9758279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109886250-G-A

http://identifiers.org/hco/11/GRCh38#9758285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#109886256-C-A

9758287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109886258-C-T

9758292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109886263-G-A

9758292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109886263-G-T

http://identifiers.org/hco/11/GRCh38#9758490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#109886374-C-A

9758490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109886374-C-T

http://identifiers.org/hco/11/GRCh38#9758559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109886443-C-A

9758559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109886443-C-T

9758623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109886516-G-A

9758623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109886516-G-T

9758915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109886748-G-A

9759353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109887151-G-A

9759353-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109887151-G-C

9759353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109887151-G-T

9759373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109887171-T-C

9759470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109887273-G-A

9759470-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109887273-G-T

http://identifiers.org/hco/11/GRCh38#9759645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#109887410-C-A

9759645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109887410-C-T

9759665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109887429-C-T

9759686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109887452-C-T

9759795-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109887550-C-G

9759795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109887550-C-T

9760161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109887912-T-C

9760443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109888168-C-T

9761646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109891734-G-A

9761646-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109891734-G-C

9761724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109891810-G-A

9761993-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109892269-T-G

9762024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109892283-G-T

9764318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109894854-T-C

9765132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109895906-T-C

9765264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109896050-G-A

9765444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109896231-C-T

9766217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109896928-A-G

9766448-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109897131-C-G

http://identifiers.org/hco/11/GRCh38#9766841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109897319-C-A

9767327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109897670-A-G

9767345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109897686-C-T

9767540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109897824-C-T

9767617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109897886-C-T

9767622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109897891-G-A

9767654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109897920-C-T

9768135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109897998-G-A

9768193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109898053-C-T

9775173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109905533-T-C

9775428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109905716-A-G

9775486-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-G

9775496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109905770-G-A

9775496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109905770-G-T

9775682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109905937-G-A

9775682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109905937-G-T

http://identifiers.org/hco/11/GRCh38#9775702-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109905957-A-C

9775794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109906034-G-T

9775954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109906130-T-C

9776148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109906311-A-G

9776510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109906543-G-A

9778446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109906977-G-A

http://identifiers.org/hco/11/GRCh38#9778522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#109907038-C-A

9778562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109907062-G-T

http://identifiers.org/hco/11/GRCh38#9779417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#109907834-C-A

9779538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109907933-A-G

9779628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109907993-G-T

9779646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109907997-G-A

9779646-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109907997-G-C

9779646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109907997-G-T

9779768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109908095-T-C

9779768-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109908095-T-G

9779835-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109908127-C-G

http://identifiers.org/hco/11/GRCh38#9779860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#109908152-C-A

9779860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109908152-C-T

http://identifiers.org/hco/11/GRCh38#9779969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#109908254-C-A

9779969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109908254-C-T

9780011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109908293-G-T

9780129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109908386-G-A

9780223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109908460-G-A

9780223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109908460-G-T

http://identifiers.org/hco/11/GRCh38#9780225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#109908462-C-A

9780225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109908462-C-T

9780295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109908509-G-A

9780295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109908509-G-T

9780321-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109908536-T-A

9780321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109908536-T-C

9780430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109908617-G-A

9780442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109908629-G-T

9780541-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109908728-C-G

http://identifiers.org/hco/11/GRCh38#9782918-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#109910142-C-A

9783051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109910266-G-T

http://identifiers.org/hco/11/GRCh38#9783341-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#109910570-C-A

9783343-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109910572-C-G

9783984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109910995-T-C

9784255-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109911232-A-T

9784314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109911254-A-G

9784314-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109911254-A-T

9784905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109911762-A-G

http://identifiers.org/hco/11/GRCh38#9784976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#109911783-C-A

9785018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109911820-T-C

9785018-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109911820-T-G

9785070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109911857-G-T

9785098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109911874-C-T

http://identifiers.org/hco/11/GRCh38#9785136-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#109911894-A-C

9785137-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109911895-T-A

9785184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109911942-T-C

9785193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109911951-T-C

9785231-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109911989-T-A

9785238-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109911996-G-C

9785274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109912032-G-A

9785362-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109912123-T-A

9786330-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109912386-T-G

9787203-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109912758-T-A

9787525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109913081-T-C

9787585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109913133-C-T

9787588-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109913136-C-G

9787607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109913143-G-A

9787607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109913143-G-T

9787619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109913152-G-T

9787682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109913215-C-T

9787758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109913296-T-C

9787828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109913370-G-A

9787828-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109913370-G-C

9787882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109913396-T-C

9788252-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109913683-C-G

9788938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109914001-A-G

9788955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109914017-C-T

9788971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109914033-C-T

9788989-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109914050-A-T

http://identifiers.org/hco/11/GRCh38#9788997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#109914058-C-A

9788997-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109914058-C-G

http://identifiers.org/hco/11/GRCh38#9789157-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#109914228-A-C

http://identifiers.org/hco/11/GRCh38#9789382-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#109914456-A-C

9789412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109914486-C-T

9789657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109914637-G-A

9789801-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109914760-T-A

http://identifiers.org/hco/11/GRCh38#9790419-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#109915990-A-C

9790604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109916151-C-T

9790616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109916163-G-A

9790772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109916326-G-A

9790772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109916326-G-T

9790847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109916401-G-A

9790847-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109916401-G-C

9790850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109916404-A-G

9790876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109916416-G-T

9790895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109916432-T-C

9790969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109916478-T-C

http://identifiers.org/hco/11/GRCh38#9791005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#109916505-C-A

9791005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109916505-C-T

9791235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109916703-T-C

http://identifiers.org/hco/11/GRCh38#9791398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#109916961-C-A

9791540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109917098-T-C

9791969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109917443-G-A

9792133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109917589-C-T

9792513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109917661-A-G

9793824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109918417-C-T

http://identifiers.org/hco/11/GRCh38#9794731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#109918636-C-A

9794742-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109918647-T-G

http://identifiers.org/hco/11/GRCh38#9794744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#109918649-C-A

9794744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109918649-C-T

9795035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109918882-T-C

9795302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109919407-C-T

9795612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109919688-T-C

http://identifiers.org/hco/11/GRCh38#9795704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#109919785-C-A

9795704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109919785-C-T

9795786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109919836-G-T

9795802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109919851-A-G

9795984-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109920031-G-C

9795984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109920031-G-T

9796017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109920060-G-T

http://identifiers.org/hco/11/GRCh38#9796060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#109920101-C-A

9796060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109920101-C-T

http://identifiers.org/hco/11/GRCh38#9796084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#109920124-C-A

9796213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109920226-G-A

9796383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109920345-T-C

9797435-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109921088-T-A

9797435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109921088-T-C

9797455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109921108-C-T

9797612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109921188-C-T

9797734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109921406-A-G

9797778-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109921446-G-C

9797778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109921446-G-T

9797803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109921473-T-C

9798248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109922073-G-A

9798361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109922182-A-G

9801719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109923747-G-A

9801768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109923795-C-T

9801924-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109923946-T-A

9802029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109924050-T-C

9802031-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109924052-G-C

9802515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109925296-G-A

9802799-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109925568-T-G

9802810-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109925579-G-C

9803004-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109925771-C-G

9803067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109925825-T-C

9803133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109925890-A-G

9803293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109926174-C-T

http://identifiers.org/hco/11/GRCh38#9803479-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#109926504-A-C

9803489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109926514-C-T

9803641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109926646-G-A

9806347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109927702-G-A

9806720-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109928032-T-G

http://identifiers.org/hco/11/GRCh38#9806726-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#109928038-A-C

9806738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109928051-G-A

9806798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109928112-G-A

9806979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109928263-T-C

9807144-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109928393-C-G

9807150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109928399-G-A

9807227-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109928476-C-G

http://identifiers.org/hco/11/GRCh38#9807256-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#109928504-A-C

9807413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109928615-A-G

9807913-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109928918-C-G

9807913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109928918-C-T

9807954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109928929-G-T

http://identifiers.org/hco/11/GRCh38#9807959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#109928934-C-A

9807959-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109928934-C-G

9808114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 109929082-T-C

9808124-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 109929092-A-T

http://identifiers.org/hco/11/GRCh38#9808183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#109929151-C-A

9808393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109929354-T-C

http://identifiers.org/hco/11/GRCh38#9808425-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#109929386-A-C

9808522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109929461-G-A

9808588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109929531-C-T

9808626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109929572-C-T

http://identifiers.org/hco/11/GRCh38#9808628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#109929574-C-A

9808628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109929574-C-T

9808683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109929628-T-C

9808683-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109929628-T-G

9808690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109929635-G-A

9808690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109929635-G-T

9808710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109929655-G-T

http://identifiers.org/hco/11/GRCh38#9808714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#109929659-C-A

9808714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109929659-C-T

9808755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109929677-T-C

http://identifiers.org/hco/11/GRCh38#9808786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#109929710-C-A

9808850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109929766-C-T

9810504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109933186-C-T

http://identifiers.org/hco/11/GRCh38#9810553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#109933221-C-A

9810573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109933241-G-A

9810573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109933241-G-T

http://identifiers.org/hco/11/GRCh38#9810581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#109933249-C-A