41694222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16197704-G-T

41694549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16197387-G-A

41694557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16197379-G-A

41695009-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16196958-T-A

41695163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16196815-G-A

41695295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16196686-G-A

41695817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16196171-A-G

41695924-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16196069-G-C

41695960-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16196040-G-C

41696952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16195147-C-T

41697040-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16195062-T-G

http://identifiers.org/hco/7/GRCh38#41697365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#16194762-C-A

41697365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16194762-C-T

41697854-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16194309-A-T

41697855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16194308-G-A

41698376-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16193815-A-T

41698449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16193717-T-C

41698470-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16193696-T-A

41698815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16193430-G-A

41698815-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16193430-G-C

41699101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16193156-G-A

41699760-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16192463-T-A

http://identifiers.org/hco/7/GRCh38#41699845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#16192393-C-A

41699845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16192393-C-T

http://identifiers.org/hco/7/GRCh38#41699870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#16192368-C-A

41699870-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16192368-C-G

41699870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16192368-C-T

http://identifiers.org/hco/7/GRCh38#41699873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#16192365-C-A

41699873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16192365-C-T

http://identifiers.org/hco/7/GRCh38#41699898-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#16192340-A-C

41699898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16192340-A-G

41699898-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16192340-A-T

41700680-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16191601-A-T

41700709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16191563-G-T

41700785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16191451-G-A

41700832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16191356-A-G

41701040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16191127-G-T

41701837-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16190276-T-G

41701905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16190208-T-C

41701938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16190175-G-T

41702003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16190118-T-C

http://identifiers.org/hco/7/GRCh38#41702578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#16189540-C-A

41702640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16189478-A-G

http://identifiers.org/hco/7/GRCh38#41703346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#16188775-C-A

http://identifiers.org/hco/7/GRCh38#41703401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#16188720-C-A

41703668-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16188468-C-G

41703756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16188375-T-C

41704027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16188108-G-A

41704054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16188077-T-C

41704240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16187892-T-C

http://identifiers.org/hco/7/GRCh38#41705172-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#16187055-C-A

http://identifiers.org/hco/7/GRCh38#41705262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#16186990-C-A

http://identifiers.org/hco/7/GRCh38#41705536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#16186709-C-A

41705616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 16186644-A-G

41705833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 16186436-C-T

41706570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16185715-T-C

41706626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16185656-G-A

41706696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16185575-G-A

41706696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16185575-G-T

http://identifiers.org/hco/7/GRCh38#41706839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#16185428-C-A

41706839-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16185428-C-G

41707274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16185004-A-G

41707777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16184525-A-G

41708260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 16184064-A-G

41708517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 16183811-C-T

41708679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16183703-T-C

41708705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16183679-A-G

41709018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 16183369-A-G

http://identifiers.org/hco/7/GRCh38#41709045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#16183339-C-A

41709045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 16183339-C-T

41709067-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16183234-A-T

41709075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16183226-G-T

41709147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16183140-G-T

41709149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16183138-C-T

41709453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16182826-T-C

41709628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16182673-G-A

41709863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16182438-T-C

41709863-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16182438-T-G

41710092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16182191-C-T

41710210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16182080-G-A

41710227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16182060-C-T

41710653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: non coding transcript exon variant
orthologous variants: 16181642-T-C

http://identifiers.org/hco/7/GRCh38#41710685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#16181611-C-A

41710685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: non coding transcript exon variant
orthologous variants: 16181611-C-T

41710695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: non coding transcript exon variant
orthologous variants: 16181601-A-G

http://identifiers.org/hco/7/GRCh38#41710736-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#16181561-C-A

41710983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 16181203-T-C

41711012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 16181175-T-C

41711062-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 16181135-C-G

41711158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 16181023-A-G

41711275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 16180905-A-G

41711402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 16180789-A-G

41711608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 16180668-T-C

41711934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 16180267-T-C

41712026-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 16180217-T-A

41712119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 16180136-T-C

41712123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 16180132-C-T

41712153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 16180110-A-G

41712267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 16179980-G-A

41712353-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 16179903-T-G

41712872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 16179768-G-A

41712896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 16179744-G-A

41712896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 16179744-G-T

41712968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 16179669-G-T

41713205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16179508-A-G

41713205-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16179508-A-T

41713220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16179494-G-A

41713227-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16179487-T-A

41713228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16179486-G-T

41713283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16179438-G-T

41713393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16179335-G-T

41713439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16179290-A-G

http://identifiers.org/hco/7/GRCh38#41713837-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#16179192-A-C

http://identifiers.org/hco/7/GRCh38#41714489-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#16179066-A-C

41714489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16179066-A-G

41714489-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16179066-A-T

41719130-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16171271-T-G

41719178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16171229-T-C

41719336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16171095-C-T

41719441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16171015-T-C

41719441-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16171015-T-G

41721582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16170617-T-C

41721844-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16170324-T-A

41721887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16170282-G-T

41722301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16169890-G-A

41722522-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16169675-A-T

41722612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16169602-T-C

http://identifiers.org/hco/7/GRCh38#41722669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#16169547-C-A

41724690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16168381-T-C

41724897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16168182-A-G

41724943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16168132-A-G

41725061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16168017-C-T

41725228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16167867-G-A

41725450-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16167645-C-G

41725450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16167645-C-T

41725474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16167621-T-C

41725588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16167520-A-G

41725839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16167211-T-C

41725915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16167041-A-G

41726019-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16166886-C-G

41726121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16166799-A-G

41726213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16166722-G-A

41726352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16166596-G-A

41726375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16166539-G-A

41726657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16166246-G-A

41726866-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16166084-T-A

41726961-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16165982-T-A

41727353-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16165597-G-C

41727409-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16165542-C-G

41727409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16165542-C-T

41727472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16165487-A-G

41727872-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16165101-A-T

41728030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16164959-G-A

41728070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16164919-T-C

41728850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16163878-G-A

http://identifiers.org/hco/7/GRCh38#41728892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#16163834-C-A

41728892-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16163834-C-G

41728894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16163832-C-T

41729051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16163430-C-T

41729518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16162978-G-A

http://identifiers.org/hco/7/GRCh38#41729862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#16162658-C-A

41729900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16162613-G-A

41730023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16162469-A-G

41730045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16162447-C-T

http://identifiers.org/hco/7/GRCh38#41730060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#16162432-C-A

41730158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16162340-G-T

41730181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16162317-A-G

http://identifiers.org/hco/7/GRCh38#41730442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#16161883-C-A

41730463-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16161862-T-G

41730738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16161545-G-T

41730769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16161519-C-T

41730884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16161405-A-G

http://identifiers.org/hco/7/GRCh38#41731109-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#16161233-A-C

41731144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16161205-C-T

http://identifiers.org/hco/7/GRCh38#41731200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#16161156-C-A

41731202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16161154-G-A

41731881-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16160990-T-A

41732063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16160828-T-C

41732138-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 16160760-T-G

41732434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 16160489-G-A

41732505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16160418-G-A

41732523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16160404-A-G

41732575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16160357-G-A

41732685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16160278-G-A

41733121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16159913-C-T

http://identifiers.org/hco/7/GRCh38#41733198-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#16159840-A-C

41733220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16159818-G-A

41733244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16159794-C-T

41733373-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16159678-A-T

41733398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16159659-G-T

41733429-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16159628-G-C

41733429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16159628-G-T

41733816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16159386-A-G

http://identifiers.org/hco/7/GRCh38#41734093-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#16159162-C-A

41734168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16159096-A-G

41734168-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16159096-A-T

41734316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16158929-G-A

41734355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16158873-C-T

http://identifiers.org/hco/7/GRCh38#41734666-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#16158409-A-C

41734666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16158409-A-G

41734753-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16158182-T-G

41735042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16157916-T-C

41735252-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16157695-G-C

41735331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16157618-T-C

41735509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16157076-T-C

41735840-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16156745-T-G

41735913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16156675-C-T

41736060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16156525-T-C

41736362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16156363-G-A

41736402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16156351-T-C

41736530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16156233-C-T

41736586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16156177-A-G

41736640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16156132-G-A

41736705-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16156118-C-G

http://identifiers.org/hco/7/GRCh38#41736835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#16156002-C-A

41736835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16156002-C-T

41736884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16155964-G-T

41736956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16155892-C-T

41737074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16155791-G-A

41737074-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16155791-G-C

41737103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16155764-A-G

41737115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16155750-C-T

41737322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16155555-G-A

41738007-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16155332-A-T

41738039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16155298-G-A

41738149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16155197-C-T

41738287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16155105-G-A

41738402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16154960-G-A

41738533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16154851-C-T

41738639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16154748-A-G

41739052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16154335-G-A

41739553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16153142-G-A

41739634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16153063-A-G

41739661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16153036-A-G

http://identifiers.org/hco/7/GRCh38#41739760-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#16152869-A-C

41739860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16152706-A-G

41739999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16152591-A-G

http://identifiers.org/hco/7/GRCh38#41740187-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#16152443-A-C

http://identifiers.org/hco/7/GRCh38#41740240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#16152394-C-A

41740240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16152394-C-T

41740254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16152380-T-C

41740340-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16152285-A-T

http://identifiers.org/hco/7/GRCh38#41763199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#16148185-C-A

41763199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16148185-C-T

41763259-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16148134-T-G

41763335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16148055-C-T

41763398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16148001-G-A

41763533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16147888-G-A

41763533-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16147888-G-C

41767199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16144258-C-T

http://identifiers.org/hco/7/GRCh38#41768657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#16134285-C-A

41768657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16134285-C-T

41768698-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16134244-T-G

http://identifiers.org/hco/7/GRCh38#41768724-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#16134217-A-C

41769247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16133730-C-T

41769325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16133651-G-T

http://identifiers.org/hco/7/GRCh38#41769395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#16133584-C-A

http://identifiers.org/hco/7/GRCh38#41769483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#16133502-C-A

41769483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16133502-C-T

41772216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16132782-G-A

41772245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16132751-G-A

41772267-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16132729-C-G