8751492-C-T

1233980-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8751477-T-A

1233980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8751477-T-C

1233980-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8751477-T-G

1240386-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 8750610-C-G

1240386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 8750610-C-T

1240392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8750604-C-T

1240479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8750506-C-T

http://identifiers.org/hco/10/GRCh38#1240540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8750449-C-A

1240540-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8750449-C-G

1240540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8750449-C-T

http://identifiers.org/hco/10/GRCh38#1240547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8750442-C-A

1240547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8750442-C-T

1240555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8750436-A-G

1240564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8750427-T-C

1240607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8750384-A-G

http://identifiers.org/hco/10/GRCh38#1240624-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8750367-A-C

1240624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8750367-A-G

1240624-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8750367-A-T

1240625-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8750366-G-C

http://identifiers.org/hco/10/GRCh38#1240649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8750332-C-A

1240649-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8750332-C-G

1240649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8750332-C-T

1240661-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8750320-T-A

1240661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8750320-T-C

1240666-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8750313-T-A

1240666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8750313-T-C

1240666-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8750313-T-G

1240675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8750304-T-C

http://identifiers.org/hco/10/GRCh38#1240678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8750300-C-A

1240678-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8750300-C-G

1240678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8750300-C-T

1240838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8750163-A-G

1241467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8749826-C-T

1241537-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8749754-G-C

1241539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8749752-C-T

1241563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8749728-A-G

1241889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8748081-T-C

http://identifiers.org/hco/10/GRCh38#1242007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8747974-C-A

1242185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8747768-A-G

1242278-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8747675-T-A

1242278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8747675-T-C

1242942-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8743277-T-G

1243101-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8743147-G-C

1243134-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8743108-T-A

1243216-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8743038-C-G

1243220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8743034-G-T

1243375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8742864-C-T

1243564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8742701-C-T

1243618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8742652-G-T

1243752-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8742455-T-G

1243781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8742426-C-T

1243860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8742366-A-G

1243900-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8742326-C-G

1244282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8741903-G-A

1244431-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8741752-C-G

1244716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8741421-T-C

1244845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8741251-G-A

1244845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8741251-G-T

1245167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8740893-G-A

1251960-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8736569-C-G

http://identifiers.org/hco/10/GRCh38#1251975-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8736554-A-C

1252276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8736275-T-C

1252750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8735822-G-A

1253351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8735269-A-G

1253535-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8735113-T-A

1254984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8735019-C-T

1255018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8734987-C-T

1255521-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8734024-A-T

1255578-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8733967-A-T

1255760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8733800-G-A

1255807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8733752-T-C

1257016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8730925-A-G

1257315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8730562-C-T

1257363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8730517-T-C

1257363-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8730517-T-G

1257370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8730510-C-T

1257727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8730095-G-A

1263213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8729825-A-G

1263536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8729509-A-G

1263755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8728980-C-T

1264065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8728700-G-A

http://identifiers.org/hco/10/GRCh38#1264386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8728407-C-A

1264386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8728407-C-T

1264471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8728329-G-T

1264511-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8728289-T-G

1264601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8728200-T-C

1264602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8728199-A-G

1264644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8728157-C-T

1264684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8728112-C-T

1268495-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8726160-T-G

1268512-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8726143-T-G

1268545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8726111-T-C

1268580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8726082-A-G

1268866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8725780-C-T

1268948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8725698-A-G

1268974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8725670-A-G

http://identifiers.org/hco/10/GRCh38#1269030-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#8725620-A-C

1269030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8725620-A-G

1269248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8725430-C-T

1269410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8725267-A-G

http://identifiers.org/hco/10/GRCh38#1269614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8724407-C-A

1269758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8724311-C-T

1269973-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8724070-T-G

1270068-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8723976-C-G

1270295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8723722-A-G

1270316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8723705-G-A

1270471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8723612-A-G

1270561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8723526-A-G

http://identifiers.org/hco/10/GRCh38#1270653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8723425-C-A

1270653-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8723425-C-G

1270890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8722619-A-G

1270965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8722543-G-A

1271105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8722402-G-A

1271105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8722402-G-T

1271148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8722387-C-T

1271192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8722344-T-C

1271556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8721482-C-T

1271615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8721409-C-T

1271715-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8721244-C-G

1271715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8721244-C-T

1271718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8721240-G-A

1271738-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8721220-C-G

1271760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8721198-C-T

1271771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8721187-C-T

1271896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8721086-C-T

1272434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8720646-C-T

1272467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8720615-C-T

1274765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8715324-C-T

1275321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8714791-T-C

1275386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8714725-G-T

1275389-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8714722-T-G

1275408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8714703-G-T

1278888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8714158-G-A

1278978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8714058-G-A

1280112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8712904-G-A

1280375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8712674-G-A

1280428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8712597-C-T

1281279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8711587-T-C

1281284-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8711582-A-T

1281402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8711475-G-T

1281499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8711387-T-C

1281521-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8711366-T-G

1281543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8711345-G-A

1281833-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-A

1281909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8711041-G-A

1282726-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8702212-C-G

1282743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8702192-T-C

1282878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8701711-G-A

1282879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8701710-A-G

1283284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8700915-T-C

http://identifiers.org/hco/10/GRCh38#1283401-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8700772-A-C

1283401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8700772-A-G

1283437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8700746-G-A

1284319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8700696-G-A

1284333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8700682-G-A

1284335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8700680-C-T

1284519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8700510-G-A

1284630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8700387-A-G

1285153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8699606-G-A

http://identifiers.org/hco/10/GRCh38#1285298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8699459-C-A

1285298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8699459-C-T

1285528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8699220-C-T

1286000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8698750-G-A

1286065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8698684-G-A

1286139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8698632-A-G

1286140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8698631-T-C

1286189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8698580-G-A

http://identifiers.org/hco/10/GRCh38#1286206-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8698551-A-C

1286304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8698428-G-A

1286304-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8698428-G-C

1286327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8698405-T-C

1286375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8698356-A-G

1287244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8695838-G-A

1287244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8695838-G-T

1287900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8695510-G-A

http://identifiers.org/hco/10/GRCh38#1287930-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#8695481-A-C

1288125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8695300-G-A

1288154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8695271-C-T

1288194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8695213-T-C

1288243-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8695164-T-G

1288306-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8695083-C-G

1288306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8695083-C-T

1288358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8695032-A-G

1288394-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8694996-C-G

1288396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8694994-A-G