21994200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89212629-G-A

21994200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89212629-G-T

http://identifiers.org/hco/9/GRCh38#21994373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#89212797-C-A

21994373-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89212797-C-G

21994373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89212797-C-T

21994392-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant, undefined
orthologous variants: 89212811-T-A

21994428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89212853-G-A

21994428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89212853-G-T

21994459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89212884-G-A

21994459-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89212884-G-C

21994459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89212884-G-T

http://identifiers.org/hco/9/GRCh38#21994687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#89213033-C-A

21994687-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89213033-C-G

21994687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89213033-C-T

http://identifiers.org/hco/9/GRCh38#21994692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#89213038-C-A

21994692-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89213038-C-G

21994692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89213038-C-T

http://identifiers.org/hco/9/GRCh38#21994693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#89213039-C-A

21994693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89213039-C-T

http://identifiers.org/hco/9/GRCh38#21994760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#89213096-C-A

21994792-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89213117-G-C

21994792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89213117-G-T

21994794-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89213119-T-A

21994794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89213119-T-C

21994794-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89213119-T-G

21995257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89213488-A-G

http://identifiers.org/hco/9/GRCh38#21995637-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#89213654-A-C

21995637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89213654-A-G

21995637-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89213654-A-T

http://identifiers.org/hco/9/GRCh38#21995687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#89213704-C-A

21995702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89213717-A-G

21995940-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89213929-A-T

21995942-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89213931-T-A

21995942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89213931-T-C

http://identifiers.org/hco/9/GRCh38#21996139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#89214138-C-A

21996406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89214400-A-G

http://identifiers.org/hco/9/GRCh38#21998433-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#89214825-A-C

21999735-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89216815-G-C

21999735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89216815-G-T

22000590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89217733-T-C

http://identifiers.org/hco/9/GRCh38#22000854-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#89218005-A-C

22001059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89218189-T-C

22001059-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89218189-T-G

http://identifiers.org/hco/9/GRCh38#22002031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#89219150-C-A

22002031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89219150-C-T

22002174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89219277-G-A

22002184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89219287-G-T

22004115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89223186-A-G

22004228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89223305-G-T

http://identifiers.org/hco/9/GRCh38#22004287-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#89223365-A-C

22004287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89223365-A-G

22004413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89223480-G-A

http://identifiers.org/hco/9/GRCh38#22004490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#89223561-C-A

22004564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89223990-G-A

http://identifiers.org/hco/9/GRCh38#22004629-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#89224054-A-C

22004629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89224054-A-G

22004632-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89224057-C-G

22004714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89224135-T-C

22004726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89224150-T-C

http://identifiers.org/hco/9/GRCh38#22005175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#89224641-C-A

22005175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89224641-C-T

http://identifiers.org/hco/9/GRCh38#22005194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#89224660-C-A

22005194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89224660-C-T

22005287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89224719-A-G

22005304-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89224730-A-T

http://identifiers.org/hco/9/GRCh38#22005323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#89224745-C-A

22005323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89224745-C-T

http://identifiers.org/hco/9/GRCh38#22005386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#89224788-C-A

22005386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89224788-C-T

22005502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89224875-T-C

22005507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89224880-G-A

22005507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89224880-G-T

http://identifiers.org/hco/9/GRCh38#22005576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#89224929-C-A

22005576-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89224929-C-G

22005576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89224929-C-T

22005649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89224989-T-C

22005693-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89225024-G-C

http://identifiers.org/hco/9/GRCh38#22005703-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#89225032-A-C

22005703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89225032-A-G

22005703-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89225032-A-T

22005753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89225081-T-C

22005753-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89225081-T-G

22005788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89225106-G-A

22005788-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89225106-G-C

22005788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89225106-G-T

22005845-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89225161-C-G

http://identifiers.org/hco/9/GRCh38#22005872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#89225196-C-A

22005872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89225196-C-T

22005890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89225214-G-A

22005890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89225214-G-T

22005913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89225237-A-G

22005966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89225269-G-T

22006047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89225351-C-T

22006430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89225694-C-T

22006476-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89225738-C-G

22006476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89225738-C-T

22006552-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89225796-T-G

22007517-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89227724-G-C

http://identifiers.org/hco/9/GRCh38#22007875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#89228033-C-A

22008110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89228218-G-A

http://identifiers.org/hco/9/GRCh38#22008531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#89228539-C-A

22008531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89228539-C-T

22008610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89228727-T-C

22008610-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89228727-T-G

22008619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89228737-G-T

22008665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89228786-G-A

22008665-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89228786-G-C

22008665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89228786-G-T

22008747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89228852-C-T

22008772-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89228877-C-G

22008784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89228889-G-A

http://identifiers.org/hco/9/GRCh38#22008791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#89228896-C-A

22008841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89228946-G-A

22008841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89228946-G-T

22008904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89229009-C-T

22008934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89229036-C-T

22009047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89229095-C-T

http://identifiers.org/hco/9/GRCh38#22009173-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#89229163-A-C

22009173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89229163-A-G

22009173-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89229163-A-T

22009241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89229180-C-T

22009247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89229186-G-T

22009260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89229194-G-A

22009306-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89229212-G-C

22009306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89229212-G-T

http://identifiers.org/hco/9/GRCh38#22009329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#89229236-C-A

22009329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89229236-C-T

http://identifiers.org/hco/9/GRCh38#22009339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#89229246-C-A

22009339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89229246-C-T

http://identifiers.org/hco/9/GRCh38#22009485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#89229387-C-A

22009485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89229387-C-T

22009511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89229408-G-A

22009511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89229408-G-T

22010000-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89229921-A-T

22010150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89230065-A-G

22010151-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89230066-T-A

22010240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89230153-T-C

22010240-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89230153-T-G

22010243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89230156-T-C

22010436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89230334-G-A

22010538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89230433-G-A

22010960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89231756-G-T

22010968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89231767-G-T

22011075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89231866-A-G

22011084-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89231878-G-C

22011478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89232373-A-G

22011499-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89232393-C-G

22011533-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89232425-T-G

22011649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89232534-A-G

22011910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89232759-G-A

22011910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89232759-G-T

22011962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89232808-C-T

22012036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89232876-T-C

22012629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89232925-A-G

22012637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89232933-G-A

22012637-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89232933-G-C

22012637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89232933-G-T

http://identifiers.org/hco/9/GRCh38#22012639-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#89232935-A-C

22012649-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89232945-T-G

22012837-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89233112-T-G

22012865-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89233141-T-A

22012865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89233141-T-C

http://identifiers.org/hco/9/GRCh38#22016870-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#89233573-A-C

22016870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89233573-A-G

22016930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89233651-A-G

22016930-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89233651-A-T

22016945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89233666-C-T

22016947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89233668-G-T

22017027-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89233743-T-A

22017439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89234260-A-G

22031285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89237280-A-G

22031286-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89237281-C-G

22031286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89237281-C-T

22031364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89237350-A-G

22031461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89237448-T-C

22031518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89237509-T-C

22032126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89238088-G-A

http://identifiers.org/hco/9/GRCh38#22032169-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#89238139-A-C

22032169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89238139-A-G

22032237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89238214-T-C

22032391-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89238363-T-G

22032393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89238365-A-G

22032520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89238491-G-A

22032520-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89238491-G-C

22032520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89238491-G-T

22032546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89238508-C-T

22032697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89238625-A-G

22032753-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89238682-C-G

22033263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89238792-T-C

22033339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89238855-A-G

22033571-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89239083-T-G

22033602-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89239114-G-C

22033733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89239244-T-C

22033763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89239276-A-G

22033822-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89239315-C-G

22035549-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89239753-T-A

22035759-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89239954-T-A

22036805-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89240996-G-C

22036976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89241165-T-C

22037575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89241668-C-T

22037773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89241860-G-A

22037790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89241880-T-C

22038083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89242204-A-G

22038177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89242296-C-T

22038303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89242406-C-T

22038457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89242572-G-T

22038682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89242808-C-T

22038686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89242812-C-T

22038747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89243360-G-A

22038778-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89243385-A-T

22038892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89243496-A-G

22038892-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89243496-A-T

22038983-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89243582-C-G

22039415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89244426-A-G

http://identifiers.org/hco/9/GRCh38#22039448-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#89244462-A-C

22040088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89245013-C-T

22040216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89245138-G-T

22040566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89245300-G-T

22040703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89245427-A-G

22040703-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89245427-A-T

22040802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89245524-G-A

22040957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89245672-A-G

22041005-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89245713-A-T

http://identifiers.org/hco/9/GRCh38#22041009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#89245717-C-A

22041024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89245732-G-T

22041130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89245842-G-T

22041439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89245897-C-T

http://identifiers.org/hco/9/GRCh38#22041480-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#89245943-A-C

22041482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89245945-T-C

22041612-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89246050-C-G

22041622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89246060-A-G

22041690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89246121-A-G

22042072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89248856-C-T

22042183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89249322-C-T

22042346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89249493-A-G

22042581-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89249716-C-G

22043285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89250361-G-A

22043307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89250377-T-C

22043584-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89250679-A-T

22043588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89250683-C-T

22044273-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89251844-C-G

22044318-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89251887-T-A

22044576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89253245-A-G

22044577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89253246-T-C

22044586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89253251-G-A

22048628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89254426-A-G

22048682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89254490-G-T

22048954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89254743-C-T

http://identifiers.org/hco/9/GRCh38#22049091-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#89254868-A-C

22049091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89254868-A-G

22049146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: non coding transcript exon variant
orthologous variants: 89254928-G-A

22049146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: non coding transcript exon variant
orthologous variants: 89254928-G-T

http://identifiers.org/hco/9/GRCh38#22049217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#89254987-C-A

22049236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 89255005-A-G

22049291-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89255051-T-A

http://identifiers.org/hco/9/GRCh38#22049295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#89255055-C-A

http://identifiers.org/hco/9/GRCh38#22049322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#89255084-C-A

22049322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89255084-C-T

22049945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89255609-A-G

22050151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89256741-C-T

22050376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89256940-G-A

22050463-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89257032-T-G

22050682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89257226-C-T

22050736-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89257280-T-A

22050741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89257284-T-C

22051208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89257694-A-G

22051208-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89257694-A-T

22051236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89257720-G-A

22051405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89257876-T-C

22051405-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89257876-T-G

22051440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89257911-T-C

22051448-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89257919-T-G

22051494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89257963-G-A

22051556-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89258023-T-G

22051585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89258051-A-G

22051650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89258113-C-T

22051996-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89260432-T-A

22052020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89260456-C-T

22052243-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89260684-C-G

22052243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89260684-C-T

22052364-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89260805-T-G

22052634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89261114-C-T

22052647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89261127-G-T

22052659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89261139-G-A

22052691-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89261171-C-G

22054534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89261646-T-C

http://identifiers.org/hco/9/GRCh38#22054626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#89261738-C-A

http://identifiers.org/hco/9/GRCh38#22055339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#89261897-C-A

22055682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89262431-G-A

22055722-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89262470-G-C

22055874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89262602-G-A

22055992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89262745-C-T

http://identifiers.org/hco/9/GRCh38#22056033-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#89262785-A-C

22056033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89262785-A-G

http://identifiers.org/hco/9/GRCh38#22056502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#89262911-C-A

22056734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89263084-T-C

22056839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89263177-T-C

22056879-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89263216-T-G

http://identifiers.org/hco/9/GRCh38#22056950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#89263284-C-A

22056950-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89263284-C-G

22057022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89263349-G-A

22057027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89263354-A-G

22057178-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89263502-T-A

22057280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89263616-C-T

22057344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89263681-C-T

22057439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89263759-G-A

22057439-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89263759-G-T

22057446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89263766-C-T

22057450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89263770-A-G

22058551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89265200-G-A

22058551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89265200-G-T

http://identifiers.org/hco/9/GRCh38#22058565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#89265214-C-A

22058565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89265214-C-T

22058649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89265290-A-G

22058649-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89265290-A-T

22061159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89265746-G-A

22061217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89265795-G-A

22061440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89265988-G-T

http://identifiers.org/hco/9/GRCh38#22062064-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#89267909-C-A

22062064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89267909-C-T

22062094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89267939-G-T

22062235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89268028-A-G

22062375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89268161-A-G

22062658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89268458-G-A

22062658-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89268458-G-C

22062725-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89268513-C-G

22063086-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89269585-G-C

22063101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89269600-G-A

22063101-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89269600-G-T

22063264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89269728-G-A

22063399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89269848-T-C

22063477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89269957-T-C

22063486-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89269966-T-A

22063776-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89270218-G-C

22063804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89270246-G-A

22063804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89270246-G-T

http://identifiers.org/hco/9/GRCh38#22063830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#89270271-C-A

22063830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89270271-C-T

http://identifiers.org/hco/9/GRCh38#22063856-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#89270290-A-C

22063856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89270290-A-G

22063874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89270308-A-G

22065599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89271975-G-T

22065660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 89272034-A-G

22065660-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 89272034-A-T

22065674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89272048-G-A

22065674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89272048-G-T

22065870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89272172-T-C

22065875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89272177-T-C

22065905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89272207-G-A

22065905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89272207-G-T

22067483-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89274473-T-G

22067721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89274840-T-C

22067836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89274982-G-A

22067849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89274995-A-G

22067968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89275115-T-C

22068129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89275280-A-G

http://identifiers.org/hco/9/GRCh38#22068336-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#89275426-A-C

http://identifiers.org/hco/9/GRCh38#22068380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#89275469-C-A

22068380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89275469-C-T

22073441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89276474-T-C

22073653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89276732-A-G

22073770-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89276848-G-C

22074623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89277490-G-A

22074623-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89277490-G-C

22074679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89277546-C-T

22075402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89277574-A-G

22075562-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89277718-C-G

http://identifiers.org/hco/9/GRCh38#22075563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#89277719-C-A

22075612-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89277769-C-G

22075688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89277828-G-A

22075724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89277866-G-T

22075792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89277917-G-A

22075818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89277937-T-C

http://identifiers.org/hco/9/GRCh38#22075907-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#89278043-A-C

22075907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89278043-A-G

22075907-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89278043-A-T

22076001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89278129-G-A

22077122-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89278906-C-G

22077300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89279102-G-A

22077338-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89279140-T-G

22077345-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89279147-A-T

22077542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89279334-A-G

22077563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89279355-A-G

22077660-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89279440-T-G

22077683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89279462-A-G

22077758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89279533-A-G

22077763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89279538-A-G

22077781-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89279556-G-C

22077828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89279594-C-T

http://identifiers.org/hco/9/GRCh38#22078470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#89280083-C-A

22078470-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89280083-C-G

22078470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89280083-C-T

22078486-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89280095-C-G

22078932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89280818-C-T

22079174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89281052-G-A

22079529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89281063-G-A

22079697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89281215-G-A

22079910-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89281482-C-G

22080098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89281649-A-G

22080364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89281913-A-G

22080365-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89281914-C-G

22080365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89281914-C-T

22080413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89281957-A-G

22080655-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89282189-A-T

22080885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89282415-T-C

22081274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89283352-G-T

22081278-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89283356-T-A

22081278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89283356-T-C

22081384-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89283473-T-G

22081519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89283623-G-A

22081519-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89283623-G-C

22081544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89283647-A-G

22081610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89283815-C-T

22081715-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89283913-G-C

22081756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89283959-A-G

22081935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89284163-T-C

http://identifiers.org/hco/9/GRCh38#22082091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#89284305-C-A

22082126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89284336-A-G

22082240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89284441-G-A

22082240-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89284441-G-C

22082242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89284443-G-A

http://identifiers.org/hco/9/GRCh38#22082369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#89284535-C-A

http://identifiers.org/hco/9/GRCh38#22082376-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#89284540-A-C

22082376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89284540-A-G

22082435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89284596-A-G

22084183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89291532-G-T

22084202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89291549-G-T

http://identifiers.org/hco/9/GRCh38#22084295-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#89291641-A-C

22084346-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89291691-T-G

22084735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89292463-G-A

22084830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89292557-G-A

22085176-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89292679-T-G

22088435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89293828-G-A

22088435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89293828-G-T

22088606-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89294006-G-C

22088686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89294086-C-T

22088818-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89294216-C-G

http://identifiers.org/hco/9/GRCh38#22088833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#89294230-C-A

22088920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89294317-C-T

22088962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89294359-G-A

22089271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89294641-T-C

22097148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89307703-G-A

22097148-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89307703-G-C

22097257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 89307814-G-T

22097326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89307879-A-G

http://identifiers.org/hco/9/GRCh38#22097347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#89307900-C-A

22097347-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89307900-C-G

22097351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89307904-G-A

22097395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89307961-G-A

22097395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89307961-G-T

22097409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89307975-T-C

22097513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89308083-A-G

22097581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89308152-G-A

22097581-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89308152-G-C

22097581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89308152-G-T

22097583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89308154-A-G

22097837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89309270-C-T

22098393-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89309648-G-C

22098417-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89309663-G-T

http://identifiers.org/hco/9/GRCh38#22098470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#89309717-C-A

22098505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89309749-A-G

22098539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89309787-G-A

22098555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89309803-C-T

22098572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89309820-A-G

22098585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89309830-C-T

22098685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89309912-G-A

22098685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89309912-G-T

http://identifiers.org/hco/9/GRCh38#22098708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#89309947-C-A

22098708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89309947-C-T

22098726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89309959-A-G

22098731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89309964-G-A

22098731-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89309964-G-C

22098743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89309976-T-C

22098826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89310059-A-G

22099031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89310261-G-T

22099349-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89310561-G-C

22099402-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89310603-G-C

22099431-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89310631-T-G

22099452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89310651-G-A

22099678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89311036-A-G

22099746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89311121-G-A

22099765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89311153-A-G

http://identifiers.org/hco/9/GRCh38#22099800-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#89311184-A-C

22099800-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89311184-A-T

22099845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89311221-G-A

22099933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89311229-A-G

22101060-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89313344-A-T

22101118-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89313412-T-A

22101121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89313415-C-T

22101151-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89313440-C-G

22101220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89313497-A-G

22101570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89313820-T-C

22101592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89313876-G-T

22101638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89313987-C-T

22101997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89314349-T-C

22102221-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89314563-C-G

http://identifiers.org/hco/9/GRCh38#22102671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#89315548-C-A

22102672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89315549-C-T

22103108-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89315961-C-G

22103165-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89316017-G-C

22103179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89316031-G-A

22103242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89316083-A-G

22103838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89316638-T-C

22103897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89316697-A-G

22104022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89316806-C-T

22104449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89317180-G-A

22104566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89317293-A-G

22105093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89318047-A-G

22105093-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89318047-A-T

22105130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89318082-G-A

22105182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89318120-G-A

http://identifiers.org/hco/9/GRCh38#22105699-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#89318644-A-C

22106604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89318870-A-G

22106681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89318945-C-T

22106803-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89319051-A-T

22107294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89319665-A-G

22107747-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89320115-G-C

http://identifiers.org/hco/9/GRCh38#22108120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#89320676-C-A

http://identifiers.org/hco/9/GRCh38#22108723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#89321216-C-A

22108795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89321288-T-C

22108988-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89321702-A-T

22109399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89322116-T-C

22109421-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89322137-T-A

22109487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89322191-C-T

22109497-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89322201-T-G

22109594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89322281-G-A

22109747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89322395-A-G

22109849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89322496-C-T

22110260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89322912-A-G

22110260-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89322912-A-T

22110264-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89322916-A-T

22110454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89323251-A-G

22110454-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89323251-A-T

22110458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89323252-A-G

22110678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89323429-T-C

http://identifiers.org/hco/9/GRCh38#22111316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#89324970-C-A

22111316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89324970-C-T

http://identifiers.org/hco/9/GRCh38#22111330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#89324984-C-A

22111598-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89325262-T-G

22111632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89325299-G-A

22111632-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89325299-G-C

22111987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89325519-C-T

22112063-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89325599-A-T

22112989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89326633-G-A

22112994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89326638-G-T

22113047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89326690-A-G

22113266-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89326851-C-G

22113358-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89326935-C-G

22113359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89326936-A-G

http://identifiers.org/hco/9/GRCh38#22113810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#89327464-C-A

http://identifiers.org/hco/9/GRCh38#22113859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#89327514-C-A

22113866-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89327521-T-A

22114184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89328195-T-C

22114315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89328316-C-T

22115286-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89328836-C-G

22115548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89329123-T-C

22115787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89329339-A-G

22116044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89329568-T-C

22116084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89329606-A-G

22116101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89329623-A-G

22116113-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89329635-C-G

22116123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89329645-C-T

22117438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89333210-T-C

22117506-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89333275-G-C

22117506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89333275-G-T

22117618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89333423-T-C

http://identifiers.org/hco/9/GRCh38#22117641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#89333432-C-A

22117641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89333432-C-T

22117649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89333440-G-A

22117649-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89333440-G-C

22117649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89333440-G-T

http://identifiers.org/hco/9/GRCh38#22117667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#89333458-C-A

22117667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89333458-C-T

22117696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89333487-A-G

http://identifiers.org/hco/9/GRCh38#22117697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#89333488-C-A

22117697-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89333488-C-G

22117742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89333533-G-A

http://identifiers.org/hco/9/GRCh38#22117777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#89333568-C-A

22117828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89333616-A-G

22118004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89333762-G-A

22118004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89333762-G-T

22118237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89334042-A-G

22118237-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89334042-A-T

22118238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89334043-C-T

22118350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89334164-T-C

http://identifiers.org/hco/9/GRCh38#22118351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#89334165-C-A

22118356-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89334170-G-C

22118356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89334170-G-T

22118413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89334229-G-A

22118471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89334286-C-T

22118472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89334287-T-C

22118532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89334362-G-A

22118532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89334362-G-T

http://identifiers.org/hco/9/GRCh38#22118593-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#89334420-C-A

http://identifiers.org/hco/9/GRCh38#22118641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#89334460-C-A

22118641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 89334460-C-T

22118849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89334618-T-C

22118865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89334634-G-A

22118865-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89334634-G-C

22118865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89334634-G-T

22118879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89334648-A-G

http://identifiers.org/hco/9/GRCh38#22118950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#89334719-C-A

22119029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89334797-G-T

22119115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89334896-C-T

http://identifiers.org/hco/9/GRCh38#22119168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#89334947-C-A

22119168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89334947-C-T

22119381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89335186-G-T

http://identifiers.org/hco/9/GRCh38#22119514-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#89335313-A-C

22119514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89335313-A-G

22119556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89335351-T-C

22119607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89335399-G-T

22119619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89335411-T-C

http://identifiers.org/hco/9/GRCh38#22119625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#89335417-C-A

22119625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89335417-C-T

22119666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89335459-T-C

22119740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89335530-G-A

22119740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89335530-G-T

22119742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89335532-T-C

http://identifiers.org/hco/9/GRCh38#22119766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#89335557-C-A

http://identifiers.org/hco/9/GRCh38#22119801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#89335592-C-A

22119866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89335655-G-A

22119969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89335727-G-T

22119971-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89335729-C-G

22119971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89335729-C-T

22120306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89336085-C-T

22120316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89336095-G-T

22120340-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89336111-T-G

22120399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89336158-G-T

http://identifiers.org/hco/9/GRCh38#22120474-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#89336210-C-A

22120544-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89336279-C-G

22120562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89336297-G-A

22120625-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89336358-C-G

22120639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89336372-A-G

22120671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89336407-A-G

22120671-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89336407-A-T

22120850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89336534-T-C

22120857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89336540-A-G

http://identifiers.org/hco/9/GRCh38#22120866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#89336550-C-A

22120866-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89336550-C-G

22120869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89336553-G-A

22120967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89336644-A-G

22123663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89339111-A-G

22123689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89339136-A-G

22123689-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89339136-A-T

22123881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89339301-G-A

22123956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89339370-T-C

http://identifiers.org/hco/9/GRCh38#22123968-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#89339382-A-C

22124050-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89339459-C-G

22124050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89339459-C-T

22124148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89339556-T-C

http://identifiers.org/hco/9/GRCh38#22124153-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#89339561-A-C

http://identifiers.org/hco/9/GRCh38#22124415-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#89339802-A-C

22124477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89339875-A-G

22124477-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89339875-A-T

22124516-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89339909-C-G

22124715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89340064-G-A

22124757-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89340106-G-C

22124845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89340196-A-G

22124909-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89340260-T-A

http://identifiers.org/hco/9/GRCh38#22124933-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#89340284-A-C

22125006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89340362-C-T

22125041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89340401-G-A

22125041-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89340401-G-C

22126505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89345990-G-A

22126525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34341
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89346010-T-C