9596359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40155428-G-A

9596435-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40155504-G-C

9596802-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40155845-T-A

9596879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40155900-G-A

9597108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40156126-G-A

9598017-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40156775-T-A

9598017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40156775-T-C

9598017-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40156775-T-G

9598196-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40156954-A-T

http://identifiers.org/hco/6/GRCh38#9598278-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40157032-A-C

9598397-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40157200-A-T

9598577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40157309-G-A

9598956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40157625-T-C

9599117-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40157784-A-T

9599369-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40158168-C-G

9599636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40158408-G-T

9599884-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40158593-G-C

9599884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40158593-G-T

http://identifiers.org/hco/6/GRCh38#9601310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40159707-C-A

9601310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40159707-C-T

9601846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40159937-A-G

9602029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40160133-G-A

9602051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40160162-G-A

http://identifiers.org/hco/6/GRCh38#9602090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40160199-C-A

9602092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40160201-T-C

9602146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40160271-G-A

9602256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40160359-C-T

9602353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40160453-G-T

9602411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40160509-G-A

9602516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40160607-C-T

9602577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40160666-T-C

9602598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40160687-T-C

http://identifiers.org/hco/6/GRCh38#9602656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40160717-C-A

9602706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40160761-G-T

9602709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40160764-T-C

9603120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40161174-G-A

9603685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40161710-A-G

9603938-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40161961-T-A

9604436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40162417-T-C

http://identifiers.org/hco/6/GRCh38#9604734-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40162714-A-C

9604931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40162903-T-C

9605090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40163060-C-T

9605135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40163105-T-C

http://identifiers.org/hco/6/GRCh38#9605152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40163122-C-A

9605437-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40163387-G-C

9605628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40163538-T-C

9605676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40163587-T-C

9605761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40163662-T-C

http://identifiers.org/hco/6/GRCh38#9606971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40164849-C-A

9607245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40165123-A-G

9607557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40165456-A-G

9607601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40165498-G-A

http://identifiers.org/hco/6/GRCh38#9607638-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40165541-A-C

9607638-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40165541-A-T

9607736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40165638-C-T

9608419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40166620-T-C

9608448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40166684-A-G

9608457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40166693-G-A

http://identifiers.org/hco/6/GRCh38#9608498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40166749-C-A

9608790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40167054-T-C

9608826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40167090-T-C

9608874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40167136-G-A

9608906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40167168-C-T

9609237-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40167496-T-G

9609497-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40167762-G-C

9609500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40167765-G-A

9609933-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40168080-T-A

9609940-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40168084-T-A

9610102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40168267-T-C

9610130-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40168295-T-A

9610220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40168377-T-C

9610295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40168435-C-T

9610399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40168542-T-C

9610489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40168634-T-C

9610495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40168648-T-C

9610522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40168675-C-T

http://identifiers.org/hco/6/GRCh38#9610534-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40168687-C-A

9610534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40168687-C-T

9610701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: non coding transcript exon variant
orthologous variants: 40168854-T-C

http://identifiers.org/hco/6/GRCh38#9610778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40168931-C-A

9610788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: non coding transcript exon variant
orthologous variants: 40168941-A-G

9610791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: non coding transcript exon variant
orthologous variants: 40168944-G-A

http://identifiers.org/hco/6/GRCh38#9610793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40168946-C-A

9610793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: non coding transcript exon variant
orthologous variants: 40168946-C-T

http://identifiers.org/hco/6/GRCh38#9610868-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40169009-A-C

9610868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40169009-A-G

9610876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40169017-A-G

http://identifiers.org/hco/6/GRCh38#9610877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40169018-C-A

http://identifiers.org/hco/6/GRCh38#9610957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40169099-C-A

9610963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40169105-T-C

http://identifiers.org/hco/6/GRCh38#9610969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40169111-C-A

9610969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40169111-C-T

9610985-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40169134-T-A

9611176-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40169324-T-G

9611177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40169325-G-A

9611194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40169342-C-T

9611326-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40169474-T-G

9611423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40169567-C-T

9611725-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40169899-C-G

9611725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40169899-C-T

9612042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40170266-G-A

9612739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40171771-A-G

9613157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40171897-A-G

9613214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40171954-C-T

9613313-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40172091-C-G

9613365-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40172139-G-C

9616351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40175425-C-T

9616392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40175464-T-C

9616399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40175471-G-A

9616499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40175586-G-A

9616629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40175727-T-C

http://identifiers.org/hco/6/GRCh38#9616666-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40175767-A-C

9617550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40177021-G-A

9617770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40177234-G-A

9617914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40177361-A-G

9619791-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40178249-T-A

9633291-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40184000-G-C

9633315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40184015-A-G

9633324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40184024-A-G

9633340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40184030-G-A

9633630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40184282-T-C

9633667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40184329-G-A

9633667-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40184329-G-C

http://identifiers.org/hco/6/GRCh38#9633757-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40184415-A-C

9633817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40184475-T-C

9633818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40184476-G-A

9634073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40184679-G-A

http://identifiers.org/hco/6/GRCh38#9634416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40185013-C-A

9634444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40185041-T-C

9634485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40185061-C-T

9634570-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40185146-A-T

9634714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40185299-G-A

9634714-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40185299-G-C

9635154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40185741-T-C

9635202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40185809-T-C

9635376-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40186003-G-C

9635385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40186012-A-G

9635584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40186209-A-G

9635620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40186245-A-G

http://identifiers.org/hco/6/GRCh38#9635737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40186348-C-A

http://identifiers.org/hco/6/GRCh38#9635788-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40186399-A-C

9635798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40186408-G-A

9635821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40186429-T-C

9636008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40186612-A-G

http://identifiers.org/hco/6/GRCh38#9636061-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40186665-A-C

9636116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40186720-T-C

9636169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40186774-C-T

9636212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40186833-T-C

9636763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40187836-T-C

9636792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40187863-G-A

http://identifiers.org/hco/6/GRCh38#9636926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40187996-C-A

9636979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40188048-C-T

9637114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40188183-G-A

9637192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40188258-A-G

9637206-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40188272-A-T

9637287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40188353-A-G

9637471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40188531-C-T

9637572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40188596-A-G

9637622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40188636-G-A

9637660-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40188661-T-G

http://identifiers.org/hco/6/GRCh38#9637707-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40188716-A-C

http://identifiers.org/hco/6/GRCh38#9637784-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40188794-A-C

9645204-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40189664-G-C

9645347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40189834-C-T

9645480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40190075-G-T

9645631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40190173-T-C

9646303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40190434-C-T

9646584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40190713-G-T

9646731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40190859-T-C

http://identifiers.org/hco/6/GRCh38#9647086-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40191201-C-A

9647086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40191201-C-T

http://identifiers.org/hco/6/GRCh38#9647239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40191327-C-A

9647239-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40191327-C-G

9647358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40191468-A-G

9647364-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40191474-T-G

9647845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40192249-C-T

9648453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40192966-T-C

9648865-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40193409-T-A

9648891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40193433-G-A

9648899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40193441-A-G

http://identifiers.org/hco/6/GRCh38#9648932-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40193477-A-C

9648940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40193485-C-T

9649279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40193801-T-C

9649309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40193844-A-G

http://identifiers.org/hco/6/GRCh38#9649378-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40194438-A-C

9649392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40194453-G-T

9649529-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40194591-T-A

9649529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40194591-T-C

9649746-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40194805-T-G

9649815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40194878-C-T

9649920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40194991-C-T

http://identifiers.org/hco/6/GRCh38#9650031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40195101-C-A

9650062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40195132-T-C

9650156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40195222-T-C

9650226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40195293-T-C

9650283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40195339-A-G

9650428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40195477-A-G

9650549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40195679-C-T

9650676-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40196137-G-C

9650831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40196306-G-A

9650831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40196306-G-T

http://identifiers.org/hco/6/GRCh38#9651045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40196493-C-A

9651168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40196617-G-A

9651363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40196767-T-C

9651373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40196777-A-G

9651449-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40196860-A-T

9651762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40197174-G-A

9652009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40197420-T-C

9652073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40197487-T-C

9652083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40197497-G-A

9653506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40200924-G-A

http://identifiers.org/hco/6/GRCh38#9653566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40200986-C-A

http://identifiers.org/hco/6/GRCh38#9653644-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40201057-A-C

9653644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40201057-A-G

http://identifiers.org/hco/6/GRCh38#9653770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40201179-C-A

http://identifiers.org/hco/6/GRCh38#9654015-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40201406-A-C

9654144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40201526-T-C

9654157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40201539-C-T

9654191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40201573-A-G

9654204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40201588-G-A

9654276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40201664-T-C

9654285-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40201673-T-G

9654311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40201696-A-G

9654760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40202381-T-C

9654847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40202455-C-T

9654972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40202581-T-C

9655033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40202641-A-G

9655082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40202681-G-A

9655082-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40202681-G-C

9655082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40202681-G-T

9655123-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40202723-T-G

9655327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40202879-G-T

http://identifiers.org/hco/6/GRCh38#9656336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40211339-C-A

9656336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40211339-C-T

9656339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40211342-C-T

9656373-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40211376-C-G

9656379-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40211382-A-T

9656392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40211396-C-T

9656399-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40211403-T-A

9656457-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40211463-C-G

9656457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40211463-C-T

9656646-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40212042-G-C

http://identifiers.org/hco/6/GRCh38#9656673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40212067-C-A

9656705-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40212090-T-A

9656733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40212118-C-T

9656768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40212145-A-G

9659497-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40214345-T-G

9659561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40214409-T-C

9659648-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40214490-A-T

9659852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40214680-C-T

9660415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40215234-C-T

9660422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40215241-T-C

9660472-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40215287-T-G

9665458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40216958-T-C

9665606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40217103-C-T

9665691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40217174-G-T

9665969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40217451-G-A

9665969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40217451-G-T

9665975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40217486-G-A

9666045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40217556-C-T

9666196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40217621-C-T

9667389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40218537-G-A

9667922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40218888-A-G

9667957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40218923-A-G

9667984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40219889-C-T

9668095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40219987-C-T

9669132-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40220171-A-T

http://identifiers.org/hco/6/GRCh38#9669244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40220281-C-A

9669244-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40220281-C-G

9669569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40220620-C-T

http://identifiers.org/hco/6/GRCh38#9669922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40220952-C-A

9670386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40221415-C-T

9670983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40222004-T-C

9670983-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40222004-T-G

9671099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40222332-A-G

9671246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40222469-G-T

9671358-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40223016-C-G

9671358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40223016-C-T

9671471-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40223118-T-A

9671548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40223187-A-G

9671738-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40223527-C-G

9672042-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40223808-T-A

http://identifiers.org/hco/6/GRCh38#9673012-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40226102-A-C

9673012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40226102-A-G

http://identifiers.org/hco/6/GRCh38#9673027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40226117-C-A

9673027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 40226117-C-T

9673104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: non coding transcript exon variant
orthologous variants: 40226194-G-A

9673297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40226390-T-C

http://identifiers.org/hco/6/GRCh38#9673344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40226441-C-A

9673402-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40226499-C-G

9674287-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40226863-G-C

http://identifiers.org/hco/6/GRCh38#9674374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40226946-C-A

9674374-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40226946-C-G

9674583-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40227778-A-T

9674747-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40227936-G-C

http://identifiers.org/hco/6/GRCh38#9674810-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40227999-A-C

9675353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40228478-T-C

9675671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40228785-G-T

9675924-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40229033-G-T

9675954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40229067-G-A

9675982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40229091-A-G

9677019-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40229608-G-C

9677275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40229969-G-A

9677327-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40230020-C-G

9677415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40230109-A-G

9677447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40230145-G-A

9677598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40230218-C-T

9677686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40230279-T-C

9677740-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40230334-T-G

9677811-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40230402-C-G

9677868-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40230457-T-A

9678039-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40230614-G-C

9678045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40230620-T-C

9681568-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40231376-G-C

9681568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40231376-G-T

9681821-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40231604-T-G

9682172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40231954-C-T

9682279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40232069-G-A

http://identifiers.org/hco/6/GRCh38#9682365-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40232161-A-C

9682461-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40232254-C-G

9682545-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40232303-T-A

9682545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40232303-T-C

9682545-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40232303-T-G

http://identifiers.org/hco/6/GRCh38#9682686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40232446-C-A

9682686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40232446-C-T

9682733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40232491-C-T

9682992-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40232716-T-G

9683181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40232898-G-A

9683181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40232898-G-T

9683259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40232965-A-G

9683261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40232967-C-T

9683334-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40233041-G-C

9683402-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40233096-A-T

9683403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40233097-C-T

9683458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40233138-G-T

9683498-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40233177-C-G

http://identifiers.org/hco/6/GRCh38#9683500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40233179-C-A

9683500-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40233179-C-G

9683500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40233179-C-T

http://identifiers.org/hco/6/GRCh38#9683529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40233208-C-A

9688155-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40234008-T-A

9688437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40234239-C-T

9688706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40234498-T-C

9688750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40234542-T-C

9688891-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40234638-T-A

9689046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40234780-A-G

9689779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40235400-T-C

9689932-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40235541-C-G

http://identifiers.org/hco/6/GRCh38#9689972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40235574-C-A

http://identifiers.org/hco/6/GRCh38#9690099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40235701-C-A

9690144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40235748-A-G

9690282-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40235876-C-G

9690859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40236400-G-T

9690988-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40236542-T-A

9691376-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40236832-C-G

9691741-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40237158-T-A

9692037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40237459-G-A

9692108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40237528-G-A

9692134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40237554-C-T

9692186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40237596-C-T

9692229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40237632-T-C

9692342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40237737-T-C

9692405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40237809-A-G

9692442-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40237863-A-T

9692570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40237989-C-T

http://identifiers.org/hco/6/GRCh38#9692705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40238637-C-A

9692803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40238736-C-T

9695555-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40238827-T-G

9695687-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40238958-A-T

9695794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40239105-C-T

9695973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40239263-A-G

9696185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40239461-C-T

9696239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40239507-G-A

9696341-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40239605-T-A

9696386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40239670-T-C

9696577-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40240058-A-T

http://identifiers.org/hco/6/GRCh38#9696594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40240102-C-A

9696598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40240106-C-T

9696599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40240107-G-A

9696599-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40240107-G-C

9696770-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40240340-A-T

http://identifiers.org/hco/6/GRCh38#9696874-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40240437-C-A

9696874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40240437-C-T

9696880-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40240443-T-A

9696917-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40240473-T-G

9696952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40240504-A-G

9697298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40240905-G-T

9697465-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40241056-C-G

http://identifiers.org/hco/6/GRCh38#9697514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40241112-C-A

9697514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40241112-C-T

9697529-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40241124-A-T

9697566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 40241202-G-A

9697566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 40241202-G-T

9697671-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: non coding transcript exon variant
orthologous variants: 40241298-C-G

9697671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: non coding transcript exon variant
orthologous variants: 40241298-C-T

9697821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40241448-G-T

9698414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40242024-C-T

9698476-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40242086-T-G

9698531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40242132-G-A

9698989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40242567-T-C

9699024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40242601-C-T

9701600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40244220-G-A

9701645-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40244261-C-G

9701645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40244261-C-T

9701654-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40244269-G-C

9701716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40244321-C-T

9701840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40244445-C-T

9702039-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40244655-T-A

9702194-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40244827-A-T

9702257-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40244890-T-G

9704069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40246459-G-A

9704111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40246509-G-A

9704155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40246558-A-G

9704223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40246627-T-C

9704624-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40247478-A-T

9704635-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40247489-T-G

http://identifiers.org/hco/6/GRCh38#9704825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40247679-C-A

9704830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40247684-T-C

9704935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40247789-G-T

9705093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40247956-G-A

9705093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40247956-G-T

http://identifiers.org/hco/6/GRCh38#9705110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40247972-C-A

9705110-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40247972-C-G

9705147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40248008-T-C

9705217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: non coding transcript exon variant
orthologous variants: 40248078-T-C

9705217-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: non coding transcript exon variant
orthologous variants: 40248078-T-G

9705287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: non coding transcript exon variant
orthologous variants: 40248148-G-T

9705335-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: non coding transcript exon variant
orthologous variants: 40248196-A-T

9705521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40248363-G-A

9705521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40248363-G-T

http://identifiers.org/hco/6/GRCh38#9705523-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40248365-A-C

9705523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40248365-A-G

9705523-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40248365-A-T

9705882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40248822-C-T

9705985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40248912-A-G

9705994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40248921-A-G

9706060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40248979-C-T

9706220-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40249128-T-A

9706220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40249128-T-C

9706965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40249611-A-G

9707330-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40250091-T-A

9707414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40250178-T-C

9707549-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40250314-T-A

9707729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40250458-C-T

http://identifiers.org/hco/6/GRCh38#9707748-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40250477-A-C

9707748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40250477-A-G

9707769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: non coding transcript exon variant
orthologous variants: 40250498-G-A

9707769-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: non coding transcript exon variant
orthologous variants: 40250498-G-C

9707769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: non coding transcript exon variant
orthologous variants: 40250498-G-T

9707804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: non coding transcript exon variant
orthologous variants: 40250533-G-A

9707843-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: non coding transcript exon variant
orthologous variants: 40250572-C-G

9707864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: non coding transcript exon variant
orthologous variants: 40250593-G-A

9707864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: non coding transcript exon variant
orthologous variants: 40250593-G-T

http://identifiers.org/hco/6/GRCh38#9708637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40251268-C-A

9708637-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40251268-C-G

9708709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40251330-C-T

9708836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40251463-C-T

9708923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40251560-C-T

9710088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40252049-C-T

9710098-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40252059-T-G

9710389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40252284-T-C

http://identifiers.org/hco/6/GRCh38#9710596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40252628-C-A

9710780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40252794-A-G

http://identifiers.org/hco/6/GRCh38#9710943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40252943-C-A

9710943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40252943-C-T

9711478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40253436-G-A

9711587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40253524-G-T

9711639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40253575-A-G

9711750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40253680-T-C

9711772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40253702-G-A

9711808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40253738-A-G

9712113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40254027-C-T

9712390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40254567-C-T

http://identifiers.org/hco/6/GRCh38#9712463-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40254683-A-C

http://identifiers.org/hco/6/GRCh38#9712473-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40254692-A-C

9712632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40254840-A-G

9712724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40254923-G-T

9712957-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40255138-G-C

9712957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40255138-G-T

9712969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40255150-G-A

http://identifiers.org/hco/6/GRCh38#9713074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40255245-C-A

9713299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40255432-C-T

9715929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40258131-G-A

9716019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40258218-T-C

9716141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40258332-G-A

9716235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40258413-T-C

9716795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40258968-C-T

http://identifiers.org/hco/6/GRCh38#9716799-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40258972-A-C

9717083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40259246-T-C

9717327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40259484-C-T

9717352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40259508-G-A

9717352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40259508-G-T

9717366-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40259520-C-G

http://identifiers.org/hco/6/GRCh38#9717451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40259605-C-A

9717587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40259746-C-T

9717742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40259858-C-T

9718154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40260414-G-A

http://identifiers.org/hco/6/GRCh38#9719169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40260800-C-A

9719195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40260826-G-A

9719195-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40260826-G-C

9719399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40261014-C-T

9719522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40261141-T-C

9719624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40261243-A-G

9719811-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40261412-T-A

9719811-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40261412-T-G

9731313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40264223-G-A

9731532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40264456-T-C

9731570-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40264496-G-C

9731570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40264496-G-T

9731775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40264718-T-C

9731802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40264733-C-T

9731888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40264817-G-A

9731888-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40264817-G-C

9731952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40264883-C-T

9732021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40264956-C-T

9732067-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40264995-T-G

http://identifiers.org/hco/6/GRCh38#9732556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40266299-C-A

9733006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40266732-G-A

http://identifiers.org/hco/6/GRCh38#9733024-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40266750-A-C

http://identifiers.org/hco/6/GRCh38#9733038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40266764-C-A

9733141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40266866-C-T

9733198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40266922-G-A

9733440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40267763-A-G

9733528-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40267846-G-C

9733528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40267846-G-T

9733574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40268041-T-C

9733591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40268059-T-C

9733650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40268117-C-T

9733739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40268288-T-C

9733826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40268408-G-A

9734215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40268783-T-C

9734248-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40268816-G-C

9734248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40268816-G-T

9734273-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40268876-G-C

9734384-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40269004-T-A

9734437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40269057-C-T

9734462-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40269080-A-T

9734777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40269590-A-G

9734901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40270594-G-T

9735083-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40270942-T-A

9735085-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40270944-C-G

9735265-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40271134-C-G

9735517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40271373-A-G

http://identifiers.org/hco/6/GRCh38#9735581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40271434-C-A

9735581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40271434-C-T

9735582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40271435-G-A

9735593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40271442-A-G

9735680-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40271529-A-T

9735747-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40271589-T-A

9735747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40271589-T-C

9735852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40271685-T-C

9735906-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40271734-T-A

9735922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40271747-T-C

9736035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40271860-G-A

9736035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40271860-G-T

9736068-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40271893-A-T

9736092-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40271918-G-C

9736100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40271926-C-T

9736135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40271972-G-A

9744512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40273363-C-T

9744517-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40273368-G-C

http://identifiers.org/hco/6/GRCh38#9744545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40273404-C-A

http://identifiers.org/hco/6/GRCh38#9744656-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40273500-A-C

http://identifiers.org/hco/6/GRCh38#9744755-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40273584-A-C

9744755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40273584-A-G

9744829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40273642-G-A

9744829-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40273642-G-C

9744843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40273656-G-T

http://identifiers.org/hco/6/GRCh38#9745048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40273835-C-A

http://identifiers.org/hco/6/GRCh38#9745207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40274022-C-A

9745373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40274180-C-T

9745462-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40274259-T-G

9745644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40274447-A-G

9745761-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40274562-A-T

9745847-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40274638-T-A

9745847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40274638-T-C

9745918-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40274706-C-G

9745964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40274754-T-C

9746028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40274819-T-C

9746042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40274831-T-C

9746063-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40274852-T-G

http://identifiers.org/hco/6/GRCh38#9746487-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40275118-A-C

9746503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40275138-T-C

9746604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40275235-T-C

9746629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40275259-G-T

9746638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40275268-C-T

9746650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40275280-G-A

9746713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40275344-G-A

9746815-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40275436-T-A

9746815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40275436-T-C

9746815-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40275436-T-G

9746890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40275495-A-G

http://identifiers.org/hco/6/GRCh38#9747042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40275644-C-A

9747075-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40275676-G-C

9747094-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40275692-G-C

http://identifiers.org/hco/6/GRCh38#9747237-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40275840-A-C

http://identifiers.org/hco/6/GRCh38#9747434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40276043-C-A

9747434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40276043-C-T

9747454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40276067-A-G

9748043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40276669-C-T

9748143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40276759-G-A

9749129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40277884-C-T

9749188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40277927-C-T

9749255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40277985-T-C

http://identifiers.org/hco/6/GRCh38#9749307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40278024-C-A

9749307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40278024-C-T

9749450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40278156-T-C

9749450-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40278156-T-G

9749648-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40278353-G-C

9749967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40278687-C-T

9750021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40278741-G-A

9750032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40278757-C-T

9750164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40278889-A-G

http://identifiers.org/hco/6/GRCh38#9750281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40279013-C-A

9750281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40279013-C-T

http://identifiers.org/hco/6/GRCh38#9750314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40279046-C-A

9750314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40279046-C-T

9750384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40279109-A-G

http://identifiers.org/hco/6/GRCh38#9750571-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40279266-A-C

9750592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40279287-G-T

http://identifiers.org/hco/6/GRCh38#9750895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40279543-C-A

9750897-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40279545-G-C

9750936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40279577-G-T

9750952-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40279593-T-A

http://identifiers.org/hco/6/GRCh38#9751514-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40280445-A-C

http://identifiers.org/hco/6/GRCh38#9751907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40280614-C-A

9751908-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40280615-C-G

9751908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40280615-C-T

9752102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40280794-G-A

http://identifiers.org/hco/6/GRCh38#9752252-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40280986-A-C

9752284-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40281017-C-G

http://identifiers.org/hco/6/GRCh38#9752382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40281108-C-A

9752430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40281172-G-A

9752645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40281383-T-C

9752754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40281484-T-C

9752861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40281591-T-C

9753067-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40281802-T-A

9753095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40281862-A-G

9753166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40281939-A-G

9753252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40282007-C-T

9753253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40282008-G-A

9753273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40282021-T-C

9753301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40282046-T-C

9753393-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40282138-T-A

9753480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40282224-T-C

9754021-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40282837-T-G

9754037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40282856-T-C

9754098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40282918-A-G

9754224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40283027-C-T

9756231-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40283648-C-G

9756447-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40283856-T-A

9756447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40283856-T-C

9756523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40283938-T-C

9756538-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40283953-C-G

9756572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40283986-A-G

9756573-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40283987-G-C

9756789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40284194-T-C

http://identifiers.org/hco/6/GRCh38#9756899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40284310-C-A

9756906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40284317-C-T

http://identifiers.org/hco/6/GRCh38#9756974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40284381-C-A

9757015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40284420-G-T

9757198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40284603-T-C

9757638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40285055-T-C

9757654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40285078-A-G

9757757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40285215-T-C

9758085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40285524-G-A

9758149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40285579-G-A

9758352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40285947-T-C

9758505-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40286095-A-T

9758513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40286103-C-T

9758729-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40286287-C-G

9758729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40286287-C-T

9758779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40286328-C-T

http://identifiers.org/hco/6/GRCh38#9758866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40286409-C-A

9758937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40286479-C-T

9758957-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40286499-G-C

9759289-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40286997-C-G

9759435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40287123-T-C

9759468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40287156-G-T

http://identifiers.org/hco/6/GRCh38#9759586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40287254-C-A

9759758-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40287403-G-C

http://identifiers.org/hco/6/GRCh38#9760202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-A

9760202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

9760287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

9760455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40288175-T-C

9760482-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40288202-C-G

9760511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40288237-G-A

9760511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40288237-G-T

9760513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40288239-A-G

9760523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40288249-A-G

http://identifiers.org/hco/6/GRCh38#9760532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40288258-C-A

9760619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40288307-T-C

9760620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40288308-C-T

http://identifiers.org/hco/6/GRCh38#9760819-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40288697-A-C

9760819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40288697-A-G

9760860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40288741-G-A

9760891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40288770-T-C

9761078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40288942-G-A

http://identifiers.org/hco/6/GRCh38#9761227-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40289079-A-C

9761231-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40289083-G-C

9761296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40289154-C-T

9761301-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40289159-C-G

9761390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40289245-A-G

9761408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40289263-A-G

9761408-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40289263-A-T

9761645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40289481-G-A

9762215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40290044-T-C

9762444-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40290279-T-A

9762912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40291336-C-T

9763122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40291534-C-T

9763156-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40291561-T-A

9763156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40291561-T-C

9763480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40291879-A-G

9763725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40291999-G-A

9763730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40292004-A-G

http://identifiers.org/hco/6/GRCh38#9763875-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40292145-A-C

9764016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40292283-T-C

9764064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40292331-G-A

9764087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40292354-T-C

9764354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40292611-G-A

9764572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40292908-T-C

9764732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40293232-C-T

http://identifiers.org/hco/6/GRCh38#9764796-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40293299-A-C

9764810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40293313-G-A

9764925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40293436-T-C

9764943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40293454-C-T

9765088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40293594-A-G

http://identifiers.org/hco/6/GRCh38#9765117-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40293627-A-C

9765124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40293634-C-T

http://identifiers.org/hco/6/GRCh38#9765138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40293648-C-A

9765167-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40293678-G-C

9767180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40295320-C-T

9767363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40295508-A-G

9768507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40295797-A-G

9768567-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40295858-T-A

9768604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40295909-T-C

9768605-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40295910-T-A

9768606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40295911-G-T

9768740-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40296023-G-C

9768840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40296118-T-C

9768842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40296120-T-C

9768870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40296154-A-G

9768904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40296196-A-G

9768912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40296204-A-G

9768974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: non coding transcript exon variant
orthologous variants: 40296266-T-C

9769004-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: non coding transcript exon variant
orthologous variants: 40296296-T-G

9769039-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: non coding transcript exon variant
orthologous variants: 40296331-T-A

9769039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: non coding transcript exon variant
orthologous variants: 40296331-T-C

9769040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: non coding transcript exon variant
orthologous variants: 40296332-C-T

9769077-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40296369-T-A

9769077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40296369-T-C

9769270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40296535-G-A

9769512-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40296759-G-C

http://identifiers.org/hco/6/GRCh38#9769570-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40296818-A-C

9769570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40296818-A-G

9769601-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40296848-C-G

9769659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40296906-C-T

http://identifiers.org/hco/6/GRCh38#9769816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40297053-C-A

9769834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40297071-G-A

9769834-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40297071-G-C

9770587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40297414-C-T

9770608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40297434-T-C

9770778-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40297609-G-C

9770925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40297837-G-A

9771095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40298104-T-C

9771127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40298132-T-C

9772775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40299340-T-C

9772913-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40299478-T-A

9773250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40299866-T-C

9773424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40300915-G-A

9773424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40300915-G-T

http://identifiers.org/hco/6/GRCh38#9773461-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40300952-A-C

9773503-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40300994-C-G

9774449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40301621-T-C

9775615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40301864-C-T

9775631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40301884-T-C

9775665-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40301918-A-T

http://identifiers.org/hco/6/GRCh38#9775667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40301920-C-A

http://identifiers.org/hco/6/GRCh38#9775715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40301967-C-A

9775715-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40301967-C-G

9775769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40302021-G-T

9775791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40302034-A-G

9775791-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40302034-A-T

9775813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: non coding transcript exon variant
orthologous variants: 40302056-G-T

9775823-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: non coding transcript exon variant
orthologous variants: 40302066-T-G

9782726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40306928-C-T

9782938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40307137-A-G

9782951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40307154-A-G

9783049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40307231-T-C

http://identifiers.org/hco/6/GRCh38#9783162-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40307346-A-C

http://identifiers.org/hco/6/GRCh38#9783258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40307435-C-A

9783435-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40307576-T-A

9783435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40307576-T-C

http://identifiers.org/hco/6/GRCh38#9783486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40307643-C-A

9783532-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40307672-C-G

9783534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40307674-G-A

9783534-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40307674-G-T

9783555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40307695-C-T

9783569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40307714-G-A

9783796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40307954-G-A

http://identifiers.org/hco/6/GRCh38#9783865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40308028-C-A

9783892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40308055-G-A

9783963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40308125-A-G

9784371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40308523-T-C

http://identifiers.org/hco/6/GRCh38#9784705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40308858-C-A

9784742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40308896-T-C

9784853-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40309009-G-C

9784937-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40309093-C-G

9785378-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40309545-T-G

9785468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40309629-T-C

9785495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40309655-T-C

9785564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40309733-A-G

http://identifiers.org/hco/6/GRCh38#9786021-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40310154-A-C

9786149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40310286-A-G

9786151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40310288-T-C

9786409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40310768-T-C

9786617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40310959-C-T

9786724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40310994-G-T

9786837-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40311030-C-G

9786837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40311030-C-T

http://identifiers.org/hco/6/GRCh38#9786990-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40311109-A-C

9786990-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40311109-A-T

9787167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40311289-G-A

9787167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40311289-G-T

9794373-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40319800-C-G

9794416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40319833-A-G

9794416-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40319833-A-T

9794500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40319917-A-G

9794558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40319975-G-A

9794582-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40319999-C-G

9794589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40320006-T-C

9794820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40320260-T-C

9795074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40320516-G-A

9795126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40320612-A-G

9795409-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40320829-T-A

9795616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40321010-T-C

9795650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40321039-G-A

9795826-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40321275-A-T

9795891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40321357-A-G

9796214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40321670-T-C

9796214-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40321670-T-G

http://identifiers.org/hco/6/GRCh38#9796283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40321732-C-A

9796298-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40321747-A-T

9796938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40322050-G-A

9796938-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40322050-G-C

9796938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40322050-G-T

9797023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40322111-T-C

9801271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40324846-C-T

9802256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40325797-T-C

9802304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40325849-T-C

9802338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40325883-T-C

9802341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40325886-T-C

9802455-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40326001-C-G

9802541-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40326080-C-G

9802541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40326080-C-T

9802586-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40326130-G-C

9802606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40326150-G-A

http://identifiers.org/hco/6/GRCh38#9803039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40326559-C-A

9803131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40327218-T-C

9803324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40327392-G-A

9804260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40327736-T-C

9804349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40327827-T-C

9804363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40327841-G-A

9804519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40327982-T-C

9804552-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40328014-T-A

9804709-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40328214-C-G

9804709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40328214-C-T

9804710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40328215-G-A

9804778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40328272-C-T

9804779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40328273-G-A

9804779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40328273-G-T

9804791-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40328285-T-A

9808767-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40328881-G-C

9808771-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40328885-A-T

9808863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40328973-T-C

9809244-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40329328-T-A

9809376-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40329467-T-G

9809438-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40329534-T-A

9809501-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40329620-T-A

9809501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40329620-T-C

9809554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40329687-G-A

9809606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40329776-T-C

9809609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40329779-G-A

9809609-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40329779-G-C

9809658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40329828-G-A

9809725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40329895-A-G

9809884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40330107-A-G

9809895-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40330120-A-T

9809999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40330199-T-C

9810091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40330268-G-A

http://identifiers.org/hco/6/GRCh38#9810117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40330334-C-A

9810153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40330370-C-T

9810243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40330452-G-A

9810324-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40330520-G-C

9810508-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40330665-C-G

9810546-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40330703-G-C

9810571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40330727-G-A

9810598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40330743-A-G

9810624-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40330778-T-A

9816834-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40331353-G-C

9816834-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40331353-G-T

http://identifiers.org/hco/6/GRCh38#9817105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40331569-C-A

9817105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40331569-C-T

9817372-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40331799-G-C

9818050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40332526-G-A

http://identifiers.org/hco/6/GRCh38#9818146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40332626-C-A

9818250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40332741-G-A

9818356-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40332931-T-A

9818356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40332931-T-C

http://identifiers.org/hco/6/GRCh38#9818388-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40332972-A-C

http://identifiers.org/hco/6/GRCh38#9818418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40333002-C-A

9818418-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40333002-C-G

http://identifiers.org/hco/6/GRCh38#9818832-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40333446-A-C

9818877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40333495-T-C

9819045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40333645-T-C

http://identifiers.org/hco/6/GRCh38#9819098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40333697-C-A

9819195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40333920-G-T

9819231-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40333956-A-T

9819236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40333961-G-A

9819236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40333961-G-T

9819318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40334043-C-T

http://identifiers.org/hco/6/GRCh38#9819333-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40334058-A-C

9819333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40334058-A-G

9819455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40334182-G-A

9819455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40334182-G-T

9819635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40334341-A-G

9819659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40334361-T-C

9819741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40334446-G-A

9820135-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40335179-T-A

9820135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40335179-T-C

http://identifiers.org/hco/6/GRCh38#9820146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40335185-C-A

9820146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40335185-C-T

9820148-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40335187-A-T

9820322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40335345-T-C

9820445-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40335468-A-T

9820736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40335744-A-G

9820846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40335857-T-C

9821200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40336287-T-C

9821245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40336333-G-A

9821297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40336564-T-C

9821354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40336682-A-G

9821486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40336823-A-G

9821537-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40336879-T-G

9821612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40336952-G-A

9821925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40337091-G-A

9821925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40337091-G-T

9821932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40337098-A-G

9821938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40337104-G-A

9821971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40337138-A-G

9821982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40337155-G-A

9822062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40337244-T-C

9822070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40337252-C-T

9822073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40337255-T-C

9824380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40339354-T-C

9824643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40339616-G-A

9824660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40339633-G-A

9824891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40339838-T-C

9824979-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40339938-T-A

9824979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40339938-T-C

http://identifiers.org/hco/6/GRCh38#9825124-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40340063-A-C

9825124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40340063-A-G

9825138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40340077-A-G

9825247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40340163-G-A

9825247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40340163-G-T

9825541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40340448-A-G

9825549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40340456-T-C

9825768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40340670-C-T

9825782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40340685-G-A

9825782-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40340685-G-C

9825799-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40340702-C-G

9825871-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40340774-A-T

9825924-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40340834-T-G

9826386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40341330-G-A

9826639-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40341557-T-G

9826782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40341670-G-T

9826840-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40341724-C-G

9826902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40341774-G-T

9827399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40342823-T-C

9827649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40343071-G-A

9828922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40345123-A-G

9829063-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40345256-G-C

9829143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40345325-G-A

9829680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40345843-A-G

9830050-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40346219-T-G

9830060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40346227-A-G

9830737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40352950-A-G

9830749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40352963-G-A

9830761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40352975-A-G

http://identifiers.org/hco/6/GRCh38#9830791-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40352997-A-C

9830877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40353063-G-A

9830885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40353071-A-G

9830967-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40353144-G-C

http://identifiers.org/hco/6/GRCh38#9831013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40353188-C-A

9831042-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40353216-G-C

9831066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40353235-C-T

9831117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40353274-C-T

9831181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40353340-T-C

9831282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40353420-T-C

9831471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40353608-A-G

http://identifiers.org/hco/6/GRCh38#9831564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40353703-C-A

http://identifiers.org/hco/6/GRCh38#9831840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40353972-C-A

9831840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40353972-C-T

http://identifiers.org/hco/6/GRCh38#9832171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40354300-C-A

9832203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40354332-C-T

9832268-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40354399-C-G

9832402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40354592-C-T

9832443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40354633-G-A

9832530-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40354718-C-G

http://identifiers.org/hco/6/GRCh38#9832922-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40355120-A-C

9832950-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40355150-G-C

9832960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40355160-G-A

9832960-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40355160-G-C

9834612-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40355982-T-A

9834714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40356068-C-T

http://identifiers.org/hco/6/GRCh38#9834783-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40356139-A-C

9834837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40356202-T-C

9835063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40356423-G-A

9835284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40356628-G-A

9835429-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40357066-A-T

9835468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40357104-G-A

9835738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40357454-T-C

9835825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40357533-G-A

9835853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40357561-T-C

9836694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40358165-T-C

9836720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40358189-G-A

http://identifiers.org/hco/6/GRCh38#9837215-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40358379-A-C

9837957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40358459-A-G

http://identifiers.org/hco/6/GRCh38#9838012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40358511-C-A

9838037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40358539-A-G

9838131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40358599-T-C

9838138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40358605-T-C

9838244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40358707-C-T

http://identifiers.org/hco/6/GRCh38#9839519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40359210-C-A

9839520-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40359211-A-T

9839597-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40359301-C-G

9839650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40359353-C-T

9839661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40359369-C-T

9839686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40359401-T-C

9839728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40359442-G-A

9839729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40359443-T-C

9840089-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40359862-T-A

9840098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40359874-G-A

9840451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40360295-G-A

9840568-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40360410-A-T

9840583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40360425-T-C

9840622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40360464-T-C

9840899-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40360741-T-G

9840906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40360748-T-C

9841036-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40360873-G-C

9841081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40360898-G-A

9841425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40361183-T-C

9841587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40361328-T-C

http://identifiers.org/hco/6/GRCh38#9841806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40361551-C-A

9841806-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40361551-C-G

http://identifiers.org/hco/6/GRCh38#9841850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40361595-C-A

9842147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40361903-A-G

9842207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40361962-G-A

9842207-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40361962-G-C

http://identifiers.org/hco/6/GRCh38#9842456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40362159-C-A

9842579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40362276-G-T

9842580-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40362277-G-T

9842771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40362552-G-A

http://identifiers.org/hco/6/GRCh38#9842793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40362574-C-A

9842793-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40362574-C-G

9842858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40362594-C-T

9843106-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40363648-T-A

9843124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40363666-A-G

9843191-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40363733-T-G

9843672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40364208-G-T

9843694-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40364230-T-G

http://identifiers.org/hco/6/GRCh38#9843745-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40364278-A-C

http://identifiers.org/hco/6/GRCh38#9844109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40366535-C-A

9844162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40366590-T-C

9844308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40366693-C-T

http://identifiers.org/hco/6/GRCh38#9844353-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40366739-C-A

9844353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40366739-C-T

9844355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40366741-T-C

9844381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40366767-T-C

9844716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40367103-A-G

9845112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40367509-G-A

9845178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40367562-G-A

http://identifiers.org/hco/6/GRCh38#9845281-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40367662-A-C

http://identifiers.org/hco/6/GRCh38#9845414-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40367793-A-C

http://identifiers.org/hco/6/GRCh38#9845415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40367794-C-A

9845415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40367794-C-T

http://identifiers.org/hco/6/GRCh38#9845490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40367888-C-A

9845490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40367888-C-T

9845603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40368017-A-G

http://identifiers.org/hco/6/GRCh38#9845737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40368159-C-A

9845737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40368159-C-T

9845929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40368427-G-A

http://identifiers.org/hco/6/GRCh38#9846137-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40368545-A-C

9846150-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40368551-G-C

9846391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40368706-T-C

9846459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40368774-A-G

9846638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40369027-C-T

http://identifiers.org/hco/6/GRCh38#9846701-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40369118-A-C

9846722-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40369139-G-C

9846869-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40369254-G-C

9846894-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40369279-G-C

9846912-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40369296-C-G

9847021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40369367-G-A

9847182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40369530-C-T

9847275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40369618-C-T

9847292-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40369635-G-C

http://identifiers.org/hco/6/GRCh38#9847319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40369667-C-A

9847397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40369744-C-T

9855559-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40382861-G-C

9855605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40382903-A-G

9855811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40384963-T-C

9855820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40384972-G-T

9856114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40385316-A-G

9856247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40385441-T-C

http://identifiers.org/hco/6/GRCh38#9865119-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40391197-A-C

9865319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40391383-T-C

9865371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40391435-G-T

9865375-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40391439-G-C

9865391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40391455-G-T

9865470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40391535-T-C

9865507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40391603-A-G

9865507-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40391603-A-T

http://identifiers.org/hco/6/GRCh38#9865666-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40391790-C-A

9865693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40391817-C-T

http://identifiers.org/hco/6/GRCh38#9865712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40391836-C-A

9865759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40391912-G-A

9865894-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40392048-T-G

http://identifiers.org/hco/6/GRCh38#9866130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40392290-C-A

9866777-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40392561-T-G

9866860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40392652-G-A

9867073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40393061-G-A

9867345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40393387-G-T

9873422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40394463-T-C

9873434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40394475-T-C

9873679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40394716-G-A

9873772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40394796-G-A

9873772-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40394796-G-C

9873802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40394922-G-A

9873802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40394922-G-T

9873871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40395051-C-T

9873877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40395057-T-C

9873925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40395105-T-C

9874036-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40395204-G-C

9874268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40395602-T-C

9874284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40395615-G-T

9874311-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40395649-A-T

9874326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40395663-T-C

9874569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40396276-T-C

9874579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40396286-G-A

http://identifiers.org/hco/6/GRCh38#9874790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40396492-C-A

9874790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40396492-C-T

9874930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40396651-G-A

9875143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40396851-C-T

9875161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40396869-C-T

9875322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40396986-C-T

9875364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40397028-A-G

9875372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40397036-T-C

9875377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40397041-T-C

9875429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40397091-C-T

9875494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40397158-T-C

9876792-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40398521-T-G

9876809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40398538-T-C

9876943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40398651-C-T

9889159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40401985-C-T

9889312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40402132-A-G

9889313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40402133-A-G

9889506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40402302-G-A

http://identifiers.org/hco/6/GRCh38#9889536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40402332-C-A

9889560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40402356-T-C

http://identifiers.org/hco/6/GRCh38#9889616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40402426-C-A

9889654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40402462-T-C

9889761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40402568-G-A

9889822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40402620-A-G

9890043-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40402837-G-C

9890055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40402849-T-C

9890105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40402930-T-C

9890597-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40403406-T-A

9890639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40403467-A-G

9890728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40403560-G-T

9896020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40404918-G-A

http://identifiers.org/hco/6/GRCh38#9896027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40404925-C-A

9896047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40404945-T-C

http://identifiers.org/hco/6/GRCh38#9896182-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40405046-A-C

9896203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40405069-C-T

9896351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40405202-G-A

9896359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40405210-C-T

9896406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40405259-C-T

http://identifiers.org/hco/6/GRCh38#9896564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40405411-C-A

9896564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40405411-C-T

http://identifiers.org/hco/6/GRCh38#9896779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40405609-C-A

9896779-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40405609-C-G

9896801-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40405631-T-G

9896809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40405639-T-C

9896827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40405657-G-T

9896945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40405768-A-G

9897004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 40405809-C-T

9897046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40405852-T-C

9897110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40405915-C-T

9897397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40406323-C-T

9899262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40408003-G-A

9899337-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40408067-G-C

9899758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40408464-G-T

9899856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40408517-G-A

9900178-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40408771-T-A

9900178-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40408771-T-G

9900304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40408892-T-C

9900356-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40408944-T-G

9900358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40408946-T-C

9900380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40408971-C-T

9900391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40408982-G-A

9900568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40409158-T-C

9900594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40409186-G-T

9900824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40409387-G-A

9900828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40409391-T-C

9900984-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40409520-G-C

9901035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40409567-G-A

http://identifiers.org/hco/6/GRCh38#9901097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40409628-C-A

9901103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40409634-C-T

9901155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40409686-G-A

9907477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40412999-A-G

9907493-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40413014-A-T

9907598-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40413106-T-G

9907706-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40413276-T-G

9907922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40413493-C-T

9907968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40413541-A-G

9908005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40413573-T-C

http://identifiers.org/hco/6/GRCh38#9908398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40416918-C-A

9908398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40416918-C-T

http://identifiers.org/hco/6/GRCh38#9908417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40416937-C-A

9908439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40416958-G-A

9908439-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40416958-G-T

9908454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40416973-C-T

http://identifiers.org/hco/6/GRCh38#9908487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40417006-C-A

9908487-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40417006-C-G

9908487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40417006-C-T

9909345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40418202-A-G

9909391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40418248-T-C

9909483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40418319-C-T

9909542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40418380-G-T

9909549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40418387-A-G

9909558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40418396-G-A

9909582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40418420-A-G

9909717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40418545-G-A

9909780-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40418611-T-G

9909881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40418718-G-A

9910106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40418945-G-A

9912073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40420628-T-C

9912227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40420780-T-C

9912419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40420956-A-G

9912605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40421138-C-T

9912814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40421381-G-T

9912957-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40421554-C-G

9912967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40421564-A-G

9913201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40421800-A-G

9914142-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40422589-T-A

9914270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40422709-A-G

http://identifiers.org/hco/6/GRCh38#9914326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40422771-C-A

9914853-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40423105-A-T

9914856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40423108-T-C

9914967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40423219-G-A

9915139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40423369-C-T

9915298-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40423536-T-A

9915522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40423736-T-C

9916422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40424217-T-C

http://identifiers.org/hco/6/GRCh38#9916426-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40424221-C-A

9916621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40424431-T-C

http://identifiers.org/hco/6/GRCh38#9916664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40424475-C-A

http://identifiers.org/hco/6/GRCh38#9916764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40424566-C-A

9916849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40424647-T-C

9916902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40424695-T-C

9917161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40425442-G-A

http://identifiers.org/hco/6/GRCh38#9917590-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40425899-A-C

9917890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40426217-T-C

9918020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40426337-A-G

9918238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40426751-C-T

9918273-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40426785-T-G

9918431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40426915-C-T

9918528-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40427000-C-G

9918609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40427033-G-T

9918637-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40427061-T-A

9918637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40427061-T-C

9918681-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40427101-A-T

9918714-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40427145-A-T

http://identifiers.org/hco/6/GRCh38#9918759-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40427185-A-C

9918892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40427315-T-C

9921912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40428235-G-A

9921912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40428235-G-T

http://identifiers.org/hco/6/GRCh38#9921940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40428263-C-A

9922071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40428380-T-C

9922552-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40429056-T-G

9922698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40429203-G-A

9922834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40429331-C-T

9923487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40429589-C-T

9923499-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40429601-C-G

9923500-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40429602-T-G

9925635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40431101-T-C

9925648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40431113-A-G

9925670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40431135-A-G

9925915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40431374-G-T

9925969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40431422-A-G

9925977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40431430-A-G

9931961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40433060-C-T

9932133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40433211-G-A

9932227-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40433305-C-G

9932279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40433357-T-C

9932341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40433419-T-C

9932634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40433725-C-T

9932650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40433741-A-G

9932650-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40433741-A-T

9932693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40433782-G-A

9932693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40433782-G-T

9932740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40433818-G-T

9932852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: non coding transcript exon variant
orthologous variants: 40433930-T-C

9932924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: non coding transcript exon variant
orthologous variants: 40434002-T-C

9932924-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: non coding transcript exon variant
orthologous variants: 40434002-T-G

http://identifiers.org/hco/6/GRCh38#9932932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40434010-C-A

9932961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40434039-G-A

http://identifiers.org/hco/6/GRCh38#9933163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40434244-C-A

9933163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40434244-C-T

9933660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40434735-T-C

http://identifiers.org/hco/6/GRCh38#9934062-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40435628-A-C

9934084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40435647-A-G

9934230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40435858-G-A

9934286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40435910-T-C

9934286-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40435910-T-G

9934705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40436369-C-T

http://identifiers.org/hco/6/GRCh38#9934708-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40436372-A-C

9934708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40436372-A-G

9935788-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40437919-T-A

9935896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40438006-T-C

9935918-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40438028-T-A

9936165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40438356-C-T

9936738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40438991-G-T

9936789-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40439041-C-G

9936789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40439041-C-T

9936985-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40439234-G-C

9937084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40439332-T-C

9937135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40439384-G-T

9937168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40439416-A-G

9937281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40439550-A-G

9937309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40439582-T-C

9937676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40439957-A-G

9937800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40440055-G-T

9938131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40440322-C-T

http://identifiers.org/hco/6/GRCh38#9938174-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40440367-A-C

9938520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40440690-T-C

9938568-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40440731-C-G

http://identifiers.org/hco/6/GRCh38#9938785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40440945-C-A

9938785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40440945-C-T

9939186-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40441343-A-T

9939231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40441391-A-G

9939635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40441781-A-G

http://identifiers.org/hco/6/GRCh38#9939841-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40441982-A-C

9939932-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40442089-T-G

9939979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40442153-C-T

9940473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40442334-A-G

9940521-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40442380-T-G

9940639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40442451-T-C

9940765-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40442582-G-C

9940907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40442737-T-C

9940946-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40442764-T-G

http://identifiers.org/hco/6/GRCh38#9941005-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21017
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#40442823-A-C