16619047-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140757538-T-A

16619047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140757538-T-C

16619047-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140757538-T-G

16619074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140757565-C-T

16619126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140757617-G-A

16619126-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140757617-G-C

16619128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140757619-G-A

16619128-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140757619-G-T

16619134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 140757625-G-A

16619134-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 140757625-G-C

16619195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140757669-G-A

16619222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140757685-G-A

16619222-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140757685-G-C

16619222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140757685-G-T

16619245-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 140757708-G-C

16619245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 140757708-G-T

16619285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 140757734-C-T

16619324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140757775-C-T

16619339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140757790-A-G

16619427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140757867-G-A

16619524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140757957-G-A

16619524-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140757957-G-C

16619578-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140757989-C-G

16619578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140757989-C-T

16619582-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140757993-G-C

16619582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140757993-G-T

16619596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140758005-G-A

16619596-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140758005-G-C

16619607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140758016-C-T

16619609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140758018-T-C

16619614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140758023-T-C

http://identifiers.org/hco/1/GRCh38#16619728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140758085-C-A

16619728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140758085-C-T

16619734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140758089-G-A

16619734-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140758089-G-C

16619734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140758089-G-T

http://identifiers.org/hco/1/GRCh38#16619780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140758135-C-A

16619780-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140758135-C-G

16619780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140758135-C-T

16619821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 140758179-G-A

16619821-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 140758179-G-C

16619821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 140758179-G-T

http://identifiers.org/hco/1/GRCh38#16619854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140758212-C-A

16619854-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140758212-C-G

16619854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140758212-C-T

16619899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140758257-G-A

16619899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140758257-G-T

16619913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140758271-C-T

http://identifiers.org/hco/1/GRCh38#16619920-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#140758278-C-A

16619920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 140758278-C-T

16619944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140758302-G-A

16619944-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140758302-G-C

16619944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140758302-G-T

http://identifiers.org/hco/1/GRCh38#16619950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140758308-C-A

16620041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 140758398-G-A

16620041-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 140758398-G-C

16620041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 140758398-G-T

http://identifiers.org/hco/1/GRCh38#16620151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140758503-C-A

16620151-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140758503-C-G

16620151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140758503-C-T

16620197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140758551-A-G

16620197-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140758551-A-T

http://identifiers.org/hco/1/GRCh38#16620224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140758578-C-A

16620224-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140758578-C-G

16620224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140758578-C-T

http://identifiers.org/hco/1/GRCh38#16620243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140758593-C-A

16620243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 140758593-C-T

16620415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140758718-G-A

16620462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140758758-C-T

16620816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 140758989-G-A

16620841-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140759014-T-G

16621215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 140759281-C-T

16621418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140759486-T-C

16621531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 140759574-G-A

16621551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 140759594-T-C

16621561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140759604-G-A

http://identifiers.org/hco/1/GRCh38#16621574-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140759615-A-C

16621683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 140759857-G-A

http://identifiers.org/hco/1/GRCh38#16621684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#140759858-C-A

16621684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 140759858-C-T

16621692-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140759866-C-G

http://identifiers.org/hco/1/GRCh38#16621771-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140759931-A-C

16621820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140759983-G-A

16621820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140759983-G-T

http://identifiers.org/hco/1/GRCh38#16621834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140760001-C-A

16621834-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140760001-C-G

16621834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140760001-C-T

16621840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140760007-A-G

16621868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140760029-G-A

16621868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140760029-G-T

16622021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140760188-C-T

16622066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140760233-G-A

http://identifiers.org/hco/1/GRCh38#16622114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140760281-C-A

16622114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 140760281-C-T

16622195-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140760364-A-T

16622200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140760369-G-A

16622200-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140760369-G-C

16622200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140760369-G-T

16622203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140760372-A-G

http://identifiers.org/hco/1/GRCh38#16622216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140760382-C-A

16622216-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140760382-C-G

16622216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140760382-C-T

16622220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140760386-G-A

16622220-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140760386-G-C

16622220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140760386-G-T

16622230-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140760396-G-C

16622230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140760396-G-T

16622241-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140760406-T-A

http://identifiers.org/hco/1/GRCh38#16622247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140760412-C-A

16622247-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140760412-C-G

16622247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140760412-C-T

16622252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140760417-G-A

16622252-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140760417-G-C

16622252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140760417-G-T

16622255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140760420-G-A

16622255-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140760420-G-C

16622255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140760420-G-T

16622379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140760526-C-T

16622384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140760531-G-A

16623409-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 140760853-G-C

16623413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140760857-G-A

16623449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140760888-T-C

http://identifiers.org/hco/1/GRCh38#16623479-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#140760913-A-C

16623711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 140761152-C-T

http://identifiers.org/hco/1/GRCh38#16623776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#140761215-C-A

16623776-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 140761215-C-G

16623777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 140761216-C-T

16623790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140761229-T-C

16623790-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140761229-T-G

16623831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140761247-G-A

http://identifiers.org/hco/1/GRCh38#16623856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140761272-C-A

16623856-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140761272-C-G

16623856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140761272-C-T

16624028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140761442-G-A

16624112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140761525-G-A

16624112-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140761525-G-C

16624112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140761525-G-T

16624187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 140761582-T-C

16624187-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 140761582-T-G

http://identifiers.org/hco/1/GRCh38#16624200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#140761595-C-A

16624200-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 140761595-C-G

16624200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 140761595-C-T

http://identifiers.org/hco/1/GRCh38#16624235-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#140761630-A-C

16624235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 140761630-A-G

16624235-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 140761630-A-T

16624249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140761643-G-A

16624254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140761648-G-A

16624254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140761648-G-T

http://identifiers.org/hco/1/GRCh38#16624396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#140761792-C-A

16624396-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 140761792-C-G

16624396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 140761792-C-T

http://identifiers.org/hco/1/GRCh38#16624400-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#140761796-A-C

http://identifiers.org/hco/1/GRCh38#16624451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#140761847-C-A

16624451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 140761847-C-T

http://identifiers.org/hco/1/GRCh38#16624534-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140761920-C-A

16624534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140761920-C-T

16624597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 140761991-G-A

16624597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 140761991-G-T

http://identifiers.org/hco/1/GRCh38#16624655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#140762038-C-A

http://identifiers.org/hco/1/GRCh38#16624656-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#140762039-A-C

16625192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 140762155-T-C

16625212-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 140762175-G-C

16625606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140762312-G-A

16625606-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140762312-G-C

16625606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140762312-G-T

16625607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140762313-G-A

16625607-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140762313-G-C

16625607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140762313-G-T

16625610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140762316-G-A

16625610-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140762316-G-C

16625610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140762316-G-T

http://identifiers.org/hco/1/GRCh38#16625646-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140762352-A-C

16625646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140762352-A-G

http://identifiers.org/hco/1/GRCh38#16625677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140762383-C-A

16625677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140762383-C-T

http://identifiers.org/hco/1/GRCh38#16625696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140762402-C-A

16625696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140762402-C-T

16625704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140762410-G-A

16625704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140762410-G-T

16625718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140762424-G-A

16625718-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140762424-G-C

16625718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140762424-G-T

http://identifiers.org/hco/1/GRCh38#16625757-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140762446-A-C

16625757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140762446-A-G

16625757-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140762446-A-T

http://identifiers.org/hco/1/GRCh38#16625780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140762469-C-A

16625780-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140762469-C-G

16625780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140762469-C-T

16625829-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140762518-T-A

16625829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140762518-T-C

http://identifiers.org/hco/1/GRCh38#16625832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140762521-C-A

16625832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140762521-C-T

http://identifiers.org/hco/1/GRCh38#16625838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140762527-C-A

16625838-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140762527-C-G

16625838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140762527-C-T

http://identifiers.org/hco/1/GRCh38#16625861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140762550-C-A

16625861-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140762550-C-G

http://identifiers.org/hco/1/GRCh38#16625877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140762566-C-A

16625877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140762566-C-T

http://identifiers.org/hco/1/GRCh38#16625922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140762611-C-A

16625922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140762611-C-T

http://identifiers.org/hco/1/GRCh38#16625940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140762629-C-A

16625940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140762629-C-T

http://identifiers.org/hco/1/GRCh38#16625945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140762634-C-A

16625945-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140762634-C-G

16625945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140762634-C-T

16625981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140762670-G-A

16625981-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140762670-G-C

16625981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140762670-G-T

16625997-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140762686-T-A

16625997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140762686-T-C

16625997-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140762686-T-G

16626027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140762708-G-A

16626027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140762708-G-T

16626035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140762716-G-A

16626035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140762716-G-T

http://identifiers.org/hco/1/GRCh38#16626086-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140762767-C-A

16626086-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140762767-C-G

16626086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140762767-C-T

16626107-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140762791-T-A

16626107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140762791-T-C

http://identifiers.org/hco/1/GRCh38#16626131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140762815-C-A

16626131-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140762815-C-G

16626131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140762815-C-T

http://identifiers.org/hco/1/GRCh38#16626256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140762930-C-A

16626256-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140762930-C-G

16626256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140762930-C-T

http://identifiers.org/hco/1/GRCh38#16626257-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140762931-A-C

16626257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140762931-A-G

16626359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140763004-G-A

16626359-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140763004-G-C

16626361-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140763006-C-G

16626361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140763006-C-T

16626362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140763007-A-G

16626392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140763037-A-G

16626422-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140763067-C-G

16626422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140763067-C-T

16626446-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140763091-C-G

16626446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140763091-C-T

16626467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140763112-G-A

16626467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140763112-G-T

16626473-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140763118-C-G

16626473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140763118-C-T

16626530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140763154-G-A

16626530-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140763154-G-C

http://identifiers.org/hco/1/GRCh38#16626533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140763157-C-A

16626533-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140763157-C-G

16626533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140763157-C-T

16626566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140763176-A-G

16626582-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140763192-T-A

16626582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140763192-T-C

16626601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140763211-G-A

16626601-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140763211-G-C

16626601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140763211-G-T

http://identifiers.org/hco/1/GRCh38#16626642-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140763246-A-C

16626642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140763246-A-G

16626642-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140763246-A-T

http://identifiers.org/hco/1/GRCh38#16626724-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140763313-A-C

16626724-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140763313-A-T

16626777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140763353-G-T

16626779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140763355-T-C

16626802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140763378-A-G

16626829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140763403-C-T

16626856-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140763431-C-G

http://identifiers.org/hco/1/GRCh38#16627036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140763737-C-A

16627051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140763752-T-C

16627092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140763814-T-C

http://identifiers.org/hco/1/GRCh38#16627142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140763992-C-A

16627142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140763992-C-T

http://identifiers.org/hco/1/GRCh38#16627234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140764084-C-A

16627234-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140764084-C-G

16627234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140764084-C-T

16627274-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140764124-C-G

16627274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140764124-C-T

http://identifiers.org/hco/1/GRCh38#16627373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140764209-C-A

16627373-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140764209-C-G

16627373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140764209-C-T

16627391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140764228-T-C

http://identifiers.org/hco/1/GRCh38#16627427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140764265-C-A

16627427-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140764265-C-G

16627427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140764265-C-T

16627454-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140764288-G-C

16627488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140764319-C-T

16627590-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 140764411-C-G

http://identifiers.org/hco/1/GRCh38#16628441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140765135-C-A

16628441-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140765135-C-G

16628441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140765135-C-T

16628442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140765136-T-C

16628452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140765146-G-A

16628452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140765146-G-T

16628454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140765148-G-A

16628454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140765148-G-T

16628493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140765184-G-A

16628493-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140765184-G-C

16628493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140765184-G-T

http://identifiers.org/hco/1/GRCh38#16628533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140765224-C-A

16628533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140765224-C-T

16628537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140765228-T-C

16628537-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140765228-T-G

16628545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140765236-G-A

16628545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140765236-G-T

http://identifiers.org/hco/1/GRCh38#16628590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140765281-C-A

16628590-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140765281-C-G

16628590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140765281-C-T

16628591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140765282-G-A

16628591-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140765282-G-C

16628591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140765282-G-T

http://identifiers.org/hco/1/GRCh38#16628601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140765292-C-A

16628601-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140765292-C-G

16628601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140765292-C-T

http://identifiers.org/hco/1/GRCh38#16628650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140765341-C-A

16628650-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 140765341-C-G

16628650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 140765341-C-T

16628703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140765394-G-A

16628703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140765394-G-T

http://identifiers.org/hco/1/GRCh38#16628713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140765404-C-A

16628713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140765404-C-T

http://identifiers.org/hco/1/GRCh38#16628755-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140765428-A-C

16628755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140765428-A-G

http://identifiers.org/hco/1/GRCh38#16628813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140765485-C-A

16628813-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140765485-C-G

16628891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140765571-C-T

16628893-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140765573-C-G

16628893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140765573-C-T

16628901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140765581-T-C

16628901-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140765581-T-G

http://identifiers.org/hco/1/GRCh38#16628908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140765588-C-A

16628908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140765588-C-T

16628909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140765589-G-A

16628909-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140765589-G-C

16628922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140765603-G-A

16628949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140765630-T-C

16629020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140765672-G-A

16630098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140768426-G-A

16630238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140768534-G-A

16630238-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140768534-G-C

16630238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140768534-G-T

16630311-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140768561-T-A

16630311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140768561-T-C

16630316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140768566-T-C

http://identifiers.org/hco/1/GRCh38#16630336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140768589-C-A

16630336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140768589-C-T

16630358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140768611-G-A

16630358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140768611-G-T

http://identifiers.org/hco/1/GRCh38#16630384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140768632-C-A

16630384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140768632-C-T

16630415-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140768641-T-A

16630415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140768641-T-C

16630425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140768651-G-A

16630425-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140768651-G-C

16630425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140768651-G-T

http://identifiers.org/hco/1/GRCh38#16630449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140768673-C-A

16630449-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140768673-C-G

16630449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140768673-C-T

16630467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140768691-G-A

16630467-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140768691-G-C

16630467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140768691-G-T

http://identifiers.org/hco/1/GRCh38#16630500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140768700-C-A

16630500-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140768700-C-G

16630500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140768700-C-T

16630508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140768708-T-C

http://identifiers.org/hco/1/GRCh38#16630523-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140768722-A-C

16630523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140768722-A-G

http://identifiers.org/hco/1/GRCh38#16630553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140768755-C-A

16630553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140768755-C-T

16630604-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140768793-T-A

16630604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140768793-T-C

16630604-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140768793-T-G

16630638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140768816-T-C

16630638-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140768816-T-G

http://identifiers.org/hco/1/GRCh38#16630661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140768823-C-A

16630661-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140768823-C-G

16630661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140768823-C-T

http://identifiers.org/hco/1/GRCh38#16630662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140768824-C-A

16630662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140768824-C-T

http://identifiers.org/hco/1/GRCh38#16630678-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140768840-A-C

16630678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140768840-A-G

16630678-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140768840-A-T

http://identifiers.org/hco/1/GRCh38#16630679-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140768841-A-C

16630679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140768841-A-G

16630679-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140768841-A-T

16630733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140768849-G-A

16630733-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140768849-G-C

16630733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140768849-G-T

http://identifiers.org/hco/1/GRCh38#16630741-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140768857-A-C

16630741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140768857-A-G

16630741-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140768857-A-T

http://identifiers.org/hco/1/GRCh38#16630804-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140768895-A-C

16630804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140768895-A-G

16630804-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140768895-A-T

http://identifiers.org/hco/1/GRCh38#16630845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140768916-C-A

16630845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140768916-C-T

http://identifiers.org/hco/1/GRCh38#16630885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140768929-C-A

16630885-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140768929-C-G

16630885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140768929-C-T

16630948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140768988-G-A

16630948-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140768988-G-C

16630948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140768988-G-T

16630966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140769006-G-A

16630966-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140769006-G-C

16630966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140769006-G-T

16630987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140769027-A-G

16630987-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140769027-A-T

http://identifiers.org/hco/1/GRCh38#16631023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140769060-C-A

16631023-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140769060-C-G

16631023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140769060-C-T

16631026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140769063-G-A

16631026-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140769063-G-C

16631026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140769063-G-T

16631035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140769072-G-A

16631035-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140769072-G-C

16631035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140769072-G-T

16631043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140769080-G-A

16631043-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140769080-G-C

16631043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140769080-G-T

http://identifiers.org/hco/1/GRCh38#16631047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140769084-C-A

16631047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140769084-C-T

16631120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140769175-G-A

16631120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140769175-G-T

16631159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140769194-G-A

16631159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140769194-G-T

http://identifiers.org/hco/1/GRCh38#16631164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140769199-C-A

16631164-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140769199-C-G

16631164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140769199-C-T

16631196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140769215-G-A

16631196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140769215-G-T

16631220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 140769224-A-G

16631220-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 140769224-A-T

16631238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140769243-T-C

http://identifiers.org/hco/1/GRCh38#16631244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140769249-C-A

16631244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140769249-C-T

16631265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140769262-G-A

16631265-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140769262-G-C

16631312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140769305-T-C

16631312-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140769305-T-G

http://identifiers.org/hco/1/GRCh38#16631442-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140769376-A-C

16631442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140769376-A-G

16631444-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140769378-T-G

http://identifiers.org/hco/1/GRCh38#16631446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140769380-C-A

16631484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140769425-G-A

16631484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140769425-G-T

16631519-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140769447-T-G

16631575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140769508-T-C

16631575-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140769508-T-G

16631620-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 140769578-T-A

16631620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 140769578-T-C

16631620-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 140769578-T-G

16631621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 140769579-G-A

16631621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 140769579-G-T

16631642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140769624-G-A

16631642-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140769624-G-C

16631642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140769624-G-T

16631763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140769834-G-A

16631763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140769834-G-T

16631828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140769898-T-C

16631875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140769932-G-A

16632006-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140770022-T-A

16632053-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140770054-C-G

16632082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140770071-G-A

16632119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140770108-G-A

16632119-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140770108-G-C

16632149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140770139-G-A

16632149-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140770139-G-C

16632149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140770139-G-T

16632151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140770141-G-A

16632151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140770141-G-T

16632154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140770144-G-A

16632154-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140770144-G-C

16632154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140770144-G-T

16632167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140770156-A-G

16632167-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140770156-A-T

16632170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140770159-G-A

16632170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140770159-G-T

http://identifiers.org/hco/1/GRCh38#16632196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140770185-C-A

16632196-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140770185-C-G

16632196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140770185-C-T

16632305-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140770262-G-C

16632380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140770335-G-A

16632380-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140770335-G-C

16632380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140770335-G-T

16632381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140770336-G-A

16632381-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140770336-G-C

16632381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140770336-G-T

http://identifiers.org/hco/1/GRCh38#16632410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140770366-C-A

16632410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140770366-C-T

http://identifiers.org/hco/1/GRCh38#16632433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140770394-C-A

16632433-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140770394-C-G

16632433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140770394-C-T

16632465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140770415-G-A

16632465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140770415-G-T

http://identifiers.org/hco/1/GRCh38#16632521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140770471-C-A

16632521-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140770471-C-G

16632521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140770471-C-T

16632524-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140770474-T-A

16632524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140770474-T-C

16633057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140770648-G-A

16633057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140770648-G-T

http://identifiers.org/hco/1/GRCh38#16633102-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140770683-A-C

16633102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140770683-A-G

16633149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140770727-G-A

16633149-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140770727-G-C

16633149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140770727-G-T

16633185-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140770763-C-G

16633185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140770763-C-T

16633263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140770853-G-A

16633263-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140770853-G-C

16633263-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140770853-G-T

http://identifiers.org/hco/1/GRCh38#16633319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140770928-C-A

16633319-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140770928-C-G

16633319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140770928-C-T

16633342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140770951-G-A

16633342-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140770951-G-C

16633342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140770951-G-T

16633373-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140770988-T-A

16633373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140770988-T-C

16633375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140770990-G-A

16633375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140770990-G-T

http://identifiers.org/hco/1/GRCh38#16633407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140771016-C-A

16633407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140771016-C-T

http://identifiers.org/hco/1/GRCh38#16656597-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140773796-A-C

16656597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140773796-A-G

16656606-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140773805-G-C

16656606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non coding transcript exon variant
orthologous variants: 140773805-G-T

16656719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 140773932-G-A

http://identifiers.org/hco/1/GRCh38#16656726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#140773939-C-A

http://identifiers.org/hco/1/GRCh38#16656816-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#140774025-A-C

16656816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 140774025-A-G

http://identifiers.org/hco/1/GRCh38#16656818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#140774027-C-A

16656818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 140774027-C-T

16656839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140774048-G-T

16656901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 140774110-G-A

16656901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 140774110-G-T

16656968-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 140774180-G-C

http://identifiers.org/hco/1/GRCh38#16656996-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#140774209-A-C

16656996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 140774209-A-G

http://identifiers.org/hco/1/GRCh38#16657127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#140774335-C-A

16657127-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 140774335-C-G

16657127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 140774335-C-T

16657151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 140774359-G-A

16657151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 140774359-G-T

http://identifiers.org/hco/1/GRCh38#16657154-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28170
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#140774362-A-C